Tumor antigens bind to MHC-I molecules and are presented on the surface of tumor cells. This renders them recognizable by immune effector cells. Therefore, tumor cells with dysregulated presentation of antigens bound to MHC-I for presentation are more likely to avoid detection by the immune system (8). In general, tumor cells can downregulate the antigen presentation by MHC-I via either deletion of the MHC-Ⅰgene or inhibition of MHC-Ⅰgene transcription. The human MHC genes encodes various molecules expressed on white blood cells called human leucocyte antigen (HLA). The expression of HLA-I antigen is downregulated in most malignant tumors, such as melanoma, gastric cancer (GC), breast cancer and ovarian cancer. Moreover, the degree of this downregulation is positively correlated with the degree of malignancy and metastasis of tumors.

The elimination of tumor cells by the immune system relies on the reaction of immune effector cells to antigens present on the surface of tumor cells. However, tumor cells often exhibit reduced or absent expression of tumor antigens, inhibiting the activation of T cells by dendritic cells (DCs) and evading recognition and destruction by cytotoxic T lymphocytes (CTLs). It has been reported that tumor cells will undergo antigen mutation when co-cultured with monoclonal and polyclonal transgenic CTLs, which specifically recognize the tumor antigen P1A, and thus, P1A is not readily recognized by CTLs (9). In addition to generating antigenic mutations, tumor cells can also evade recognition by the immune system by shedding the antigens expressed on their surface. For example, carcinoembryonic antigen can be shed from the surface of tumor cells, which renders tumor cells unrecognizable by immune effector cells. Similar to the loss of tumor antigens, tumor cells can also evade recognition and attack by NK cells following the release of natural killer cell group 2-member D (NKG2D) ligands (10).

Activation of T cells requires the induction of the first signal produced by the binding of T cell receptors to antigen peptide-MHC complexes, and also the second signal provided by the binding of costimulatory molecules (CMs) on antigen-presenting cells or tumor cells to CM receptors on T cells. Tumor cells that only express MHC-I antigens, but lack CMs participate in the antigen presentation process, but cannot activate T cells and elicit strong immune responses. Such tumor cells can lead to the emergence of immune tolerance (11). The B7 family of molecules and their receptors are the most important CM pairs participating in the activation of T cells. The binding of each molecule to its receptors promotes activation and proliferation of T cells. Studies found that tumor cells downregulated the expression of B7-1 and B7-2 molecules, meaning there is insufficient induction of T cell activation signals such that T cells do not proliferate, whereas the expression of B7-H1 and B7-H4 molecules is upregulated. Once they bind to the receptors, these inhibitory CMs generate inhibitory signals, induce the apoptosis of T cells, and inhibit the antitumor immune response of the body (12,13).

The TME contains numerous immunosuppressive cytokines, including TGF-β, IL-6 and IL-10, which impede antitumor immune responses through direct or indirect mechanisms. TGF-β, for example, hinders the proliferation of immune effector cells, suppresses DC maturation, reduces CTL and NK cell activation, reduces the levels of antitumor immune cytokines such as IFN-γ and TNF-α, and inhibits MHC-II antigen expression induced by IFN-γ in melanoma cells (14). IL-10 can reduce the expression of CMs on DCs, inhibit tumor antigen presentation, alter their phenotypes, inhibit the activity of T cells, and block T cell-mediated attacks on tumor cells. It has been shown that TNF can induce hemorrhagic necrosis of certain tumor blood vessels, specifically eliminate tumor cells, and modulate the immune functions of cells, while tumors can express soluble TNF binding protein, which prevents the eliminating effect of TNF (15). Additionally, vascular endothelial growth factor (VEGF) has been implicated in the development of tumor immune escape mechanisms. As a specific endothelial cell stimulating factor, VEGF can accelerate tumor neovascularization, increase the permeability of blood vessels, and promote the infiltration and metastasis of tumor cells. It can also suppress the maturation of DCs, affecting antigen presentation function, and induce the programmed death ligand 1 (PD-L1) expression in mature DCs, eventually stimulating the T cells and the formation of CTLs (16,17).

