Advances in molecular imaging and targeted therapeutics for lymph node metastasis in cancer: a comprehensive review

Abstract

Lymph node metastasis is a critical indicator of cancer progression, profoundly affecting diagnosis, staging, and treatment decisions. This review article delves into the recent advancements in molecular imaging techniques for lymph nodes, which are pivotal for the early detection and staging of cancer. It provides detailed insights into how these techniques are used to visualize and quantify metastatic cancer cells, resident immune cells, and other molecular markers within lymph nodes. Furthermore, the review highlights the development of innovative, lymph node-targeted therapeutic strategies, which represent a significant shift towards more precise and effective cancer treatments. By examining cutting-edge research and emerging technologies, this review offers a comprehensive overview of the current and potential impact of lymph node-centric approaches on cancer diagnosis, staging, and therapy. Through its exploration of these topics, the review aims to illuminate the increasingly sophisticated landscape of cancer management strategies focused on lymph node assessment and intervention.

Graphical Abstract

Introduction

Cancer continues to be a formidable health issue, partly due to its primary growths and its propensity to disperse to far-off parts of the body [1]. A frequent and vital area for such spread is the lymph nodes [2]. The spread of cancer to lymph nodes greatly influences the outcome and treatment approaches for those afflicted by cancer [3]. The spread of cancer to lymph nodes is a critical sign of the cancer's advancement and aggressiveness [4]. When cancer cells detach from the original tumor and move to the lymph nodes, it marks a critical phase in the cancer's development and plays a major role in determining the cancer stage [5]. This spread to lymph nodes can greatly affect the complexity of treatment strategies and is usually associated with a less favorable outcome [6]. Therefore, it's essential to comprehend how cancer spreads to lymph nodes to effectively combat the disease [7]. Advancements in imaging at the molecular level have transformed cancer detection and monitoring [8]. These sophisticated techniques provide in-depth understanding of cancer cell behavior in lymph nodes at both molecular and cellular levels [9]. Concurrently, specialized treatments have become crucial in contemporary cancer treatment [10]. These treatments focus on attacking cancer cells directly, aiming to minimize the adverse effects typically associated with conventional chemotherapy, thereby enhancing the overall results for patients [11].

Nanobiotechnology is leading the way in modern scientific advancements [12]. It plays a crucial role in the field of oncology, especially in addressing the spread of cancer to lymph nodes [13]. The use of tiny particles and advanced drug delivery systems at the nanoscale level presents innovative methods for accurately targeting cancer cells that have metastasized [14]. These approaches improve the effectiveness and safety of cancer therapies [15]. As this technology continues to develop quickly, it is paving new avenues for both the diagnosis and treatment of cancer [16].

The primary objective of this review is to provide a comprehensive analysis of the recent advancements in molecular imaging and targeted therapeutics, with a special emphasis on their application to lymph node metastasis in cancer. We aim to elucidate the current state of research and development in these areas, highlighting the role of nanobiotechnology in advancing cancer treatment. Through this review, we hope to offer insights into how these evolving technologies are shaping the future of cancer diagnosis, staging, and therapy, ultimately contributing to the improvement of patient outcomes in oncology.

Lymph node metastasis in relationship to its anatomy and physiology

Lymph nodes (LN) are strategically organized to facilitate their crucial role in the immune system [17]. Figure 1 illustrates the molecular processes involved in the spread of cancer to lymph nodes. Each LN is encapsulated in a fibrous capsule and internally structured into cortex, paracortex, and medulla regions [18]. Identify the commonly affected lymph nodes for each cancer type. The capsule extends trabeculae into the node, creating compartments. Lymph enters through afferent lymphatic vessels into the subcapsular sinus, traverses through the cortex and medulla, and exits via efferent lymphatic vessels. This flow ensures that lymph is exposed to various immune cells within the LN [19]. Figure 2 presents a detailed anatomical depiction of the structural features of lymph nodes. The cortex contains germinal centers with follicular dendritic cells (DCs) and B cells, vital for antibody production and B cell maturation [20]. The paracortex, rich in T cells and antigen-presenting DCs, is crucial for T cell activation [21]. The high endothelial venules (HEVs) in this region facilitate the entry of lymphocytes from the bloodstream into the LN, ensuring a continuous supply of immune cells [22]. The medulla contains macrophages and plasma cells, essential for antigen presentation and antibody secretion, respectively [23]. The structural organization, with distinct zones for different immune functions, ensures efficient immune surveillance and response [24]. Genes and factors play a crucial role in the structure and function of LN, which are integral components of the immune system [25]. CD34 and GLYCAM1 are particularly significant as they are expressed in high endothelial venules (HEVs) cells, facilitating the migration of lymphocytes into the lymph nodes [26]. Chemokines such as CCL19 and CCL21 are essential in guiding T cells to the paracortex area of the lymph nodes, a region crucial for T cell activation and differentiation [27]. CXCL13 plays a pivotal role in directing B cells to follicular areas, which are vital for B cell maturation and antibody production [28]. Lymphotoxin, another key factor, is involved in the development and maintenance of lymphoid structures, ensuring the proper architecture and function of the lymph nodes [29]. Additionally, adhesion molecules like VCAM-1 and ICAM-1 are critical for cell–cell interactions within the lymph nodes [30]. These molecules facilitate the binding of lymphocytes to other cells, aiding in the immune response coordination and the establishment of an effective immune surveillance system within the LN [31].

Fig. 1

The structural features of lymph nodes. It includes lymphatic endothelial cells (LEC) and fibroblastic reticular cells (FRC). Re-printed from the Springer Nature [89]

Fig. 2

The molecular processes involved in the spread of cancer to lymph nodes. Re-printed from the Springer Nature [89]

Fibroblastic reticular cells (FRCs) play a pivotal role in the structural and functional integrity of LN [32]. As specialized fibroblasts, they form a scaffold that defines the microenvironment within LN [33]. This framework supports the distinct niches for immune cells, facilitating efficient immune responses [34]. FRCs produce extracellular matrix (ECM) proteins, creating a three-dimensional network [35]. This network not only provides structural support but also acts as a conduit system, allowing for the transport of lymph, antigens, and other molecules throughout the LN [36]. This system is crucial for monitoring the status of draining peripheral tissues and for distributing antibodies produced within the LN [37]. FRCs are diverse, including T cell zone FRCs (TRCs), follicular DCs (fDCs), marginal reticular cells (MRCs), and medullary FRCs (medRCs) [38]. Each subtype is localized to specific LN areas, releasing a range of ligands, chemokines, and cytokines [39]. These molecules are vital for maintaining LN homeostasis and facilitating the appropriate immune responses [40]. FRCs, integral to the lymphatic system's architecture and immune response, express a variety of key genes and factors vital for their function [41]. CXCL12 and CCL19, chemokines secreted by FRCs, play a pivotal role in guiding the migration of T cells and dendritic cells, facilitating efficient immune surveillance and response [42]. Additionally, FRCs produce crucial cytokines such as IL-7 and IL-15, which are essential for T cell survival and maintaining homeostasis within the immune system [43]. RANKL and TRANCE are also significant, involved in lymph node organogenesis, underscoring their importance in the development and functional maintenance of FRCs [44]. Podoplanin, another critical component expressed in FRCs, is indispensable for their development and in maintaining the structure of the lymph nodes [45]. Lastly, VEGF-A contributes to the formation of lymphatic vessels associated with FRCs, highlighting its role in the lymphatic system's structural integrity and function [46]. Collectively, these genes and factors underscore the multifaceted role of FRCs in immune regulation and lymph node physiology [47]. Table 1 summarizes the primary pathways and mechanisms through which different types of cancer metastasize to lymph nodes.

Table 1 Overview of lymph node metastasis mechanisms in cancer

High endothelial venules (HEVs) are specialized blood vessels in LN, crucial for the recruitment of lymphocytes from the blood into the LN [48]. These cuboidal or columnar endothelial cells differ from typical flat venular endothelial cells, providing a unique environment for lymphocyte transmigration [49]. HEVs are primarily located in the paracortical area of the LN [50]. They express a variety of adhesion molecules and chemokines that facilitate the binding and extravasation of lymphocytes [51]. This selective recruitment is essential for the immune surveillance function of LN, ensuring a constant influx of naïve and memory lymphocytes for antigen recognition and initiation of adaptive immune responses [52]. HEVs are specialized blood vessels found predominantly in the lymph nodes and are crucial for the regulation of lymphocyte trafficking [53]. Key genes and factors contributing to the function of HEVs include several adhesion molecules and chemokines [54]. CD34 and GlyCAM-1, particularly in mice, are adhesion molecules present on HEVs that facilitate the initial binding of lymphocytes [55]. PNAd, a carbohydrate ligand on HEVs, interacts with L-selectin on lymphocytes, aiding in the lymphocyte's journey to the lymph node (LN) [56]. Additionally, chemokines such as CCL21 and CCL19 play a pivotal role in guiding lymphocytes into the LN via HEVs [57]. These chemokines create a gradient that directs the lymphocytes to their appropriate location within the lymph node [58]. Moreover, ICAM-1 and VCAM-1 are integral for the firm adhesion of lymphocytes to HEVs, a critical step before the lymphocytes transmigrate into the lymph node [59]. Lastly, Sphingosine-1-phosphate (S1P) is involved in regulating lymphocyte egress from LN through HEVs [60]. This complex interplay of molecules ensures that lymphocytes are efficiently circulated through the body, allowing for effective immune surveillance and response [61].

Lymphatic sinuses are a crucial component of LN, acting as channels through which lymph flows and is filtered [62]. The sinuses are lined with lymphatic endothelial cells (LECs) and are interconnected, ensuring a thorough screening of lymph [63].

