H. pylori is a microorganism capable of surviving in the acidic environment of the stomach and is one of the major risk factors for gastric cancer. There are two main mechanisms of H. pylori’s impact on tumorigenesis: indirect inflammatory responses on the gastric mucosa and direct epigenetic effects on gastric epithelial cells caused by Helicobacter pylori infection (15). Several virulence factors of H. pylori, such as CagA or VacA, increase the risk of gastric cancer (GC). The expression of CagA and VacA in H. pylori is associated with a stronger tissue reaction and a higher risk of precancerous and malignant lesions in the distal stomach (16, 17). Numerous epidemiological studies have shown that H. pylori infection is a risk factor for the development of GC. Additionally, H. pylori infection can damage the gastric tissue microenvironment, promote epithelial-mesenchymal transition (EMT), and further the progression of GC (18).

Genetic factors play a significant role in the development of gastric cancer. Many studies have revealed a clear family history of gastric cancer (19). However, in countries with increased disease incidence, environmental factors have a greater impact on the development of familial GC than genetic changes.

Long-term intake of high-salt, smoked, and cured foods, as well as foods containing nitrites, can increase gastric cancer risk (20). Long-term smoking and alcohol use are also significant risk factors, with smokers having a 50% higher risk of gastric cancer. Additionally, prolonged exposure to chemicals like asbestos and nickel can increase the risk of gastric cancer.

Gastric polyps, chronic atrophic gastritis, and the remnant stomach post-gastrectomy may involve chronic inflammation, intestinal metaplasia, or atypical hyperplasia of the gastric mucosa, potentially leading to cancer (21).

Cancer cells transfer mitochondria with mtDNA mutations to tumor-infiltrating lymphocytes (TILs), resulting in T cell metabolic dysfunction and loss of function, which weakens anti-tumor immune responses and promotes the progression of gastric cancer (22).

H. pylori infection indirectly affects thymidine kinase (TK1) activity by inducing abnormal proliferation of gastric mucosal cells and disrupting DNA synthesis. As a rate-limiting enzyme in DNA synthesis, TK1 activity is closely linked to cell proliferation, bacterial growth, and the host microenvironment. Clinical studies have shown significantly elevated serum TK1 levels in patients with H. pylori-associated precancerous lesions (lung, esophagus, gastric, head and neck, and thyroid), likely reflecting compensatory proliferation following gastric mucosal injury (25).

H. pylori infection promotes uncontrolled proliferation of gastric epithelial cells by disrupting cell cycle checkpoints. Key mechanisms include:

Activation of Cyclin-Dependent Pathways: CagA-positive strains activate the Wnt/β-catenin signaling pathway, upregulate cyclins (e.g., Cyclin D1, Cyclin E) and drive cells into the S phase (26, 27). Since TK1 is a marker enzyme of the S phase, its activity may be synchronously upregulated during this process. Abnormal regulation of the cell cycle directly affects TK1 expression, as TK1 plays a crucial role in DNA synthesis and cell cycle progression (28). Therefore, H. pylori infection upregulates TK1 expression by affecting the expression of cell cycle proteins and the function of cell cycle checkpoint proteins, thereby accelerating cell proliferation and potentially promoting tumor development.

Interference with Inflammatory Signaling: H. pylori infection transcriptionally activates SOD2 via the NF-κB pathway, contributing to 5-FU resistance (29, 30), suggesting a synergistic role for TK1 in bacterial-host metabolic crosstalk. On the other hand, research has shown that activation of the PI3K/Akt pathway can enhance TK1 activity, promote cell proliferation and survival, and provide favorable conditions for the development of H. pylori-related tumors (31). In summary, H. pylori infection significantly regulates the expression of TK1 through the interaction of multiple signaling pathways, thereby affecting cell proliferation and tumorigenesis.

The chronic inflammatory microenvironment induced by H. pylori infection indirectly modulates TK1-related pathways. Bacterial toxins impair the DNA damage response system, exacerbating genetic mutations and carcinogenesis (32). This replication stress may activate TK1-mediated nucleotide salvage synthesis. Besides, H. pylori infection upregulates DNA methyltransferase (DNMT) activity in gastric epithelial cells, leading to hypermethylation of tumor suppressor gene promoters (e.g., p16) (33). Although direct evidence of TK1 gene regulation is lacking, epigenetic modifications of proliferation-related genes may alter TK1 function via metabolic remodeling.