The ECM in the TME supports the proliferation and metastasis of tumor cells. The ECM is also an important component of a hypoxic TME is composed of CAFs, TAMs, mesenchymal stem cells (MSCs), inflammatory cells and endothelial cells (18). The ECM is an important non-cellular component of the TME and plays a key role in maintaining tissue structure and function. As a physical barrier of the tumor, the ECM can dissolve drugs or delay drug delivery (19). Fibronectin (FN), hyaluronic acid, collagen (Col) and laminin are the main components of the ECM, and can form ECM fibers. Specific enzymes, such as lysyl oxidase cross-link these fibers, regulating tumor hardness and promoting fibrosis (20). Laminin has been revealed to be highly expressed in multidrug-resistant cells (21,22). Alterations in the ECM can facilitate tumor cell invasion and metastasis, influence the penetration and distribution of chemotherapeutic drugs, and diminish their effectiveness.

Di Martino et al (23) found that type III Col induced tumor cell dormancy in vivo and in vitro experiments, and demonstrated that changes in ECM Col orientation represented the transition from dormancy to reactivation (23). Puttock et al (24) identified that the TAM population associated with cancer immunotherapy and ECM composition and found that tumor ECM can directly educate TAMs found in ovarian cancer tissues that are associated with a poor prognosis, and that targeting ECM can improve immune invasion and immunotherapy sensitivity. Wang et al (25) developed an ECM deprivation system based on FN-targeted self-assembly peptide as a chemotherapy sensitizer, which can significantly inhibit the tumor-promoting effect of ECM, and may become a novel method to inhibit ECM and enhance the sensitivity of chemotherapeutic drugs (25).

During tumor growth, immunosuppressive cells undergo differentiation, proliferation and aggregation at the tumor site, including TAMs, regulatory T cells (Tregs), tumor-associated neutrophils (TANs), myeloid-derived suppressor cells (MDSCs) and tumor-associated DCs (TADCs) (26). Several immunomodulatory factors have been reported to date. In the present review, the main components of the TME and their mechanisms of action were introduced.

TAMs are a special class of macrophages derived from monocytes in the peripheral blood and migrate to tumor tissues. They are an important part of the TME, contributing to the occurrence and progression of tumors by creating an immunosuppressive microenvironment (27). TAMs typically differentiate into one of two activation states: M1 macrophages, which have a tumor-suppressive function, and M2 macrophages, which have a tumor-promoting function (28). M1 macrophages exert proinflammatory effects, eliminate tumor cells and inhibit tumor growth. By contrast, M2 macrophages inhibit inflammatory processes and modulate the immune cells thereby promoting tumor growth, invasion, metastasis and angiogenesis (29). M1 macrophages eliminate cancer cells through antibody-dependent cell-mediated cytotoxicity such as TNF, immune killer molecules and inflammatory cytokines (30). In comparison, activated M2 macrophages have been reported to accelerate the proliferation, invasion and metastasis of tumor cells by enhancing angiogenesis and inhibiting the antitumor function of immune cells (31). VEGF, IL-1, TNF-α, prostaglandin E2, adrenomedullin and brain signaling protein 4D contribute to angiogenesis (32).

By interacting with other cells, TAMs regulate the composition and function of the TME and affect the behavior and characteristics of tumor cells. Indeed, targeting TAMs is being considered as a strategy for cancer treatment. M2 macrophages are also closely associated with tumor angiogenesis and lymphangiogenesis, known to directly modulate tumor proliferation and metastasis, induce tumor drug resistance, and secrete cytokines such as IL-10 and TGF-β, which inhibit immune responses (33). The secretion of PD-L1, cytotoxic T lymphocyte-associat-edantigen-4 (CTLA-4) and other molecules may enhance CTL apoptosis and inhibit CTL activation (34), resulting in immunosuppression.

Chen et al (35) found that Jumonji domain containing 6 (JMJD6) can reduce the growth of Lewis lung carcinoma tumors and B16F10 melanomas by inducing M2 polarization through STAT3/IL-10 signaling, and make tumors sensitive to immune checkpoint blockades (ICBs), which can enhance the treatment potential of ICBs. Tang et al (36) used a transgenic mouse model to effectively combat hepatocellular carcinoma (HCC) by targeting xCT-mediated ferroptosis; it was found that pro-tumoral polarization of macrophages is effective against HCC and enhances the efficacy of the anti-PD-1/L1 response (36). Li et al (37) found that a membrane spanning four domains A4A promotes M2 polarization of macrophages by activating the PI3K/AKT and JAK/STAT6 pathways, which can improve the efficacy of immune checkpoint inhibitor and is a novel avenue for anticancer immunotherapy.