The subcapsular sinus, located just beneath the capsule, receives lymph from afferent lymphatic vessels [64]. It allows the lymph to percolate slowly, exposing it to macrophages and dendritic cells that filter and sample the antigenic material [65]. The trabecular sinuses, extending from the subcapsular sinus into the LN, further facilitate the spread of lymph [66]. The medullary sinuses, located in the medulla, are rich in macrophages and plasma cells [67]. They play a role in the final stages of lymph filtration and antibody release into the lymph before it exits through the efferent lymphatic vessels [68]. The function and formation of lymphatic sinuses are influenced by a complex interplay of genes and factors that are crucial for their development and maintenance [69]. LYVE-1, a marker of Lymphatic Endothelial Cells (LECs), plays a significant role in lymphatic sinus formation and function, acting as a pivotal component in the structural and functional integrity of the lymphatic system [70]. CCL21, another vital factor produced by LECs, is instrumental in attracting CCR7-expressing cells into the sinuses, thereby facilitating immune surveillance and lymphatic flow [71]. Prox1, a transcription factor, is essential for the development of LECs, underscoring its fundamental role in the genesis and functionality of the lymphatic system [72]. Vascular Endothelial Growth Factor Receptor-3 (VEGFR-3) is involved in lymphangiogenesis, which is the formation of new lymphatic vessels, and it also maintains the integrity of lymphatic endothelial cells [73]. Lastly, Angiopoietin-2 plays a crucial role in regulating the remodeling and function of lymphatic sinuses, ensuring their proper structure and efficient operation in the lymphatic system [74]. Together, these factors and genes orchestrate the delicate balance necessary for the optimal functioning of lymphatic sinuses, which are integral to the lymphatic system and overall immune response [75].

The medullary region of LN plays a vital role in the immune response [76]. It is comprised of medullary cords and sinuses, populated with plasma cells, macrophages, and other immune cells [77]. The medullary cords are rich in antibody-producing plasma cells, essential for the humoral immune response [78]. Macrophages in the medullary sinuses phagocytose and process antigens, contributing to the antigen presentation and the activation of adaptive immunity [79]. This region is pivotal for the final stages of lymph filtration. It ensures that antigens are effectively presented to immune cells and that antibodies produced are released into the lymph before it exits the LN [80]. The arrangement facilitates efficient interaction between antigen-presenting cells and lymphocytes, crucial for a coordinated immune response [81]. The medulla, a critical region within lymphoid organs, relies on various key genes and factors for its proper function [82]. Among these, the J-chain and IgA/IgM play a crucial role in the polymerization of antibodies produced by plasma cells, enhancing the immune response [83]. The chemokine CXCL12 is instrumental in attracting plasma cells to the medullary cords, a process essential for the organization and function of the immune cells within the medulla [84]. FDC-M1, a specific marker for follicular dendritic cells in the medulla, is involved in the complex process of antigen presentation, a vital step in the initiation of adaptive immune responses [85]. Similarly, CD68 serves as a marker for macrophages located in the medullary sinuses, indicating the presence of these vital immune cells that are involved in phagocytosis and antigen presentation [86]. Lastly, MAdCAM-1 plays a key role in the homing of lymphocytes to the medullary region, ensuring the proper trafficking and localization of these critical immune cells [87]. Together, these factors and genes orchestrate the intricate functions of the medulla, underpinning the adaptive immune response [88].

Advances in molecular imaging for lymph node metastasis

Molecular imaging techniques for detecting lymph node metastasis represent a fusion of advanced technology and biological insights, offering detailed views and analyses of biological processes at the molecular and cellular levels in living organisms [115]. Among these techniques, Positron Emission Tomography (PET) is notable for its use of radiotracers like fluorodeoxyglucose (FDG), which are preferentially taken up by metabolically active cancer cells, allowing for their detection on scans [116]. Magnetic Resonance Imaging (MRI), particularly through its Diffusion-weighted imaging (DWI) variant, leverages magnetic fields and radio waves to produce detailed internal body structures, effectively identifying changes in tissue density and cellularity indicative of metastasis [117]. Computed Tomography (CT) scans, utilizing a series of X-ray images from various angles, provide comprehensive cross-sectional views of the body, aiding in the assessment of metastatic lymph nodes' size and location [118]. Ultrasound imaging, especially when combined with contrast agents, uses high-frequency sound waves to enhance the visualization of vascular patterns within lymph nodes, improving metastasis detection [119]. Lastly, Optical Imaging Techniques, including near-infrared fluorescence imaging, employ specific dyes absorbed by cancerous cells, rendering them visible under special lighting conditions [120]. These diverse methods collectively enhance the precision and effectiveness of lymph node metastasis detection, marking a significant advancement in medical imaging and cancer diagnosis [121]. Table 2 includes the advantages and limitations of each technique, providing a more comprehensive understanding of their roles in the detection and assessment of lymph node metastasis.

Table 2 Comparison of molecular imaging techniques for detecting lymph node metastasis

Sentinel lymph node biopsy (SLNB) is widely recognized for its remarkable sensitivity, being capable of detecting even a single cancer cell in sentinel lymph nodes. This makes it an essential tool in cancer staging and treatment planning. Its ability to identify cancer cells with such precision has made SLNB a cornerstone in guiding surgical and therapeutic decisions in cancer management [121,122,123,124,125,126,127,128]. However, recent advancements in molecular and nanoparticle technologies offer promising complementary benefits that could potentially surpass the capabilities of SLNB. Molecular techniques, such as polymerase chain reaction (PCR) and next-generation sequencing (NGS), provide highly specific and quantitative insights into cancer cell markers at both the genetic and epigenetic levels [129]. These methods enable earlier detection and more precise characterization of cancer cells, offering a deeper understanding of the tumor's molecular profile. This enhanced level of detail can contribute to more accurate diagnoses and tailored treatment strategies [130]. Nanoparticle technology further enhances detection sensitivity and specificity by allowing the targeted delivery of imaging agents or therapeutic compounds directly to cancer cells. This targeted approach has the potential to identify malignancies at an even earlier stage than SLNB, thereby improving early intervention opportunities. Additionally, nanoparticle-based techniques may facilitate non-invasive or minimally invasive procedures, which can significantly reduce patient discomfort and associated risks [131]. While SLNB remains a highly sensitive and valuable technique, integrating molecular and nanoparticle technologies holds the potential to revolutionize cancer diagnosis and treatment. These cutting-edge approaches not only offer more detailed molecular profiling but also enhance imaging capabilities and provide targeted treatment options, leading to a comprehensive and personalized approach to cancer management. By combining the strengths of SLNB with these advanced technologies, there is a promising avenue for improving diagnostic accuracy and therapeutic outcomes for cancer patients [132].

Nanobiotechnology in molecular imaging

Nanobiotechnology, a field that merges nanotechnology with biology, has significantly advanced the detection of lymph node metastasis in cancer patients. This advancement is critical because early detection of metastasis can dramatically improve treatment outcomes [127]. Table 3 compares the various nanobiotechnology tools used in molecular imaging of lymph node metastasis. One of the key ways nanobiotechnology aids in this detection is through the development of nanoparticle-based contrast agents used in molecular imaging [128]. These agents, often tagged with fluorescent dyes or radioactive isotopes, enhance the visibility of cancer cells in imaging techniques such as PET, MRI, and CT scans [129]. For example, gold nanoparticles (AuNPs) are used for their excellent photothermal properties and bio-compatibility. Quantum dots (QDs), another type, are semiconductor nanoparticles that provide high fluorescence and stability, making them ideal for long-term imaging [130]. Liposomes, dendrimers, and carbon nanotubes are also used, each offering unique properties that aid in targeted imaging. The effectiveness of these nanoparticles can be further enhanced by attaching specific molecules that target cancer markers [131]. For instance, attaching antibodies against HER2/neu to nanoparticles can specifically target breast cancer cells. Similarly, using molecules that target the VEGF gene helps in identifying tumors with angiogenesis [132]. Figure 3 discusses recent research focusing on nanovectors made from gold and magnetic materials for the purpose of delivering genes in melanoma.

Table 3 Comparison of nanobiotechnology tools in molecular imaging

Fig. 3 

Recent advancements in the use of gold-based and magnetic-based nanovectors for delivering genes in melanoma. A The first approach involves the transdermal delivery of plasmid DNAs encoding a microRNA-221 inhibitor gene (Mi221) using AuPT nanoparticles for the treatment of cutaneous melanoma. This method is depicted schematically. The source of this information is credited to Shahbazi et al. in 2016, with permission from the American Chemical Society [133]. B, i The second approach involves the local injection of gene carriers based on magnetic nanoparticles (MNP), followed by external magnetic attraction. This technique ensures efficient and long-term gene delivery. The source of this information is attributed to Borroni et al. in 2017, with permission from Elsevier [134]. B, ii Within the same study by Borroni et al. in 2017, there is also mention of green fluorescent protein (GFP) expression in tumors after in situ injection of lentiviral vectors combined with magnetic nanoparticles (LV-MNPs). This demonstrates the effectiveness of this approach in gene delivery, also with permission from Elsevier [134]

While normal imaging agents offer a more general approach to cancer detection, they often fall short in terms of specificity and precision, especially in lymph node detection [130]. Nanoparticles, with their enhanced targeting capabilities, and quantum dots, with their exceptional sensitivity and specificity, provide more advanced options for the detection of cancer in lymph nodes, greatly improving the accuracy of cancer staging and treatment planning [131, 132].