In summary, H. pylori drives TK1 dysregulation through both genotoxic (DNA damage) and epigenetic mechanisms, creating a permissive environment for gastric carcinogenesis. Future investigations should directly examine the epigenetic regulation of the TK1 gene itself during infection and explore the potential of combining TK1 activity monitoring with demethylating agents as a novel strategy to intercept the progression from H. pylori-induced inflammation to gastric cancer.

Drug-resistant H. pylori strains pose significant challenges in treating peptic ulcers and gastric cancer (34). Emerging evidence suggests:

TK-Related Gene Mutations and Resistance: Mutations in herpes simplex virus (HSV) thymidine kinase (TK) genes confer acyclovir resistance (35–37), while zidovudine resistance in Escherichia coli correlates with TK inactivation (38), implying that altered TK activity may influence antibiotic susceptibility.

Novel Hypothesis for H. pylori Resistance: We hypothesize that H. pylori may enhance TK1 enzymatic stability by forming TK1-bacterial complexes or accelerate cell cycle progression through non-canonical pathways, thereby evading antibiotic eradication (Figure 1). Targeting TK1 activity regulation could offer novel strategies to overcome resistance.

Future research should focus more on the functional characteristics of TK1 across different stages of H. pylori infection and on its molecular regulatory network. At the same time, researchers should strive to reconcile differences across studies to develop a comprehensive understanding of TK1 in the pathogenesis of gastric diseases.

TK1 drives DNA salvage synthesis, critically supporting proliferation in differentiated GC (40). In addition, TK1 activity is a vital determinant of FLT uptake in gastrointestinal cancer (41). Growth factors(GF) promote tumor development through TK1-mediated DNA synthesis and glycolysis (42). Through a study on adrenocortical carcinoma, we can infer that the overexpression of TK1 not only serves as a byproduct of the cancer process but also as a crucial part of the selection process, helping cancer cells progress (43).

Research has indicated that Th2 cells display the closest correlation with TK1 among all kinds of immune cells in Pan-cancer. In vitro experiments showed that TK1 affects cancer cell proliferation by regulating G0/G1 phase arrest. Besides, TK1 in cancer cells was also found to regulate Th2 cell polarization through the chemokine CCL5 (44), which is closely associated with gastric cancer cells immune escape since its high expression is a potential indicator for immune evasion of renal cell carcinoma (45).

TK1 is also associated with resistance of gastric cancer cells to 5-fluorouracil(5-FU). Mori et al. found that FdUMP triggers 5-FU resistance by reducing the thymidine phosphorylase-thymidine kinase (TP-TK) pathway, blocking 5-FU incorporation into nucleic acids, and that TK overexpression may play a significant role in the 5-FU resistance of these cells (46). TK is a key enzyme that activates FTD in cancer cells; cells lacking TK activity are less sensitive to FTD (47).

A study on lung cancer has shown that TK1 could promote peritumoral angiogenesis and provide a nutrient and metabolic basis for the growth of tumor cells (48). Although there is currently no research to confirm this, many have speculated that TK1 may be associated with T cell exhaustion and macrophage polarization.In the tumor microenvironment, the dynamic regulation of local oxidative stress is closely related to the metabolic reprogramming of cancer cells. H. pylori binds to free heme released from hemoglobin, inducing an increase in reactive oxygen species (ROS) levels, and in turn activates oxidative stress-related signaling pathways such as nuclear factor kappa B (NF-κB) (49–51). Emerging evidence indicates that this oxidative-stress microenvironment can significantly upregulate TK1 expression (52). The activation of TK1 may form a positive feedback loop with cell cycle regulators via the PI3K/AKT/mTOR signaling axis, further promoting the abnormal proliferation of tumor cells. Notably, pro-inflammatory factors secreted by tumor-associated macrophages under hypoxic conditions may synergistically enhance this effect. At the same time, the imbalance in ferroptosis-related pathways may also exacerbate oxidative stress-induced activation of TK1. This multi-dimensional regulatory mechanism provides a new intervention strategy for TK1-targeting tumor therapy.