Tregs constitute a subset of immune cells primarily responsible for maintaining immune homeostasis and suppressing the immune response against cancer (38). They achieve this by restraining the activity of other immune cells, thereby preventing excessive immune reactions and the development of autoimmune diseases. Tregs are categorized into two primary types: Natural Tregs (nTregs), which originate in the thymus, and induced Tregs (iTregs), which differentiate in peripheral tissues (39,40). nTregs, also known as thymus-derived Tregs, primarily control the inflammatory response following infection and maintain normal immune tolerance. iTregs, also known as peripherally-induced Tregs (41), can generate immune factors and thereby decrease the activity of immune cells or directly bind to immune cells to inhibit their activity. Tregs are a double-edged sword. They can regulate the strength and duration of the immune response by inhibiting the activity and function of other immune cells to ensure the normal response of the immune system to external antigens and prevent the occurrence of autoimmune diseases. Within the TME, hyperactive Tregs cells can inhibit immune cell assault on tumors, consequently allowing tumor evasion and proliferation (42).

Tregs participate in immune regulation, autoimmune diseases and tumor immune escape among other processes. Further studies into the function and regulatory mechanism of Tregs are required to improve our understanding of the immune balance, occurrence and development of immune-related diseases. This is essential for developing new immunoregulatory therapies. Tregs have been reported to inhibit DCs by expressing IL-10, TGF-β and IL-35, and secrete granzyme and perforin to eliminate effector cells directly, and inhibit the proliferation of effector cells. In addition, Tregs highly express CD39 and CD73 molecules, which increase adenosine production, and bind to adenosine receptors on the surface of effector cells to exert inhibitory effects (43).

Zhang et al (44) proposed that YTHDF2 is essential for Tregs in the TME by regulating transcription of M⁶A-modified NF-κB negative regulators and may serve as a potential drug target for cancer immunotherapy. Wen et al (45) found that salidroside (SAL) can inhibit the function of Tregs and inhibit the proliferation of lung cancer cells by regulating the Hsp70/stub1/Foxp3 pathway in Tregs, which is a new mechanism for the use of SAL in tumor therapy. Shiri et al (46) found that Treg-derived IL-10 upregulates PD-L1 expression in monocytes, which in turn reduces CD8⁺T cell infiltration and associated antitumor immunity in colorectal cancer (CRC)-derived liver metastases. These findings provide the basis for future monitoring and targeting of IL-10 in CRC-derived liver metastases (46).

TANs are a class of neutrophils that are present in the TME. As an important type of cell of the immune system, TANs participate in tumor development and progression. They are functionally divided into tumor-suppressive N1 cells and tumor-promoting N2 cells (47). TGF-β induces N1 to N2 polarization of TANs (48). N1 TANs can activate the effector T cells to prevent tumor development, promote tumor cell apoptosis via tumor necrosis factor-associated apoptosis-inducing ligand, and promote the release of matrix metalloproteinase 8 (MMP8) to degrade the ECM, which favors tumor metastasis (49). Conversely, N2 TANs enhance angiogenesis by stimulating VEGF, facilitate tumor advancement and metastasis through cathepsin G and reactive oxygen species (ROS) (50), and affect tumor aggressiveness and prognosis via various mechanisms. TANs form a complex network alongside tumor cells and other immune cells. They regulate the inflammatory milieu, modulate immune responses, and mediate cell-to-cell interactions within the TME, thereby influencing tumor progression. Investigating the functions and mechanisms of TANs is instrumental in identifying novel therapeutic targets and devising innovative strategies for cancer treatment.