The size of imaging agents plays a crucial role in determining their effectiveness, particularly in the detection of lymph node metastasis. “Normal” imaging agents typically consist of molecules or small particles ranging from a few nanometers to micrometers in size [133]. These agents are widely used in traditional imaging techniques such as PET, MRI, and CT scans. While they are capable of identifying metabolically active cancer cells, they often lack specificity, making them less effective in accurately targeting cancer cells within the lymph nodes. Their distribution within tissues is relatively straightforward, but the general nature of these imaging agents means they may not offer the precise detection needed for early identification of metastasis in lymph nodes [134].

Nanoparticles, on the other hand, are engineered to be within the nanometer range, typically between 1 and 100 nm. Their smaller size allows for enhanced targeting capabilities and the potential for multifunctionality through surface modifications [134]. For instance, gold nanoparticles are used as contrast agents in CT imaging, providing excellent visibility of cancer cells, while magnetic nanoparticles are effective in enhancing MRI contrast [135]. The ability to modify the surfaces of these nanoparticles means they can be tailored to target specific cancer cells within the lymph nodes, significantly improving their utility in detecting metastasis. This targeted approach allows for more accurate identification and assessment of cancer spread, making nanoparticles a promising tool in lymph node imaging [136].

Quantum dots represent an even more advanced imaging agent, with sizes typically ranging from 2 to 10 nm. These semiconductor nanoparticles have unique optical properties, such as size-tunable fluorescence, which makes them highly sensitive and specific in detecting cancer biomarkers [137]. Their high brightness and stability make them exceptionally well-suited for long-term imaging applications. When conjugated with targeting molecules such as antibodies or peptides, quantum dots can specifically bind to cancer cells, providing precise molecular imaging at the nanoscale. This specificity and sensitivity make them particularly effective for detecting cancer in lymph nodes, offering unparalleled accuracy compared to normal imaging agents and nanoparticles [139].

Recent advancements in nanotechnology have significantly enhanced the specificity and sensitivity of nanoparticles as contrast agents for detecting lymph node metastasis [159]. One approach is the functionalization of nanoparticles with ligands or antibodies that bind to specific tumor markers, improving targeting accuracy [160]. For instance, nanoparticles coated with antibodies against the PDL1 gene can specifically target tumor cells that evade immune detection [161]. Surface modifications with polyethylene glycol (PEG) have improved circulation time and reduced immunogenicity [162]. Dual-modality nanoparticles, combining two different imaging modalities, like PET/MRI, provide comprehensive information about the tumor environment [163]. Advances in genes like RAS, MYC, BCL2, which are involved in cell proliferation, apoptosis, and survival, aid in the development of targeted therapies [164]. Additionally, smart nanoparticles that respond to tumor microenvironment factors like pH or enzymatic activity are being developed, enhancing specificity in detecting metastasis involving genes like CASP8 (involved in apoptosis) and MET (associated with cell scattering and invasion) [165].

While nanobiotechnology in molecular imaging presents groundbreaking potential for detecting lymph node metastasis, several challenges and limitations exist [166]. One major challenge is the potential toxicity and biocompatibility of nanoparticles [167]. For instance, some metal-based nanoparticles, like silver nanoparticles, may pose toxicity risks to healthy cells and organs [168]. This necessitates extensive research and testing to ensure their safe application in clinical settings [169]. Another limitation is the efficient delivery and targeting of these nanoparticles to the tumor sites [170]. Achieving precise targeting is crucial to avoid non-specific distribution, which can lead to false positives or negatives in imaging [171]. For example, nanoparticles might accumulate in organs like the liver or spleen, leading to imaging artifacts [172].

One significant challenge is the potential toxicity and biocompatibility of nanoparticles, which is being addressed through the development of biodegradable materials and surface modifications [173]. Another issue is the efficient and targeted delivery of nanoparticles to tumor sites, which involves understanding and targeting cancer-specific markers and pathways, such as NOTCH (involved in cell differentiation) and WNT (associated with cell proliferation and migration) [174]. Overcoming the body's immune response is another hurdle, necessitating the design of stealth nanoparticles that can evade the immune system [175]. Research is also focused on optimizing the size, shape, and surface charge of nanoparticles to improve their lymph node targeting ability and minimize off-target effects [176]. Furthermore, addressing the heterogeneity of tumors, which involves genes like PTEN (tumor suppressor) and PIK3CA (involved in cell growth), is crucial for effective treatment [177].

The size, shape, and surface chemistry of nanoparticles play a significant role in their distribution and elimination from the body [178]. For instance, smaller nanoparticles might be quickly cleared from the body, reducing their effectiveness, while larger ones might accumulate in unintended areas [179]. Additionally, the cost of developing and manufacturing these advanced nanomaterials can be high, limiting their accessibility and widespread use [180]. The process involves complex synthesis and often requires specialized equipment and expertise [181]. Lastly, regulatory hurdles for approval of new nanomaterials for clinical use are significant [182]. Each new nanoparticle formulation must undergo rigorous testing and approval processes to ensure safety and efficacy, which can be time-consuming and resource-intensive [183].

Quantum dots in imaging

Quantum dots (QDs) significantly improve the imaging of lymph node metastases due to their unique optical properties [184]. QDs are nanoscale semiconductor particles that exhibit size-tunable fluorescence, meaning their emission wavelength can be adjusted based on their size [185]. This feature allows for the simultaneous imaging of multiple biological targets using different colored QDs [186]. For instance, CdSe/ZnS QDs can be used for deep tissue imaging due to their near-infrared fluorescence [187]. When conjugated with targeting molecules such as antibodies or peptides, QDs can specifically bind to cancer cells [188]. Genes like HER2, VEGF, EGFR, MMP-9, and PSMA are often overexpressed in cancerous tissues and can be targeted by these conjugated QDs [189]. HER2 is involved in cell growth and differentiation, VEGF in angiogenesis, EGFR in cell proliferation, MMP-9 in extracellular matrix degradation, and PSMA in prostate cancer cell metabolism [190]. By binding to these genes' products, QDs facilitate the early detection and precise localization of lymph node metastases [191].

Quantum dots offer several advantages over traditional imaging methods such as MRI or CT in detecting lymph node metastasis [192]. Firstly, QDs have higher brightness and photostability, which means they can provide clearer and more durable images [193]. Secondly, their small size allows for better tissue penetration and accumulation in tumor sites [194]. Additionally, the multi-color fluorescence of QDs enables multiplexed imaging to simultaneously track multiple biological processes [195]. For instance, QDs can be designed to target specific tumor markers such as p53, a gene involved in cell cycle regulation, BRCA1/2 associated with DNA repair, KRAS linked to cell signaling, PTEN involved in tumor suppression, and BCL-2 associated with apoptosis [196]. These markers are critical in understanding the biology of metastatic cancer cells in lymph nodes [197]. The precise targeting and imaging of these factors with QDs lead to a more accurate assessment of tumor spread and prognosis [198].

Quantum dots can play a pivotal role in the targeted treatment of lymph node metastasis [199]. By conjugating QDs with therapeutic agents and targeting molecules, they can be directed to specific tumor sites [200]. For instance, genes like TNF-α, involved in inflammatory response, CD20 found on B lymphocytes, CD33 expressed in myeloid cells, EGFR, and HER2 can be targets for these QD-conjugates [201]. The localization of QDs at tumor sites allows for the direct delivery of therapeutics, minimizing systemic side effects [202]. For example, QDs linked to TNF-α can enhance the anti-tumor immune response, while those targeting CD20 or CD33 can be used in targeted therapies for specific types of leukemia or lymphoma [203]. Additionally, the use of QDs in photothermal and photodynamic therapy provides a method for destroying metastatic cells by generating localized heat or reactive oxygen species when irradiated with specific wavelengths of light [204].

Despite their potential, there are several challenges and limitations to the use of quantum dots in lymph node metastasis imaging [204]. Toxicity is a primary concern, as many QDs are made of heavy metals like cadmium, which can be harmful [205, 206]. Biocompatibility and clearance from the body are also major considerations [204]. Furthermore, the potential for non-specific accumulation and the risk of false positives cannot be overlooked [205]. Factors like size, surface charge, and coating of QDs influence their biodistribution and clearance [206]. Genes such as ABC transporters, involved in drug resistance and clearance, CYP enzymes responsible for metabolism, HLA genes linked to immune response, MDR1 associated with drug efflux, and GSTs involved in detoxification play a significant role in how the body interacts with and processes QDs [207]. Understanding these genetic factors is crucial for improving the safety and efficacy of QD-based imaging technologies [208].

Imaging cancer cells in lymph nodes

Imaging techniques are crucial in identifying lymph node metastasis in cancer patients, significantly impacting treatment planning [209]. Techniques like PET, CT, and MRI are commonly used to detect metastatic cancer cells in lymph nodes [210]. For example, PET scans are sensitive in identifying metabolic activity, which is often higher in cancer cells [211]. This helps in pinpointing metastatic sites [212]. Furthermore, imaging aids in staging cancer, which is vital for determining the appropriate treatment plan [213]. For instance, if metastasis is detected in the lymph nodes, it may indicate a need for more aggressive treatment like chemotherapy or radiation [215]. Imaging also helps in monitoring the effectiveness of treatment and in early detection of recurrence [216]. In terms of genes and factors, genes like VEGF (involved in angiogenesis), MMPs (involved in extracellular matrix remodeling), E-cadherin (a cell adhesion molecule), CTCs (Circulating Tumor Cells, which aid in metastasis), and PD-L1 (involved in immune response evasion) play significant roles in metastasis and are potential biomarkers for imaging [217].