As a tumor biomarker, the serum level of TK1 is a reliable indicator of tumor cell proliferation activity and tumor burden, with clear clinical application value. Whether TK1 actively participates in regulating nucleotide metabolism, influences DNA damage repair, and intervenes in key signaling pathways, thereby directly promoting tumor proliferation, survival, invasion, and resistance to chemotherapy (especially antimetabolites) remains unclear. Current research primarily provides correlative evidence. Whether TK1 acts as a core driver oncogene in gastric cancer remains to be confirmed through in vivo and in vitro functional experiments. Recent studies suggest that TK1 mainly functions as a marker of cell proliferation rather than a direct oncogenic driver. TK1 catalyzes the phosphorylation of thymidine in the DNA salvage synthesis pathway, but there is no direct evidence that it induces malignant transformation (6). Although TK1 is overexpressed in various tumors (such as prostate cancer and lymphoma), and its serum levels are associated with tumor stage and prognosis, no TK1 gene mutations or structural activation directly linked to tumor development have been discovered (53). Research has shown that TK1 knockdown can inhibit tumor cell proliferation; however, this effect is primarily attributed to its inhibition of DNA synthesis rather than to the regulation of oncogenic signaling pathways (54). Therefore, TK1’s tumor-promoting role may be indirect, depending on its biological function in supporting proliferative metabolism (55).

In future research, the specific role of TK1 across different tumor types and its synergistic interactions with other signaling pathways will be important areas of focus. In addition, in-depth exploration of the interaction between TK1 and other key signaling pathways may reveal more potential therapeutic targets, providing a basis for the development of personalized treatment plans.

The STK1 assay demonstrates high specificity in oncological screening, with 87% of STK1-positive individuals exhibiting malignancy-associated pathologies (56). Clinically employed TK1 detection methods encompass radioisotope-based labeling (57), immunoblotting, immunohistochemistry (IHC), chemiluminescent dot blot assays, and enzyme-linked immunosorbent assay (ELISA) (58).

As a biomarker of cell proliferation, TK1 has shown promising potential for diagnosing of gastric cancer in recent years. Recent data suggest that serum levels of TK in digestive tract cancer patients are significantly higher than those in normal people, and significant differences have been observed between patients with and without metastatic tumors (59). Serum TK1 may be elevated in conditions of massive cell proliferation, such as infection, inflammation, and malignancy (42, 60, 61). Therefore, TK level detection is a valuable indicator for tumor diagnosis, tumor malignancy, and prognosis observation. A comparative analysis of serum TK1 levels in patients with gastric ulcers, gastritis, gastric polyps, and gastric cancer revealed significantly elevated TK1 levels in malignant cases compared with healthy controls and benign gastric disease cohorts. Further analysis of the receiver operating characteristic (ROC) curve demonstrated optimal diagnostic performance for gastric cancer at a serum TK1 threshold >95.59 μg/L, yielding sensitivities of 83.3% and 70.0% in distinct validation cohorts. These findings underscore the robust diagnostic potential of serum TK1 as a non-invasive biomarker for discriminating gastric malignancies from non-neoplastic conditions (62).

Serum TK1 concentration and TK1 expression in tissues by immunohistochemical staining and chemiluminescent dot blotting, respectively, suggesting that TK1 expression is positively correlated with tumor stage and grading (63). Immunohistochemical detection of TK1 can be used to distinguish between benign from malignant tumors. By measuring serum TK1, clinical doctors can detect significant differences in the proliferation of benign and malignant tumor cells (64).

The study by Liu et al. has demonstrated that changes in TK1 levels during chemotherapy for advanced gastric cancer are closely associated with objective efficacy: a decrease in TK1 after treatment indicates disease remission and longer progression-free survival or relapse-free survival, while an increase in TK1 suggests disease progression. Dynamic monitoring of TK1 changes is more valuable than baseline levels for early prediction of chemotherapy response and survival outcomes in breast cancer (65).

The expression level of thymidine kinase 1 (TK1) in gastric cancer patients is significantly correlated with their survival. Elevated TK1 levels in the serum of gastric cancer patients are associated with the malignancy, degree of differentiation, and clinical staging of the tumor, as well as poorer postoperative outcomes (24). A study on rectal cancer have reported significantly higher serum TK1 levels in patients with poor prognosis, metastasis, advanced TNM stage, lower differentiation, and lymph node metastasis (66).

Although TK1 has a sensitivity of 80%(95% CI: 75-85%) and a specificity of more than 90% in human with breast cancer (67), its non-specific elevation is still seen in chronic inflammation, benign tumors, and metabolic diseases (such as fatty liver, gout, etc.), resulting in a high false-positive rate and limiting its application in the diagnosis of a single marker.

Existing detection methods (such as ELISA and CLIA) have fluctuating sensitivity due to differences in reactant affinity (68), and there are differences in TK1 activity in patients with different malignant tumors; for example, the specificity of serum TK1 measured by Western blotting in MDS patients is significantly higher than that in breast cancer and prostate cancer patients (6).