Hu et al (51) performed a single-cell transcriptomic analysis of 81 patients with non-small cell lung cancer (NSCLC) and identified a TAN-promoting cluster with High mobility group box 1 (HMGB1) upregulation that was predicted to suppress tumor immunity and mediate immune escape via the GATA2/HMGB1/TIM-3 axis. Sheng et al (52) found that TAN-derived relaxin-2 (RLN2) promoted the migratory capacity of MCF7 cells via a PIK3-AKT-MMP-9 axis. The analysis of surgical samples from 20 patients with breast cancer found that the presence of TANs in breast cancer supported the invasion and migration of malignant cells (52). Chan et al (53) demonstrated in vivo and in vitro that pancreatic melatonin enhanced antitumor immunity in pancreatic cancer and neuroendocrine tumors by regulating TANs infiltration.

MDSCs, as one of the most important types of stromal cells of the TME, are multifunctional cells derived from the bone marrow, and they exhibit immunosuppressive effects in pathological conditions to protect tumor cells from attack by the host's immune system via the production of ROS to inhibit T cell function (54,55). Their morphology is very similar to that of granulocytes or monocytes. Therefore, the two major populations of MDSCs are called polymorphonuclear neutrophil MDSCs (PMN-MDSCs) and monocyte MDSCs (M-MDSCs). Both types can inhibit the activity of the TME, in which M-MDSC shows significant plasticity and differentiation direction regulated by the TME (56). M-MDSCs may exhibit non-specific inhibition via various mechanisms and secrete various immunosuppressive factors, such as nitrous oxide, granulocyte-macrophage colony-stimulating factor, IL-10 and IL-6, among other factors, which can directly or indirectly inhibit the activity of T cells (57). By contrast, PMN-MDSCs exhibit antigen-specific T cell tolerance and function as non-specific suppressor cells capable of producing cytokines that promote tumor angiogenesis. MDSCs are important regulatory cells in the TME, and their immunosuppressive function influences tumor growth and response to treatment. In-depth studies on MDSCs are required to determine the mechanisms of tumor immune escape and provide new ideas and strategies for individualized and precise treatment. Aggregation of MDSCs can directly stimulate tumor angiogenesis by releasing various pro-angiogenic factors. Moreover, MDSCs can enhance the expression of immunosuppressive factors, including arginase 1, ROS and inducible nitric oxide synthase to induce apoptosis of activated T cells (58-60).

Zhang et al (61) found that C-C motif chemokine ligand 20 (CCL20) can regulate the TME to promote cancer development, especially the interaction between PMN-MDSCs and breast cancer stem cell in breast cancer, and this is hypothesized to underlie novel strategies for cancer treatment. Mei et al (62) found that 1L-37 can inhibit the development of tumors by inhibiting the immunosuppression of MDSCs in the TME through metabolic reprogramming, highlighting it as a novel avenue for cancer immunotherapy.

There is strong evidence indicating that tumors can interfere with the differentiation of monocytes into normal DCs and induce their differentiation into other types of monocytes of the same lineage, thus acting as immunosuppressive cells in the TME. Such cells are called TADCs. The expression of the surface antigen presentation related molecules MHC-I, MHC-II and activation molecules CD80 and CD86, are decreased on TADCs. This decreases its antigen processing and presentation ability. Moreover, TADCs exhibit upregulated expression of signal transducers and activators of transcription protein3 (STAT3), IL-12 transcription, suppression of DC maturation and the activation of T cells (63,64). Bregs, a special subtype of B lymphocytes, can secrete IL-10, TGF-β and IL-35, and promote Treg generation, which also exerts immunosuppressive effects (65).

Factor-associated suicide (Fas) is a crucial death receptor known to trigger apoptosis. Under physiological conditions, T cells can induce apoptosis in Fas-positive target cells via Fas/Fas ligand (FasL)-mediated pathways. However, tumor cells possess mechanisms to evade T cell attacks; They can downregulate Fas expression or harbor Fas mutations, rendering themselves resistant to T cell-mediated apoptosis. Moreover, tumor cells often exhibit upregulated expression of FasL, which binds to Fas receptors on T cells, leading to T cell apoptosis (66). In addition to aberrant expression of Fas/FasL molecules and the development of resistance to apoptosis, tumor cells also exhibit upregulated expression of certain other immunosuppressive molecules and induce apoptosis of immune effector cells. For example, indoleamine2, 3-dioxygenase (IDO), which is upregulated in tumor cells, promotes tryptophan degradation. On the one hand, tryptophan deficiency can result in the arrest of T cells in the G1 phase of the cell cycle and suppress the proliferation of T cells. On the other hand, tryptophan degradation generates metabolites with cytotoxic and pro-apoptotic effects, which inhibit apoptosis-inducing effects on both T cells and NK cells (67). In addition, upregulation of B7-H1 molecule (also known as PD-L1), which is present on the surface of tumor cells, when combined with the T-cell inhibitory receptor PD-1, can induce T cell tolerance. Furthermore, it stimulates the secretion of IL-10 and induces apoptosis of T cells (68,69).