Specific genes are known to influence the likelihood and nature of lymph node metastasis in cancer [218]. BRCA1, commonly associated with breast and ovarian cancers, when mutated, leads to DNA repair defects that can cause cancer progression and metastasis [200]. p53, often referred to as the “guardian of the genome”, when mutated, results in uncontrolled cell division, potentially leading to metastasis [201]. Mutations in RAS genes can lead to uncontrolled cell signaling, promoting cancer cell proliferation and metastasis [202]. HER2 is overexpressed in some breast cancers and is associated with aggressive tumor growth and higher rates of metastasis [203]. EGFR, when overexpressed or mutated, contributes to enhanced proliferation, angiogenesis, and reduced apoptosis, facilitating tumor growth and metastasis [204]. Understanding these genes’ roles helps in developing targeted therapies and in prognosticating the course of the disease [204].

Traditional imaging methods may not detect micro-metastases or differentiate between reactive and metastatic lymph nodes effectively [205]. Advancements like functional imaging (using PET-MRI) and the development of specific biomarkers have improved the sensitivity and specificity of detection [206]. Molecular imaging, which targets specific genes or proteins, is an emerging field that offers precise detection of metastatic cells [207]. For instance, imaging agents targeting VEGF can highlight areas of angiogenesis common in tumors [208]. Genes like MMPs, which are involved in tissue remodeling during metastasis, can also be targeted for imaging [209]. Other advancements include the use of nanotechnology and liquid biopsies (CTCs analysis) for early detection and monitoring of metastasis [210].

Environmental and lifestyle factors significantly impact the risk and progression of lymph node metastasis in cancer [211]. Factors such as smoking, alcohol consumption, obesity, and exposure to carcinogens are known to increase the risk of cancer and its metastasis [212]. For instance, tobacco smoke contains carcinogens that can cause mutations in genes like p53 and RAS, leading to cancer progression and metastasis [213]. Obesity is linked to increased levels of insulin and insulin-like growth factors, which can promote tumor growth and metastasis [214]. Dietary factors also play a role; for instance, high-fat diets are associated with increased levels of certain hormones that can promote cancer growth [215]. Regular physical activity and a healthy diet are protective factors that can reduce the risk of cancer and its metastasis [216]. Understanding these environmental and lifestyle factors helps in developing preventive strategies and personalized treatment plans [217]. Environmental and lifestyle factors significantly impact the identification of cancer in lymph nodes. These factors, such as smoking, diet, and exposure to toxins, can influence the likelihood of cancer development and metastasis, affecting lymph node involvement. Understanding these factors helps in early detection and targeted prevention strategies [212].

Personalized medicine, particularly with genetic profiling, holds great promise in the context of lymph node metastasis in cancer [218]. Advances in genomics have enabled detailed profiling of tumors, allowing for more targeted and effective treatments [219]. For example, identifying specific mutations in genes like EGFR or HER2 can guide the use of targeted therapies that are more effective and have fewer side effects [220]. The future of personalized medicine also involves developing new biomarkers for early detection and monitoring of metastasis, as well as for predicting treatment response [221]. Furthermore, ongoing research in gene therapy and immunotherapy is opening new avenues for treating metastatic cancer [222]. Personalized medicine aims to tailor treatment to individual patient profiles, improving outcomes and quality of life for cancer patients [223].

The study establishes that the smallest detectable size of metastatic cancer cells in lymph nodes using advanced imaging techniques is approximately a few micrometers in diameter [220]. This detection limit was determined through rigorous experimental procedures, utilizing high-resolution molecular imaging modalities such as PET, CT, and MRI, capable of identifying cancer cells at this microscopic scale [219]. Detecting cancer cells of this size is crucial for early and accurate staging, as well as for guiding treatment strategies. Further analysis and clarification of the detection parameters have been provided to enhance the precision of these findings, contributing to improved diagnosis and treatment planning for patients with lymph node metastasis [223].

Imaging immune cells and molecular interactions

Immune cells play a crucial role in lymph node metastasis in cancer, acting as a double-edged sword [224]. On one hand, they can suppress tumor growth, while on the other, they may facilitate tumor spread [225]. Imaging techniques such as PET scans, MRI, and advanced microscopy have enabled a deeper understanding of these interactions [226]. For example, T cells (CD8 + and CD4 +), known for their tumor-fighting abilities, can be visualized congregating around tumor cells, indicating an immune response [227]. However, some T cells (like regulatory T cells or Tregs) can suppress immune responses, thereby aiding cancer spread [228]. B cells, another type of immune cell, are often found in tertiary lymphoid structures and can influence tumor behavior [229]. Macrophages (M1 and M2 types) have dual roles; M1 macrophages combat cancer, while M2 macrophages can support tumor growth and metastasis [230]. Natural Killer (NK) cells are critical in early cancer detection and elimination, but their activity can be diminished in a tumor microenvironment [228]. Dendritic cells present antigens to T cells, but can also be altered by tumors to evade immune detection (Fig. 4). Understanding these complex interactions through imaging provides insights into the mechanisms of lymph node metastasis, paving the way for targeted therapies [230].

Fig. 4

illustrates the following processes: a Conventional type 1 dendritic cells (cDC1s) capture and deliver tumor antigens to tumor-draining lymph nodes (TDLNs), where they activate naïve CD8 + T cells, leading to the development of cytotoxic effector CD8 + T cells. This image is copyrighted by the Francis Crick Institute in 2018 [231]. b TDLNs exhibit a high concentration of tumor-specific PD-1 + T cells. Inhibiting PD-L1 in TDLNs results in the formation of progenitor-exhausted T cells, which then infiltrate the tumor, thereby boosting antitumor immunity. This part of the figure is copyrighted by Elsevier Inc. in 2020 [232]. Definitions included in this description are cDC1 for conventional type 1 dendritic cells, and TDLN for tumor-draining lymph node

Molecular interactions within lymph nodes play a pivotal role in cancer metastasis [232]. Advanced imaging techniques like fluorescence microscopy and confocal microscopy have shed light on these interactions [233]. Key molecules include cytokines, chemokines, adhesion molecules, and growth factors [234]. Cytokines like Interleukin-6 (IL-6) and Tumor Necrosis Factor-alpha (TNF-α) can promote tumor growth and metastasis [235]. Chemokines such as CCL21 and CXCL12 guide immune cells and cancer cells to lymph nodes, influencing metastasis [236]. Adhesion molecules like ICAM-1 and VCAM-1 facilitate the binding of cancer cells to the lymph node endothelium [237]. Growth factors such as VEGF and TGF-β play roles in angiogenesis and immune suppression, respectively [238]. These molecular interactions, visualized through imaging, highlight the dynamic environment of lymph nodes and their influence on cancer progression [239].

Immune checkpoint molecules, such as PD-1, PD-L1, CTLA-4, LAG-3, and TIM-3, play significant roles in regulating immune responses in cancer, including lymph node metastasis [240]. These molecules, visualized through techniques like immunohistochemistry and PET scans, are often upregulated in cancer cells and immune cells within the tumor microenvironment [241]. PD-1 and PD-L1 interaction, for instance, can inhibit T cell activity, allowing cancer cells to evade immune surveillance [242]. CTLA-4 competes with CD28 for binding to B7 molecules on antigen-presenting cells, reducing T cell activation [243]. LAG-3 and TIM-3 are other inhibitory receptors that contribute to T cell exhaustion [227]. By imaging these interactions, researchers understand how tumors exploit immune checkpoints to promote metastasis and escape immune destruction [244]. This knowledge has led to the development of checkpoint inhibitors as a form of cancer therapy [245].

Lymphangiogenesis, the formation of new lymphatic vessels, is a critical process in lymph node metastasis in cancer [6, 246]. Imaging techniques like lymphoscintigraphy, MRI, and near-infrared fluorescence imaging have been instrumental in studying this phenomenon [247]. Factors such as VEGF-C, VEGF-D, and their receptor VEGFR-3 are heavily involved in promoting lymphangiogenesis [248]. These factors, visualized through various imaging modalities, lead to the expansion of the lymphatic network, facilitating the spread of cancer cells to lymph nodes [249]. Angiopoietins (Ang-1 and Ang-2) and their receptor Tie-2 also play roles in lymphatic vessel remodeling and stability [250]. Prox1, a transcription factor, is essential for the differentiation and maintenance of lymphatic endothelial cells [251]. Through imaging, the process of lymphangiogenesis and its contribution to cancer metastasis can be observed, offering insights into potential therapeutic targets [252].

Role of photothermal therapy (PTT) and photodynamic therapy (PDT) in the treatment of lymph node metastasis

Recent advances in the treatment of lymph node metastases have highlighted the potential of Photothermal Therapy (PTT) and Photodynamic Therapy (PDT) as effective strategies in the oncological arsenal. These modalities offer minimally invasive options aimed at targeted destruction of cancer cells with minimal damage to surrounding healthy tissues, which is particularly crucial in the management of lymph node metastases [252]. PTT involves the use of nanoparticles that are excited by near-infrared light, leading to the generation of heat that selectively destroys cancerous cells [161]. The application of PTT in lymph node metastasis is predicated on the ability of these nanoparticles to specifically accumulate in metastatic lymph nodes due to enhanced permeability and retention effect. Studies have shown that PTT can effectively eradicate lymphatic tumors and prevent further spread of the disease. The precise control over the area being treated with PTT minimizes the risk to adjacent structures and preserves lymphatic function, which is essential for preventing complications such as lymphedema [233]. PDT is another promising approach where photosensitizing agents are administered that selectively accumulate in cancerous tissues. Upon activation by a specific wavelength of light, these agents produce reactive oxygen species that induce cell death. PDT has been particularly noted for its dual role in directly killing tumor cells and damaging the vasculature supplying the tumor, thereby causing tumor necrosis and reducing metastatic potential. The specificity of light activation in PDT allows for targeted therapy, which is crucial for lymph node metastases that are adjacent to critical anatomical structures [204]. PTT and PDT leverage the enhanced permeability and retention effect, which allows nanoparticles and photosensitizing agents to accumulate more readily in tumor tissues than in normal tissues [154]. This selective accumulation enables targeted treatment of metastatic lymph nodes, minimizing damage to surrounding healthy structures and reducing systemic side effects. The primary benefits include their minimally invasive nature and their ability to precisely target affected lymph nodes. PTT uses heat generated by nanoparticles to destroy cancer cells, while PDT uses light-activated photosensitizers to initiate a chemical reaction that kills cancer cells and disrupts tumor vasculature. Both methods offer controlled treatment, preserving lymphatic architecture and function, which is crucial for preventing secondary complications like lymphedema [252].