By inserting the thymidine kinase (TK) gene into Bifidobacterium via genetic recombination, researchers generated a recombinant strain. Once inside the human body, this recombinant strain can colonize tumors and express TK, which phosphorylates the non-toxic prodrug ganciclovir (GCV) into a toxic drug, killing tumor cells specifically. A recombinant Bifidobacterium TK-GCV gene-directed enzyme prodrug therapy (GDEPT) system can effectively induce tumor cell apoptosis, and the mechanism involves activation of the FasL and TNFR2 signaling pathways. It significantly suppresses solid tumor growth without notable toxicity to normal tissues, offering a promising anti-tumor therapeutic strategy and new insights into the treatment of solid tumors (76). Intravenous injection of the BF-rTK/GCV system, mediated by Bifidobacterium and involving herpes simplex virus thymidine kinase, is a safe and effective cancer gene therapy. It elicits a weaker cytokine response than intramuscular injection and inhibits vascular endothelial growth factor (VEGF) expression in mouse models, significantly suppressing gastric tumor growth while ensuring host safety (77). The Bifidobacterium-mediated TK/GCV GDEPT system represents a highly promising and tumor-specific strategy with significant efficacy and an excellent safety profile in preclinical models. Future research should prioritize translational studies, including rigorous toxicology and pharmacokinetic evaluations in larger animal models to pave the way for clinical trials.

Using advanced adenoviral vector technology to carry the TK gene, this system allows adenoviruses to infect cells and deliver the TK gene into the cell interior, where it is expressed. The expressed TK phosphorylates nucleoside analogs, selectively killing tumor cells and enhancing the immune response (78). This gene-directed enzyme prodrug therapy (GDEPT) system is highly efficient and targeted.

Immonen et al. Immonen et al. have shown that GDEPT expressed within tumor cells phosphorylates it, generating toxic metabolites that selectively kill tumor cells. This GDEPT system demonstrated highly efficient targeting and anti-tumor activity in clinical trials, confirming its clinical value in the treatment of malignant tumors (79).

Adenovirus-mediated TK/GCV GDEPT represents a highly efficient and targeted therapeutic strategy with confirmed clinical efficacy. Future research should focus on expanding its application to other solid tumors and overcoming the current limitations of adenoviral vectors, particularly their immunogenicity and poor penetration in dense tumor tissues.

This system contains CD (cytosine deaminase) and TK (thymidine kinase) suicide genes. The CD gene converts 5-fluorocytidine (5-FC) to toxic 5-fluorouracil (5-FU), while the TK gene phosphorylates GCV into a cytotoxic drug. This dual suicide gene system attacks tumor cells from two angles, improving therapeutic efficacy (80–82).

Freytag et al. conducted a phase I clinical trial to evaluate the therapeutic effect of replication-competent adenovirus-mediated dual suicide gene therapy on locally recurrent prostate cancer. The study results showed that the therapy had a favorable safety profile, and tumor volume reduction and disease stabilization were observed in some patients. Although the sample size was limited, the preliminary data suggested that this strategy had potential clinical value in the treatment of refractory prostate cancer, providing a basis for subsequent dose optimization and combination therapy (83).

The CD/TK dual suicide gene system demonstrates enhanced antitumor efficacy through complementary mechanisms of action and a favorable safety profile in early clinical trials. Future research should focus on optimizing viral delivery systems to enhance tumor-specific targeting and transduction efficiency, thereby leveraging potential synergistic effects and addressing tumor heterogeneity.

The recombinant adenoviral vector was able to specifically express the herpes simplex virus thymidine kinase (HSV-tk) gene in carcinoembryonic antigen (CEA)-producing gastric cancer cells by using the CEA promoter, which can accurately transfer the HSV-tk gene to cancerous cells and make them sensitive to GCV, thereby specifically killing gastric cancer cells (84).

Tanaka et al. (85, 86)showed in vivo and ex vivo experiments that the efficiency of AdCEAlacZ-mediated gene transfer correlated with the amount of CEA produced by each cell line. When tumors contained more than 20% AdCEAtk-infected cells, tumor growth was inhibited after GCV treatment, indicating a practical bystander-killing effect. By intratumoral injection of AdCEAtk, HSVtk was selectively expressed in approximately 30% of CEA-producing cancer cells. By injecting AdCEAtk and GCV administration, tumor growth was significantly inhibited by 20% compared with untreated tumors.