Administration of chemotherapeutic drugs such as paclitaxel promotes the secretion of CSF1 and IL-34 from breast cancer cells, thereby attracting macrophages to infiltrate the TME. Subsequently, this inhibits the activation and proliferation of CTLs, thereby diminishing their antitumor immune capacity. It also inhibits the antitumor effect of cytotoxic drugs (103). Conversely, neutralizing antibodies targeting CSF1 can inhibit TAM infiltration in breast cancer, thereby enhancing the antitumor immune response of CTLs to a certain extent and improving the efficacy of chemotherapy. In lung cancer, the cytotoxic drug doxorubicin (DOX) induces the production of IL-34 from tumor cells through the activation of the NF-κB pathway. IL-34, regulated by EBPβ, augments the immunosuppressive and tumor-promoting functions of TAMs. This prevents CTL responses and promotes regulatory T lymphocyte responses, thereby facilitating tumor immune evasion, maintaining TME homeostasis during chemotherapy, and reducing chemotherapeutic efficacy (104).

Tumor treatments act by improving the CTL response and achieving immune checkpoint blockade; however, certain patients do not respond to programmed death-1/ligand-1 (PD-1/-L1) antibody treatment. TAMs express PD-L1 and CTLA-4 ligands. By binding to PD-1 and CTLA-4 on T cells, they inhibit the immune response of T lymphocytes directly and decrease the efficacy of immunotherapy (105).

IL-6, secreted by TAMs can decrease the levels of the tumor suppressor miR-204-5p by activating STAT3, thereby enhancing the anti-apoptotic ability of CRC cells and the development of resistance to 5-fluorouracil (5-FU) and oxaliplatin (OXA) (106). It has been demonstrated that M2-type TAMs in breast cancer tissues and tumor cells promote the development of tumor resistance to DOX via the paracrine circuit of IL-6 (107). IL-10 is primarily activated and released by M2-type TAMs, which stimulates STAT3 to upregulate the expression of the protooncogene Bcl-2, thereby reducing the apoptotic effect of paclitaxel on breast cancer (108). CCL22, secreted by M2-type TAMs in colorectal tumors can promote epithelial-mesenchymal transition (EMT) of tumor cells and inhibit caspase-mediated cell apoptosis. It can also promote resistance of tumor cells to 5-FU (109).

The hypoxic conditions within GC lesions activate the HIF-1α, thereby increasing the expression of HMGB1. This elevation in HMGB1 levels can facilitate the migration of macrophages to a tumor and stimulate the production of growth differentiation factor 15. Consequently, this process accelerates the oxidation of fatty acid β in GC cells, ultimately promoting tumor resistance (110). It has been revealed that M2-type TAMs induce gemcitabine resistance in pancreatic ductal adenocarcinoma (PDAC) via the insulin-like growth factor (IGF) (111). Cathepsins, a type of cysteine proteinase, participate in the development of cancer drug resistance. Upon activation by IL-4, cathepsins B and S within TAMs are implicated in drug resistance in lung, colon and breast cancer. This mechanism may involve the degradation of drug target proteins by cathepsins.

Macrophages in breast cancer tissues inhibit tumor cell apoptosis and induce autophagy by activating PI3K/AKT/survivin signaling pathway, leading to a reduction in sensitivity of breast cancer cells to DOX (112). TAMs can enhance the anti-apoptotic ability of breast adenocarcinoma cells via the CCL2/PI3K/AKT/mammalian target of rapamycin (mTOR) signaling pathway. This further leads to the development of resistance to tamoxifen (113). In GC, conventional chemotherapeutic drugs such as 5-FU induces GLUT3-dependent glycolysis in M2-type TAMs, which activates the CCL8/Janus kinase1 (JAK1)/STAT3 signaling pathway. It also enhances the tolerance of tumor cells to 5-FU (114). In addition, studies it has been indicated that TAMs in GC can promote drug resistance in tumor cells by activating the HIF1α/leukemia inhibitory factor/STAT3 signaling pathway (115).