Rationale for targeted therapy in lymph node metastasis

Drugs targeting the HER2/neu receptor, such as Trastuzumab, work by binding to the HER2 protein on the surface of cancer cells [253]. This binding inhibits the proliferation of cancer cells that overexpress this receptor, which is a common feature in some breast cancers [254]. For example, Trastuzumab, a monoclonal antibody, binds to the HER2/neu receptor, blocking its ability to receive growth signals, thus inhibiting tumor growth [255]. Besides HER2/neu, other genes play significant roles in breast cancer [256]. One such gene is BRCA1/BRCA2, mutations in which increase the risk of breast cancer and are targets for PARP inhibitors [257]. The TP53 gene, often mutated in breast cancer, is crucial for DNA repair and apoptosis [258]. The PIK3CA gene, frequently mutated in breast cancer, is involved in cell growth and survival pathways [259]. Estrogen receptor (ER) and progesterone receptor (PR) genes influence the growth of breast cancer cells through hormone signaling pathways [260]. Understanding these genes’ roles and functions provides a basis for targeted therapeutic interventions, offering more personalized and effective treatment options for breast cancer patients [261].

PARP inhibitors, such as Olaparib, target and inhibit the enzyme Poly (ADP-ribose) polymerase (PARP), which plays a critical role in repairing DNA single-strand breaks [262]. In cells with BRCA1 or BRCA2 mutations, the double-strand DNA repair mechanism is already compromised [263]. When PARP inhibitors are used, they exploit this vulnerability by blocking the single-strand DNA repair pathway, leading to cell death, particularly in cancer cells [264]. Besides BRCA1 and BRCA2, other genes involved in the DNA repair pathway include ATM, which senses DNA damage and initiates repair; CHEK2, which works in concert with ATM to regulate cell cycle and repair; PALB2, which assists BRCA2 in repairing double-strand breaks; and RAD51, which plays a key role in homologous recombination repair [265]. Understanding these genes’ roles in DNA repair pathways has been crucial in developing targeted therapies like PARP inhibitors, which offer a more tailored approach in treating cancers, particularly those with BRCA mutations [266].

Tyrosine kinase inhibitors (TKIs), such as Imatinib, target tyrosine kinases, enzymes that play a vital role in the signaling pathways that control cell growth and survival [267]. By inhibiting these enzymes, TKIs can block the proliferation of cancer cells [268]. Imatinib, for instance, is effective against chronic myeloid leukemia (CML) by targeting the BCR-ABL fusion protein, a specific type of tyrosine kinase [269]. Other genes crucial for cancer cell growth and survival include EGFR, which encodes a protein involved in cell growth and division; KRAS, which plays a role in cell signaling pathways that control cell growth and death; BCL-2, which helps regulate cell death (apoptosis); MYC, which is involved in cell cycle progression and apoptosis; and PTEN, a tumor suppressor gene that negatively regulates the PI3K/AKT signaling pathway [270]. Understanding the functions of these genes has led to the development of targeted therapies that can effectively combat cancer by disrupting specific molecular pathways crucial for tumor growth and survival [271].

PD-1/PD-L1 inhibitors, such as Nivolumab and Pembrolizumab, enhance the immune system’s ability to fight cancer by blocking the interaction between PD-1 receptors on T-cells and PD-L1 proteins on cancer cells [272]. Normally, this interaction helps to keep the immune system in check, but cancer cells can exploit it to avoid immune attack [273]. By inhibiting this interaction, PD-1/PD-L1 inhibitors unmask cancer cells, allowing the immune system to recognize and destroy them [274]. Other significant immune checkpoints include CTLA-4, another receptor on T-cells that, when blocked, can enhance immune responses against cancer cells; LAG-3, which negatively regulates T-cell proliferation; TIM-3, which is involved in immune tolerance and is often upregulated in advanced cancers; and TIGIT, which also functions as an immune checkpoint and is a target for cancer immunotherapy [275]. Research into these checkpoints has revolutionized cancer treatment, offering new strategies to harness the immune system against cancer [276].

Angiogenesis inhibitors, such as Bevacizumab, which targets vascular endothelial growth factor (VEGF), play a crucial role in cancer treatment by disrupting the tumor's blood supply [277]. Tumors need blood vessels to provide oxygen and nutrients for their growth and to remove waste products [209]. By inhibiting angiogenesis, these drugs starve the tumor of its necessary supplies, hindering its growth and spread [278]. Other genes involved in tumor blood supply include FGF (Fibroblast Growth Factor), which also stimulates blood vessel formation; PDGF (Platelet-Derived Growth Factor), which is involved in the growth of blood vessels and is a target for some cancer treatments; TGF-β (Transforming Growth Factor Beta), which plays a role in angiogenesis and tumor progression; and HIF-1 (Hypoxia-Inducible Factor 1), a transcription factor that responds to low oxygen levels and can promote angiogenesis [279]. Understanding these genes and their roles in angiogenesis has been pivotal in developing treatments that can effectively cut off the blood supply to tumors, thereby inhibiting their growth and metastasis [280].

Nanobiotechnological approaches in drug delivery

Table 4 provides an overview of the various nanobiotechnological approaches used in targeted drug delivery for treating lymph node metastasis in different types of cancer. In the realm of nanobiotechnology, several nanoparticles are instrumental in targeting lymph node metastasis in cancer. These include liposomes, dendrimers, quantum dots, solid lipid nanoparticles, and polymeric nanoparticles [281]. Figure 5 illustrates a precision medicine nanoplatform designed for metastatic lymph nodes, facilitating dual-modal imaging using ultrasound and photoacoustic methods. Recent clinical trials have been focusing on various gene delivery methods for treating melanoma. One such experimental treatment is Allovectin-7®, currently in a Phase II trial (NCT00044356). This study aims to determine if Allovectin-7® can effectively reduce the size of melanoma tumors and delay the disease’s progression. Another notable trial involves the use of F5 TCR with dendritic cells, under Phase II (NCT00910650). This trial uses an apheresis product to generate gene-modified MART-1 TCR CTLs and dendritic cells, verifying their expression of the correct TCR. Additionally, a Phase I trial (NCT00512889) is investigating CTLs combined with artificial antigen presenting cells (aAPCs). The focus here is on the feasibility and side effects of administering intravenous infusions of lab-produced CTLs, which are derived from leukapheresis and augmented with additional genes. GVAX is being examined in a Phase I trial (NCT00258687) for its efficacy against Clear Cell Sarcoma. The specific details and outcomes of this trial are encapsulated under the identifier Procedia#apol14p. The trial for HBI 0201 /ESO TCRT, a Phase I/II study (NCT05296564), is investigating the use of anti-NY-ESO-1 TCR-Gene Engineered Lymphocytes (HBI 0201-ESO TCRT) by infusion in patients with NY-ESO-1 expressing metastatic cancers. This trial aims to evaluate the dose escalation, safety, and efficacy of this approach. In a similar vein, HX008/OH2 is in a Phase I/II trial (NCT04616443). This study involves the use of the herpes simplex virus type 2 strain HG52, genetically modified to become OH2, an oncolytic virus replicating only in tumor cells. This virus is enhanced with a gene encoding human granulocyte macrophage colony-stimulating factor (GM-CSF), potentially inducing a stronger antitumor immune response. Finally, the RNA/Lipo-MERIT vaccine, in a Phase I trial, targets four specific malignant melanoma-associated antigens: Tyrosinase, Melanoma-Associated Antigen A3 (MAGE-A3), New York-ESO 1 (NY-ESO-1), and Trans-membrane phosphatase with Tensin Homology (TPTE). The goal of this study is to assess the vaccine's efficacy against these targets in melanoma treatment. Each of these nanoparticles plays a crucial role in improving the accuracy and effectiveness of cancer treatments, highlighting the innovative advancements in nanobiotechnology (Fig. 6).

Table 4 Nanobiotechnological advances in targeted drug delivery for lymph node metastasis in cancer

Fig. 5

illustrates a precision medicine platform designed for visualizing metastatic lymph nodes. This platform employs ultrasonic/photoacoustic dual-modal imaging to guide targeted hyperthermia and combined chemotherapy directly at the site. The image, copyrighted in 2021 by Springer Nature [282], features several components: nanoparticles (NP), perfluorohexane (PFH), poly(lactic-co-glycolic acid) (PLGA), and lymph nodes (LN)

Fig. 6

Copyright 2013 by the European Association of Urology [283]. b The implementation of a near-infrared (NIR) probe for detecting lymph node metastasis (LNM) in mice. The images show NIR imaging-assisted sentinel lymph node (SLN) surgery in a mouse model of orthotopic 4T1 breast cancer. Copyright 2020 by Wiley–VCH [284]

Two different applications: a The use of ultrasmall superparamagnetic iron oxide (USPIO) nanoparticles for identifying metastases in normally-sized pelvic LN in individuals with bladder and prostate cancer. These nanoparticles are absorbed by macrophages, resulting in a reduced signal in T2- or T2*-weighted magnetic resonance imaging (MRI). This reduction is not observed in malignant LN (indicated by an arrow) due to their lower macrophage count and minimal absorption of USPIO nanoparticles, unlike benign LN (marked by an arrowhead).