In conclusion, the CEA promoter-driven adenoviral system demonstrates a significant therapeutic effect through both direct and bystander killing mechanisms. Exploring the combination of this targeted gene therapy with conventional chemotherapy or immunotherapy could further improve its clinical efficacy for gastric cancer treatment.

Isomoto et al. (87) developed a Hsp70B gene promoter-directed HSV-tk (HSP-tk)/GCV system. The Luciferase assay suggests highly inducible, tumor-specific promoter activity in vitro and in vivo. Synergistic effects were also observed when HSV-tk/GCV, mediated by the non-heat-inducible cytomegalovirus (CMV) promoter, and heat treatment were combined, indicating bystander killing. HSP-tk/GCV carrying HVJ liposomes combined with hyperthermia significantly inhibited the growth of subcutaneous tumors in mice with peritoneal carcinoma and prolonged survival. The combination of suicide gene-directed enzyme prodrug therapy (GDEPT) and hyperthermia may provide a promising treatment for advanced gastric cancer. The HSP-tk/GCV system shows an innovative thermo-responsive gene therapy approach that demonstrates significant anti-tumor efficacy through heat-inducible promoter activation. Clinical translation efforts should optimize hyperthermia parameters and delivery systems (e.g., improved liposomal formulations) to maximize therapeutic outcomes for peritoneal carcinomatosis.

PEG-PEI was used as a carrier and combined with ferroferric oxide Fe₃O₄ magnetic nanoparticles to construct a nanostructured system with specific functions. The nanoparticles can target the tumor site via magnetic field effects and may inhibit the proliferation of BGC823 gastric cancer cells by modulating intracellular signal transduction pathways or metabolic processes. Thymidine kinase may play a synergistic role in this nanosystem, such as regulating signal transduction pathways related to cell proliferation (88). This PEG-PEI/Fe3O4-based magnetic nanosystem potentially leverages both physical targeting and biochemical modulation of tumor cell proliferation for targeted therapy. Further investigation is needed to optimize the nanoparticle formulation for enhanced tumor targeting and therapeutic efficacy, thereby maximizing antitumor activity while minimizing systemic toxicity.

Zhou et al. (89) designed a gastric tumor-targeted ultrasound-triggered phase-change nano-ultrasound contrast agent PAHL-Affibody complex. Using ultrasound-targeted microbubble destruction technology and the nuclear localization effect of the AGM-CBA vector, the suicide gene encoding thymidine kinase was transfected into gastric cancer cells. By combining multiple technologies, the efficiency of gene transfection was enhanced, and thymidine kinase played a more effective role in gastric cancer cells, leading to significant apoptosis. The PFH/AGM-CBA/HSV-TK/Liposome-Affibody nanoultrasound contrast agent was developed, offering new ideas for the treatment of ErbB2-positive gastric cancer. The multifunctional ultrasound-triggered nanoplatform achieves enhanced transfection efficiency through the innovative combination of ultrasound-mediated destruction and nuclear-localizing vectors. Future research should focus on optimizing ultrasound parameters and irradiation protocols to maximize gene delivery while minimizing tissue damage.

Rauf et al. (90)constructed a hybrid nanochannel sensor integrated with DNA, which was used to detect the activity and inhibition of TK1. Single-stranded DNA containing thymidine was used as a substrate, and functional treatment was used to limit the ion current in the nanochannel. Upon kinase action, the thymidine residues at the end of the substrate DNA were phosphorylated, increasing transmembrane ion current, thereby increasing surface charge density and alleviating pore blockage. The hybrid nanodevice can accurately monitor kinase-mediated phosphorylation reactions and demonstrates efficient, specific evaluation in human serum samples. This nanochannel-based biosensor offers a highly sensitive and specific platform for monitoring phosphorylation events in complex biological samples. Future research should focus on validating this detection platform in larger clinical cohorts to establish its diagnostic utility for early cancer detection and monitoring.

A polydopamine-based nucleic acid nanoprobe (PDA-DNA) has been developed to enable precise imaging and treatment of tumor cells by targeting TK1 mRNA (91). The probe uses a catalytic hairpin assembly (CHA) reaction to amplify the fluorescent signal with a detection limit as low as 9.34 pM, which is two orders of magnitude more sensitive than traditional non-amplified probes. At the same time, under 808 nm laser irradiation, the nanoprobe can generate local high temperatures and induce tumor cell apoptosis, thereby achieving synergistic imaging and photothermal therapy (91). PDA-DNA achieves exceptional sensitivity in TK1 mRNA detection while integrating precise imaging with photothermal treatment capabilities. Further development should aim to optimize the photothermal conversion efficiency and targeting specificity, explore combination therapies with chemotherapeutic agents or immunotherapies to enhance antitumor effects.