It has been indicated that TAMs in malignant tumors contribute to ECM degradation and remodeling by producing MMPs. In addition, TAMs regulate the synthesis and release of pro-angiogenic factors, thereby facilitating tumor blood vessel formation. Stockmann et al (116) found that VEGF derived from TAMs induces tumor resistance to cyclophosphamide by promoting the formation of an abnormal tumor vascular network characterized by low vascular density, low tortuosity and low adventitia cell coverage. In line with this, TAMs induce the formation of abnormal blood vessels with low perfusion by secreting VEGF, limiting the entry of chemotherapeutic drugs into the tumor to exert antitumor effects, and significantly reducing the effect of chemotherapy (117). In lung adenocarcinoma, M2-type TAMs can upregulate VEGF-C expression and its receptor VEGFR3, promoting tumor growth and downregulation of the tumor suppressor genes p53 and PTEN, thereby inhibiting tumor cell apoptosis and reducing their sensitivity to chemotherapeutic drugs (118). In ovarian cancer treatment with anti-VEGF drugs, the expression of VEGFR1 and VEGFR3 in TAMs may decrease. Despite this reduction, TAMs retain their capacity to facilitate tumor cell tolerance to anti-VEGF drugs by activating alternative angiogenic pathways (119).

CSCs, a subset of cancer cells, are multipotent cells with self-renewal and tumor initiation properties. These features contribute to the occurrence, development and drug resistance of tumors. It has been found that the M2-type TAMs can induce tumor cells to acquire stem cell characteristics, thereby promoting the malignant progression of tumors (120). IL-17 in ovarian cancer tissues is primarily derived from TAMs and CD4⁺ T lymphocytes, which bind to the IL-17 receptor expressed on tumor cells with a stem cell phenotype. It can activate the NF-κB/p38 mitogen activated protein kinase (MAPK) signaling pathway, and hence the stem cell characteristics of tumor cells and the promotion of tumor progression and drug resistance (121). Milk fat globulin epidermal growth factor8 and IL-6 secreted by M2 TAMs synergistically activate the transcription factor STAT3 which enhances the stem cell properties of pancreatic cancer cells. They inhibit a CTL immune response, thereby promoting tumor drug resistance, while reducing the infiltration of TAMs and the stem cell characteristics of tumor cells (122). Similarly, TAM-derived IL-10 can also significantly enhance the stem cell characteristics of small cell lung cancer cells by activating the JAK1/STAT1/NF-κB/Notch1 signaling pathway (123).

TAMs can regulate the expression of drug metabolism enzymes intra and extracellularly and alter the metabolic processes mediated by drugs in tumor cells. For example, cytokines secreted by TAMs, such as IL-10 and TGF-β, can upregulate the CYP450 enzyme system in tumor cells, thereby altering the metabolic rate of chemotherapeutic drugs and affecting the activity and half-life of drugs (124). TAMs inhibit the activity of effector T cells and NK cells, thereby weakening the immune system's attack on the tumor. Through these immunomodulatory effects, TAMs indirectly affect the efficacy of antitumor drugs, increasing the likelihood of tumor cell survival and proliferation (125). TAMs promote the degradation and remodeling of ECM by secreting a variety of stroma-degrading enzymes, change the physical and chemical characteristics of the TME, and affect the distribution and metabolism of drugs in tumor tissues (126).