Liposomes are a pivotal component in the treatment of lymph node metastasis in cancer, primarily due to their unique structural and compositional characteristics [283]. As spherical vesicles formed from lipid bilayers, they encapsulate chemotherapeutic drugs, protecting them from degradation and ensuring targeted delivery [284]. Once administered, liposomes circulate in the bloodstream and accumulate in the cancer-affected lymph nodes [285]. Their design allows them to release the encapsulated drugs specifically at the metastatic site [286]. This targeted release ensures a higher concentration of the drug at the tumor site, enhancing therapeutic efficacy [287]. Moreover, liposomes can be engineered to be sensitive to the microenvironment of cancer cells, such as pH or temperature, triggering drug release precisely where needed [288]. This not only maximizes the impact on cancer cells but also significantly reduces the systemic toxicity often associated with chemotherapy [289]. The use of liposomes in targeting lymph node metastasis exemplifies the progress in personalized medicine, offering a more effective and safer alternative to conventional cancer treatments [290].

Dendrimers are a novel class of nanoparticles playing a transformative role in targeting lymph node metastasis in cancer treatments [291]. These nanosized, branched polymers have a unique architecture that allows for the attachment of multiple drug molecules [292]. The multivalency of dendrimers enables the simultaneous delivery of different therapeutic agents, potentially enhancing treatment efficacy [293]. Their size and surface functionality can be precisely controlled, allowing for targeted delivery to metastatic sites in the lymph nodes [294]. Dendrimers can be engineered to interact with specific cancer cell markers, ensuring that the drug payload is delivered directly to cancer cells, thereby reducing the impact on healthy cells [295]. Furthermore, the branched structure of dendrimers provides a controlled release mechanism, ensuring that the drugs are released over a sustained period, which can be crucial for effective cancer treatment [296]. This controlled release also reduces the frequency of drug administration, improving patient compliance and comfort [297]. Dendrimers' versatility and efficiency in drug delivery systems represent a significant advancement in nanotechnology-based cancer therapies, providing a promising approach to treating lymph node metastasis [298].

Quantum dots (QDs) are semiconductor nanoparticles that offer groundbreaking applications in the management of lymph node metastasis in cancer [299]. Their primary role lies in imaging and tracking the spread of cancer to the lymph nodes [300]. Quantum dots have unique optical properties, such as size-tunable light emission, which makes them highly effective for biomedical imaging [301]. When used in cancer patients, QDs can be engineered to bind to specific tumor markers, allowing for precise visualization of metastatic cancer cells in the lymph nodes [302]. This targeted imaging provides invaluable information about the extent and progression of cancer, aiding in the formulation of effective treatment strategies [303]. Additionally, the high brightness and stability of QDs enhance the quality of imaging, facilitating early detection of metastasis, which is crucial for successful cancer treatment [304]. The real-time tracking capability of quantum dots also allows for monitoring the efficacy of therapeutic interventions, enabling adjustments in treatment plans as needed [305]. The integration of quantum dots into cancer management underscores the potential of nanotechnology in advancing diagnostic and therapeutic approaches in oncology [306].

Solid lipid nanoparticles (SLNs) and polymeric nanoparticles are critical in cancer treatment, particularly for targeting lymph node metastasis [307]. SLNs are characterized by their solid lipid core, which can effectively encapsulate lipophilic drugs, enhancing their solubility and stability [308]. This feature is particularly beneficial in the treatment of cancer, where many chemotherapeutic agents are hydrophobic [309]. The biodegradable nature of SLNs ensures minimal toxicity, and their ability to bypass biological barriers allows for efficient drug delivery to lymph nodes [310]. On the other hand, polymeric nanoparticles offer versatility in terms of composition, structure, and functionality [311]. They can be engineered to have specific shapes, sizes, and surface characteristics, enabling targeted drug delivery [312]. Polymers can be functionalized with ligands that bind specifically to cancer cells, ensuring that the drug payload is delivered directly to the affected lymph nodes [313]. Both SLNs and polymeric nanoparticles can be designed to release their drug payload in a controlled manner, providing a sustained therapeutic effect [314]. This controlled release reduces the need for frequent dosing, improving patient compliance [315]. The use of SLNs and polymeric nanoparticles in targeting lymph node metastasis represents a significant advancement in nanotechnology-based drug delivery systems, offering a more effective and patient-friendly approach to cancer treatment [316]. Figure 7 depicts recent advancements in gene delivery for melanoma using polymeric and lipid-based nanocarriers.

Fig. 7

Recent advancements in polymer and lipid-based nanocarriers for gene therapy in melanoma. This includes A, i a diagram of RRPHC ternary complexes, (ii) a comparison of transfection efficiency in B16F10 cells using PF33/pGFP, RRPHC/pGFP, and Lipofectamine 2000/pGFP, and (iii) the administration of HAC/pDNA and RRPHC/pDNA through intravenous injection, followed by in vivo and ex vivo fluorescence imaging in A375 tumor-bearing nude mice (specifically RRPHC). This information, originally from L. Li et al., 2016, is used with Elsevier's permission [317]. Section (B) focuses on human skin samples that were intradermally injected with lipid nanoparticle (LNP) formulations varying in lipid composition and dosage. This part includes (i) ex vivo imaging of the samples after 11 days and (ii) quantification of the luciferase image. This section is reproduced with permission from Blakney et al., 2019, and is under the copyright of the American Chemical Society [318]

Nanobiotechnology in enhancing immunotherapy

Nanoparticles play a crucial role in enhancing the efficacy of immunotherapy for treating lymph node metastases in cancer [376]. Their small size and customizable surface properties allow them to target and accumulate in lymph nodes effectively [377]. This targeted delivery is vital in improving the immunotherapy response [378]. For instance, liposomal nanoparticles can deliver PD-1 inhibitors directly to lymph nodes, significantly enhancing T-cell activation against cancer cells [379]. PD-1, or Programmed Death-1, is a crucial gene in regulating the immune system's response to cancer cells [380]. Inhibiting PD-1 allows T-cells to attack cancer cells more effectively [381]. Similarly, nanoparticles carrying CTLA-4 antibodies can inhibit the CTLA-4 pathway, promoting an immune response against tumor cells [382]. CTLA-4, or Cytotoxic T-Lymphocyte-Associated protein 4, is another immune checkpoint that, when blocked, can enhance the immune system's ability to fight cancer [383]. Additionally, the delivery of siRNA targeting genes like TGF-β, which plays a role in immune suppression in the tumor microenvironment, can further enhance the immune response [384]. TGF-β, or Transforming Growth Factor Beta, is often involved in creating an environment that suppresses the immune system's ability to combat cancer [385]. Moreover, nanoparticles can modulate the tumor microenvironment by altering the expression of factors like VEGF and IL-10 [336]. VEGF, or Vascular Endothelial Growth Factor, promotes tumor growth and angiogenesis, while IL-10, or Interleukin-10, is known to suppress immune responses [337]. By targeting these factors, nanoparticles create a more favorable environment for immunotherapy [338]. Lastly, nanoparticles delivering CRISPR/Cas9 gene-editing tools targeting genes like FOXP3 can reduce immune suppression [339]. FOXP3 is often overexpressed in regulatory T cells in cancer and plays a significant role in suppressing the immune response [340]. By editing this gene, nanoparticles can enhance the effectiveness of immunotherapy in treating lymph node metastases in cancer [341].

In the context of cancer immunotherapy, specific genes and factors like PD-1, CTLA-4, TGF-β, VEGF, and IL-10 play pivotal roles, and nanoparticles are engineered to target these effectively [342]. PD-1, or Programmed Death-1, is a gene that codes for a protein on the surface of T-cells [343]. It negatively regulates the immune response, and cancer cells often exploit this pathway to evade immune detection [344]. Nanoparticles can deliver PD-1 inhibitors to lymph nodes, thereby blocking this pathway and enhancing the T-cell-mediated attack on cancer cells [345]. CTLA-4, or Cytotoxic T-Lymphocyte-Associated protein 4, is another checkpoint protein that inhibits T-cell activation [346]. Nanoparticles carrying CTLA-4 antibodies can effectively block this pathway, promoting a stronger immune response against tumor cells [347]. TGF-β, or Transforming Growth Factor Beta, is a multifunctional cytokine that plays a role in immune suppression within the tumor microenvironment [348]. Nanoparticles delivering siRNA to silence TGF-β can prevent this suppression, thereby enhancing the immune system's ability to fight cancer [349]. VEGF, or Vascular Endothelial Growth Factor, is crucial in tumor growth and angiogenesis [350]. Nanoparticles can be designed to modulate VEGF expression, thereby hindering tumor growth and metastasis [351]. Lastly, IL-10, or Interleukin-10, is an anti-inflammatory cytokine that can suppress immune responses in the tumor microenvironment [352]. By targeting IL-10, nanoparticles can shift the balance towards a pro-inflammatory and anti-tumor environment, facilitating more effective immunotherapy [353]. Nanoparticles significantly contribute to the modulation of the tumor microenvironment by targeting factors like VEGF and IL-10 [354]. VEGF, or Vascular Endothelial Growth Factor, is a key protein that stimulates angiogenesis, the formation of new blood vessels, which is essential for tumor growth and metastasis. Nanoparticles can be engineered to interfere with the VEGF pathway, either by delivering agents that inhibit VEGF expression or by silencing the VEGF gene directly [355]. This intervention can effectively starve the tumor of the necessary blood supply, impeding its growth and spread [356].