Another study designed intelligent nanomachines (D/UCNMs) to simultaneously respond to two tumor markers, TK1 mRNA and glutathione (GSH), via an “AND” logic gate, thereby activating near-infrared light-triggered photodynamic therapy (PDT). The system uses specific recognition of TK1 mRNA, combined with enzyme-free amplification technology, to significantly improve the spatiotemporal accuracy of treatment and to monitor drug distribution in real time via NIR-II fluorescence imaging (92). This “AND” logic gate-controlled nanoplatform achieves unprecedented specificity through dual-marker recognition while integrating real-time monitoring with targeted photodynamic therapy. Future research should focus on validating this sophisticated system in vivo to evaluate its targeting efficiency and therapeutic outcomes in complex tumor microenvironments.

Azatian A et al. (93) found that the herpes simplex virus thymidine kinase gene (HSV-tk) can be a suicide gene when combined with the precursor drug ganciclovir (GCV). Introduction of the HSV thymidine kinase gene using an HSV vector, followed by GCV administration, resulted in significant cell death in vitro and tumor regression in vivo. Comparison of the sensitivity of different cell lines, human gastroesophageal junction adenocarcinoma cell line SK-GT-515, and human gastric adenocarcinoma cell line MKN-74 to ganciclovir (GCV). It is suggested that thymidine kinase responds differently to drugs in different cellular contexts, which may be related to intracellular signaling and gene expression regulation. This comparative study may provide a basis for selecting suitable cell models for drug screening and research. The study confirms the therapeutic potential of HSV-tk/GCV suicide gene therapy while highlighting the critical importance of cellular context in determining treatment response. Future research should focus on elucidating the precise molecular mechanisms underlying these cell-type-specific differences, particularly the role of intracellular signaling pathways and gene expression networks that modulate TK-mediated drug sensitivity.

Qiang Li et al. (94) investigated the inhibitory effect of the KDR promoter-driven adenovirus-mediated fusion gene system on the proliferation of human gastric adenocarcinoma SCG7901 cells in vitro. The CDglyTK fusion gene system driven by the KDR promoter could specifically function in cells with high KDR expression, such as SCG7901 and ECV304 cells. The fusion gene system inhibits cell proliferation by expressing components such as thymidine kinase. It exhibits a bystander effect in vitro, i.e., it not only kills cells expressing the system but also inhibits the surrounding untransfected cells. The KDR promoter-driven CDglyTK fusion gene system demonstrates excellent tumor-specific targeting and potent anti-tumor efficacy through dual suicide gene expression. Future research should focus on optimizing the transcriptional targeting strategy by exploring tumor-specific promoters with even greater specificity and activity to create synergistic anti-tumor effects that target both tumor cells and their vascular microenvironment.

Targeted therapeutic strategies against thymidine kinase 1 (TK1) are transforming cancer treatment by disrupting its functional network. In gene-directed enzyme prodrug therapy (GDEPT), recombinant adenoviral vectors such as AdCEAtk deliver exogenous TK1 genes into gastric cancer cells, leading to specific overexpression. This process converts the non-toxic prodrug GCV into its active form, GCV-TP, which damages DNA and triggers apoptosis.

Additionally, the toxic metabolite spreads to neighboring tumor cells through intercellular gap junctions, expanding the treatment’s reach. Meanwhile, PEG-PEI/Fe3O4 nano-delivery systems target tumor tissues with magnetic precision, releasing TK1 inhibitors that block dTMP synthesis. This blockage disrupts the nucleotide pool, halting S-phase DNA replication and curtailing cell proliferation.

Furthermore, TK1 inhibitors, such as GCV analogues, competitively bind to TK1’s active site, stifling its function and leading to dTMP depletion. Together, these strategies not only target TK1’s enzymatic activity but also initiate a multifaceted attack against tumors by modulating various signaling networks, marking a significant advance in oncology.

Future research should focus on developing next-generation TK1-targeting platforms with enhanced tumor specificity and reduced off-target effects, and conducting comprehensive translational studies to bridge the gap between preclinical efficacy demonstrations and clinical application in gastric and other TK1-overexpressing cancers.