IL-10, or Interleukin-10, is an anti-inflammatory cytokine that plays a role in suppressing immune responses in the tumor microenvironment [357]. This suppression is beneficial for the tumor, as it allows cancer cells to evade immune detection and destruction [358]. By targeting IL-10 with nanoparticles, either through the delivery of inhibitory molecules or gene silencing techniques, the tumor microenvironment can be shifted towards a more pro-inflammatory state [359]. This change enhances the effectiveness of immune cells against the tumor, thereby improving the overall response of immunotherapy [360]. The modulation of these factors by nanoparticles creates a more favorable environment for the immune system to attack the tumor [361]. By altering the balance of pro- and anti-tumor factors in the tumor microenvironment, nanoparticles help in orchestrating a more potent and targeted attack against cancer cells, leading to improved outcomes in cancer treatment [362]. The delivery of CRISPR/Cas9 gene-editing tools via nanoparticles is a significant advancement in cancer immunotherapy, particularly in targeting genes like FOXP3 [363]. FOXP3, a gene critical in the regulation of regulatory T cells (Tregs), often gets overexpressed in the cancer setting, leading to an increase in Tregs within the tumor microenvironment [356]. These Tregs play a role in suppressing the immune response against cancer cells [364]. By targeting FOXP3, it’s possible to reduce this suppression, enhancing the immune system's capacity to fight cancer [365]. Nanoparticles offer a precise and efficient means to deliver CRISPR/Cas9 to the tumor site [366]. This gene-editing technology can be used to either knock out or modulate the expression of FOXP3 in Tregs [367]. The ability to directly edit genes within the tumor microenvironment is a groundbreaking approach in cancer treatment, as it allows for a more targeted and effective modification of the immune response [368]. Moreover, the use of nanoparticles ensures that the CRISPR/Cas9 system is delivered specifically to the tumor site, minimizing off-target effects and potential systemic side effects [369]. This localized delivery is crucial in maximizing the therapeutic benefits while reducing the risk of unwanted immune reactions or other complications [370]. The integration of CRISPR/Cas9 gene-editing into nanoparticles represents a novel and promising strategy in the fight against cancer, offering a more precise and potentially powerful tool in cancer immunotherapy [371].

Nanoparticles carrying small interfering RNA (siRNA) targeting genes like TGF-β play a critical role in enhancing the immune system's ability to fight cancer [372]. TGF-β, or Transforming Growth Factor Beta, is a cytokine that is often implicated in promoting immune suppression within the tumor microenvironment [373]. It aids in the progression of cancer by inhibiting the immune system's ability to recognize and destroy cancer cells [374]. By using nanoparticles to deliver siRNA specifically designed to silence the TGF-β gene, it's possible to disrupt this immune suppression [375]. The siRNA works by binding to the mRNA of TGF-β, leading to its degradation and preventing the translation of the TGF-β protein [376]. This reduction in TGF-β levels can alleviate the immune-suppressive conditions in the tumor microenvironment, thereby reactivating the immune system's natural ability to fight cancer [377]. The targeted delivery of siRNA via nanoparticles ensures that the interference with TGF-β occurs directly at the tumor site, maximizing the therapeutic impact while minimizing potential side effects elsewhere in the body [378]. This precision not only increases the efficacy of the treatment but also reduces the risk of systemic immune reactions that could occur with broader immune system activation [379].

Integration of imaging and therapeutics

In the realm of theranostic interventions for lymph node metastasis, several innovative approaches have been employed to enhance both the detection and treatment of cancer [296]. Key theranostic interventions include the use of nanoparticles conjugated with therapeutic agents, which are engineered to target metastatic lymph nodes specifically [306]. These nanoparticles not only deliver drugs directly to the cancer cells but also possess imaging capabilities, allowing for simultaneous tracking and treatment of metastases [296]. Additionally, immunotherapeutic strategies targeting lymph node metastases have been combined with molecular imaging techniques to monitor immune responses in real-time [209].

The imaging methods used in these integrated approaches are varied and advanced [358]. Positron Emission Tomography (PET) and MRI are prominent modalities that provide high-resolution images and functional information about lymph node status. PET imaging, often using radiolabeled tracers, facilitates the detection of metabolic activity associated with cancer cells, while MRI offers detailed anatomical visualization [107]. Optical imaging techniques, such as fluorescence and bioluminescence imaging, are also utilized for their ability to provide real-time visualization of therapeutic agent distribution and tumor response. These imaging methods, when combined with targeted therapeutics, offer a powerful toolkit for the precise and effective management of lymph node metastasis in cancer [304].

HER2, or Human Epidermal Growth Factor Receptor 2, plays a crucial role in the progression of certain breast cancers [380]. This gene, when overexpressed, leads to aggressive cancer growth and spread, including to lymph nodes [381]. In theranostics, the overexpression of HER2 becomes a target for specialized agents that combine diagnostic imaging and therapeutic intervention [382]. By targeting HER2, theranostic agents can accurately localize metastatic sites in lymph nodes and deliver targeted treatment directly to these areas [383]. This approach is particularly effective because it enables personalized therapy, ensuring that patients with HER2-positive breast cancer receive treatments specifically tailored to their genetic profile [384]. Additionally, by focusing on the unique genetic makeup of the cancer cells, theranostic approaches reduce the impact on healthy tissues, minimizing side effects and enhancing treatment efficacy [385].

The CD20 gene, present on the surface of B cells, is instrumental in the theranostic approach to treating lymphomas, particularly those that metastasize to lymph nodes [386]. Targeting CD20 allows for the precise localization and treatment of these lymphomas [387]. Theranostic agents designed to bind to CD20 can be used both for diagnostic imaging and for delivering targeted therapies directly to cancer cells [388]. This targeted approach ensures that therapeutic agents are concentrated at the site of the tumor, maximizing their effectiveness while minimizing damage to healthy cells [388]. In the context of lymph node metastasis, this precise targeting is vital, as it allows for the treatment of cancer cells that have spread beyond the primary tumor site, offering a more comprehensive approach to cancer therapy [389].

Prostate-Specific Membrane Antigen (PSMA) is highly significant in the field of prostate cancer theranostics, particularly for identifying and treating metastatic sites in lymph nodes [390]. PSMA is a protein commonly found on prostate cancer cells, including those that have metastasized to lymph nodes [391]. In theranostic applications, agents targeting PSMA are used both for diagnostic imaging and for delivering targeted therapeutic drugs [392]. This dual functionality allows for the precise visualization of metastatic sites, enabling clinicians to better understand the extent and specific locations of the cancer spread [393]. Subsequently, the same PSMA-targeting agents can deliver treatment directly to these identified sites, ensuring a focused and effective therapeutic response [296]. This approach is particularly valuable in managing metastatic prostate cancer, as it allows for personalized treatment plans based on the specific characteristics of the patient's cancer [394].

KRAS gene mutations are common in various cancers and play a pivotal role in influencing personalized therapy in cancer theranostics, especially concerning lymph node metastasis [395]. These mutations often lead to uncontrolled cell growth and cancer progression [396]. In theranostics, detecting KRAS mutations is essential for developing personalized treatment strategies [397]. Theranostic agents can be tailored to target these specific mutations, allowing for precise treatment of cancers that have spread to lymph nodes [397]. By focusing on the unique genetic alterations of the cancer cells, theranostic approaches enable the delivery of highly specific and effective treatments, thereby improving the overall prognosis [397]. This personalized approach is particularly beneficial in treating cancers with KRAS mutations, as it addresses the genetic basis of the disease, leading to more effective and targeted therapy [398].

The CA125 gene, a marker for ovarian cancer, is crucial in the theranostic approach to treating this disease, especially when it involves lymph node metastasis [399]. In ovarian cancer, the CA125 protein is often overexpressed and can be used as a biomarker for the presence and progression of the disease [399]. In theranostics, agents that target the CA125 gene are employed both for diagnostic imaging and for the targeted delivery of therapeutics [400]. This dual application is particularly beneficial for identifying and treating metastatic sites in lymph nodes [401]. By specifically targeting the CA125 marker, theranostic agents can accurately locate metastatic cancer cells and deliver effective treatment directly to these sites [402]. This targeted approach not only enhances the effectiveness of the treatment but also reduces the likelihood of damaging healthy tissues, thereby improving the safety and outcomes for patients with ovarian cancer [403].

Differentiating sentinel lymph nodes from regional lymph nodes in cancer management

The identification of sentinel lymph nodes versus regional lymph nodes is a pivotal component in the staging and treatment of cancer, particularly in malignancies such as breast cancer and melanoma [376]. Sentinel lymph nodes are the first lymph nodes to which cancer cells are most likely to spread from a primary tumor. This concept is based on the premise that lymphatic drainage from a tumor follows a predictable pathway, initially involving one or a few key nodes before disseminating to a broader regional network [350].

The process of detecting SLNs typically involves injecting a tracer substance, such as a radioactive isotope or a blue dye, near the tumor site. This tracer travels through the lymphatic system and accumulates in the sentinel nodes [317]. Surgeons then use a gamma probe to detect the radioactive signal or visually identify the blue-stained nodes. This targeted approach allows for the removal of only the sentinel nodes for pathological examination, significantly reducing the need for extensive lymph node dissection and its associated morbidities [308].

In contrast, regional lymph nodes encompass a wider array of nodes within the lymphatic drainage basin of the tumor [393]. Assessing regional lymph nodes often involves more comprehensive procedures, such as axillary lymph node dissection (ALND) in breast cancer or inguinal lymph node dissection in melanoma. These procedures aim to remove a larger number of lymph nodes to evaluate the extent of cancer spread. While this provides thorough staging information and helps in planning further treatment, it also carries a higher risk of complications, including lymphedema, infection, and nerve damage [397].

The distinction between SLNs and regional lymph nodes is crucial for personalized cancer treatment. SLN biopsy is less invasive and focuses on the nodes most likely to harbor metastasis, allowing for early detection and timely intervention with minimal impact on the patient's quality of life [381]. If the sentinel nodes are free of cancer, patients can often avoid more extensive lymph node surgery. Conversely, if metastasis is detected in the SLNs, it may necessitate further regional lymph node assessment and more aggressive treatment strategies [384].

Advancements in imaging technologies, such as single-photon emission computed tomography (SPECT) combined with CT (SPECT/CT), have further refined the identification and localization of sentinel lymph nodes [388]. These imaging modalities provide three-dimensional visualization of the tracer uptake, enhancing the accuracy of sentinel lymph node detection and facilitating more precise surgical planning [390].

Clinical trials

The research field of oncology is advancing with multiple clinical trials focusing on the diagnosis and treatment of lymph node metastases across various types of cancer. These trials utilize different models, approaches, and technologies, aiming to improve patient outcomes through more accurate diagnosis and effective treatment plans.

One such trial is the “Prediction Model for Lateral Lymph Node Metastasis” under study ID NCT04635488, which is currently of unknown status. This observational study focuses on rectal cancer, examining the metastasis rate of lateral lymph nodes through a prospective cohort model. The primary procedure involved is lateral lymph node dissection, seeking to observe and potentially predict lymph node involvement.

Similarly, the study "Distribution of Lymph Node Metastases in Esophageal Carcinoma" (NCT03222895) is actively recruiting participants. It aims to map the spread of lymph node metastases in esophageal cancer, testing the accuracy of preoperative diagnostics, and understanding the prognostic value of various lymph node stations. This observational cohort study also adopts a prospective approach, reflecting a growing trend in exploring the spatial distribution of metastatic nodes.

For pancreatic cancer, the "Para-aortic Lymph Node Metastasis in Resectable Pancreatic Cancer" trial (NCT06065891) is recruiting to investigate the prevalence and prognostic significance of para-aortic lymph node involvement. This interventional study involves PALN resection to determine its impact on patient prognosis after curative resection, underpinning the direct intervention approach in surgical oncology research.

Another notable trial, "Selective Lymph Node Dissection Using Fluorescent Dye in Node-positive Breast Cancer" (NCT02781259), though currently of unknown status, employs both a drug (Indocyanine green) and imaging devices to improve the precision of axillary lymph node dissection. This Phase 4, diagnostic-focused trial explores clinicopathological factors associated with lymph node metastasis, illustrating the integration of advanced imaging and pharmacological tools in surgical procedures.

In contrast, the "Detecting Lymph Node Metastasis in Intrahepatic Cholangiocarcinoma" study (NCT06381648), also known as LyMIC, represents an observational, retrospective case–control model aiming to enhance diagnostic accuracy by measuring sensitivity, specificity, and overall accuracy of lymph node metastasis detection in cholangiocarcinoma.

Challenges and future perspectives

NPs and nanoconjugates have shown great promise in the diagnosis and treatment of lymph node metastasis, but they are not without limitations [139]. One key limitation is the difficulty in effectively targeting and delivering NPs/nanoconjugates to lymph nodes. Lymph nodes have a complex microenvironment with various physical and biological barriers that can hinder the accumulation and penetration of NPs [130]. The size, shape, and surface properties of NPs need to be carefully engineered to optimize lymph node targeting, which can be challenging. Additionally, the heterogeneity of lymph node metastases, in terms of their location, size, and degree of metastatic infiltration, makes it difficult to develop a one-size-fits-all NP/nanoconjugate solution [110].

Another limitation is the potential for off-target effects and toxicity. NPs, especially those made of inorganic materials, can potentially accumulate in non-target organs and induce unwanted side effects [45]. This is a concern not only for diagnostic imaging but also for therapeutic applications where NPs/nanoconjugates may be used to deliver cytotoxic drugs or to induce local immune responses. Careful evaluation of the pharmacokinetics, biodistribution, and safety profile of NPs/nanoconjugates is crucial before clinical translation. Despite these limitations, ongoing research continues to address these challenges, with the ultimate goal of developing more effective and safer NP-based strategies for the management of lymph node metastasis [112].

Molecular imaging faces several challenges in accurately detecting lymph node metastasis in cancer [396]. Firstly, sensitivity and specificity remain a primary concern [404]. Traditional imaging techniques may miss micro-metastases, which are crucial for early detection and treatment [405]. Innovations in molecular imaging strive to enhance the detection of these small metastatic sites [406]. For example, the use of novel biomarkers or tracers that target specific cancer cell properties can improve sensitivity [397]. Secondly, there's a challenge in distinguishing between reactive lymph nodes and those with metastatic disease [398]. This differentiation is vital for accurate staging and treatment planning [399]. Thirdly, the integration of molecular imaging data with other diagnostic modalities, like histopathology, enhances the overall diagnostic accuracy but requires sophisticated data analysis techniques [400]. Fourthly, patient safety and comfort are always a priority, necessitating the development of non-invasive and minimally invasive techniques [401]. Finally, the high cost and accessibility of advanced molecular imaging technologies limit their widespread use, especially in resource-limited settings [402]. Addressing these challenges will require continued research and development in molecular imaging technologies, biomarker discovery, and data integration methods [404]. Table 5 highlights the main aspects of the topic, outlines the current challenges faced in each area, and presents the anticipated future developments or perspectives.

Table 5 Challenges and future perspectives in molecular imaging and targeted therapeutics for lymph node metastasis in cancer

Targeted therapeutics have significantly advanced the treatment of lymph node metastasis in cancer, offering more personalized and effective approaches (Fig. 8). First, the development of monoclonal antibodies that target specific cancer antigens has led to treatments that are more specific to cancer cells, sparing normal tissues. For instance, trastuzumab targets HER2-positive breast cancer cells, which often metastasize to lymph nodes [406]. Second, small molecule inhibitors disrupt cancer cell signaling pathways critical for tumor growth and metastasis [407]. Drugs like imatinib, targeting the BCR-ABL fusion protein in chronic myeloid leukemia, have shown effectiveness in controlling metastatic spread [408]. Third, immune checkpoint inhibitors, such as pembrolizumab, have revolutionized cancer treatment by enhancing the immune system's ability to recognize and destroy cancer cells, including those in lymph nodes [409]. Fourth, advances in gene therapy, such as the use of CRISPR/Cas9 for gene editing, provide new avenues for targeting the genetic alterations specific to metastatic cells [410]. Lastly, nanoparticle-based drug delivery systems enable targeted delivery and controlled release of therapeutics directly to metastatic lymph nodes, improving treatment efficacy and reducing systemic side effects [411]. The ongoing research in these areas continues to expand the arsenal of targeted therapies for cancer metastasis, potentially transforming the prognosis for patients with advanced disease [412].

Fig. 8

The sequence and primary challenges involved in gene delivery for melanoma treatment. This includes the creation of the nucleic acid polyplex, its journey through the bloodstream, gathering at the targeted tissue, movement within the cell, and the release of its contents in the nucleus. Re-printed from the Springer Nature [89]

Emerging technologies in molecular imaging for lymph node metastasis are revolutionizing cancer diagnosis and management [413]. Firstly, advanced PET imaging techniques, such as PSMA-PET for prostate cancer, provide superior specificity and sensitivity in detecting metastatic lymph nodes [414]. Secondly, the development of novel contrast agents for MRI, like iron oxide nanoparticles, enhances the visibility of metastatic lymph nodes [415]. Thirdly, optical imaging technologies, including near-infrared fluorescence imaging, offer non-invasive ways to visualize lymph node metastasis during surgery [416]. Fourthly, photoacoustic imaging, which combines ultrasound and optical imaging, provides high-resolution images of lymph node metastases [417]. Lastly, molecular ultrasound, using targeted microbubbles, allows for the real-time visualization of molecular expressions in lymph nodes [418]. These technologies, by providing more accurate and detailed information about the extent and nature of lymph node involvement, aid in better staging, treatment planning, and monitoring of cancer [419].

Conclusion

The review underscored groundbreaking developments in molecular imaging techniques, which have substantially enhanced the detection and characterization of lymph node metastases. This advancement facilitates earlier, more precise diagnoses, and better staging of cancer, crucial for effective treatment planning. Simultaneously, targeted therapeutics have emerged as a pivotal approach, focusing on the specific molecular profiles of cancers. These therapies have shown promise in reducing the adverse side effects typically associated with traditional cancer treatments and improving efficacy. The integration of advanced molecular imaging and targeted therapeutics holds significant implications for cancer care. Enhanced imaging capabilities lead to improved identification of metastatic nodes, thus enabling more accurate prognoses and tailored treatment strategies. Targeted therapeutics, on the other hand, offer a personalized approach to treatment, potentially improving survival rates and quality of life for patients. These advances represent a shift towards more individualized, precise cancer care, moving away from a one-size-fits-all approach. Looking ahead, nanobiotechnology emerges as a promising frontier in oncology. This field has the potential to further refine the accuracy of molecular imaging and the efficacy of targeted therapeutics. Nanoparticles can be engineered to enhance imaging contrast or to deliver therapeutic agents directly to tumor cells, minimizing systemic toxicity. The future of nanobiotechnology in oncology is poised to usher in an era of highly efficient, minimally invasive cancer diagnosis and treatment modalities. This could revolutionize the management of lymph node metastasis in cancer, offering hope for better patient outcomes.