TAMs can promote the repair of DNA damage in tumor cells induced by chemotherapy, promote the proliferation of endothelial cells by secreting certain cytokines such as VEGF and 1L-1, promote angiogenesis, and provide nutrients and oxygen for tissue repair (127). TAMs degrade and reshape the ECM by secreting matrix remodeling enzymes such as MMPs to provide spatial and structural support for the growth and migration of new tissues (128). This promotes cell survival and tissue repair by activating multiple signaling pathways. For example, TAMs can promote the proliferation and survival of tumor cells by secreting epidermal growth factor (EGF) and activating the EGF receptor signaling pathway (129). After chemotherapy, TAMs promote tissue repair by secreting anti-inflammatory factors and immunosuppressive factors that regulate the local immune environment and reduce inflammatory response and immune attack. For example, TAMs reduce inflammatory damage by secreting IL-10 and TGF-β, inhibiting the activity of effector T cells and NK cells (130). Several studies have shown that TAMs can support the survival and proliferation of CSCs by secreting specific cytokines, such as IL-6 and CSF-1. These cytokines can activate key signaling pathways in CSCs, such as JAK/STAT3 and PI3K/AKT, and enhance drug resistance and repair ability of CSCs (131).

Interestingly, Lurbinectedin (PM01183) enhanced the antitumor of gemcitabine in PDAC by exhibiting a specific depletion of TAMs that downregulated cytidine deaminase expression and increased gemcitabine-mediated DNA damage (132). Radioresistance of tumor cells could potentially be one of the causes for local recurrence post treatment. HMGB1 was shown to play a role in bladder cancer radioresistance through its intracellular functions in promoting DNA damage repair and autophagy. Moreover, combining radiation and HMGB1 inhibition significantly impaired tumor infiltrating MDSCs and TAMs-but not Tregs- and shifted the overall tumor immune balance towards antitumor response (133). Hong et al (134) experimentally verified that TAMs enhanced WTAP-mediated N6-methyladenosine RNA methylation through a CXCL16/CXCR6 axis and promoted cisplatin resistance in ovarian cancer cells.

Therefore, TAMs promote tumor drug resistance by modulating the immune microenvironment, cytokines, signaling pathways, angiogenesis and CSCs (Fig. 3).

In CRC, CAFs enhance the secretion of lncRNA H19 by activating the Wnt/β-catenin pathway. This enhances the stemness of CSCs, promoting resistance to OXA in CRC cells (138). Moreover, CAFs induce the expression of Wnt signaling-related genes in CRC cells, such as T lymphoma invasion and metastasis inducing protein-1, mediating resistance to 5-FU (139). In addition, activation of the NF-κB pathway can regulate the self-renewal of CSCs, also contributing to drug resistance (140). In GC, CAFs activate the NF-κB pathway by secreting the neuroregulatory factor 1, and this process is closely related to GC drug resistance and prognosis (141). In addition, CAFs may activate the IL-11/IL-11R/gp130/JAK/STAT3 anti-apoptotic signaling pathway in GC cells by secreting IL-11, to promote the maintenance of chemotherapeutic resistance of CSCs (142). There is evidence that CAFs can secrete TGF-β1 through the Smad2/3 pathway and upregulate the expression of STAT4 in PDAC tumor cells, thereby maintaining the characteristics of CSCs and promoting the resistance of tumor cells to gemcitabine (143).

EMT, regulated by transcription factors such as ZEB and Snail, is a key process that modulates cancer progression. In CRC, the expression of Snail1 in the tumor stroma enhances chemoresistance in tumor cells. As a result, CAFs facilitate the emergence of resistance in CRC to drugs such as 5-FU and paclitaxel by increasing Snail1 expression (144). In addition, CAFs induce EMT of tumor cells by upregulating the expression of cyclooxygenase-2 and prostaglandin E2 synthesis in CRC cells, thereby reducing the sensitivity of CRC cells to OXA (145). In esophageal squamous cell carcinoma (ESCC), IL6, secreted by CAFs, upregulates the expression of CXCR7 in tumor cells and promotes the process of EMT via the STAT3/NF-κB pathway. This suggests that CAFs may affect cisplatin resistance by secreting IL-6 (146).

Exosomes secreted by CAFs promote the occurrence and development of gastrointestinal tumors and chemotherapeutic resistance. The mechanism by which CAFs promote chemotherapeutic resistance is as follows: i) They can deliver molecules that may induce drug resistance: CAF-derived exosomes carry microRNAs (miRNAs or miRs), which can alter the gene expression profile of tumor cells and promote drug resistance by downregulating tumor suppressor genes or upregulating drug-resistance-related genes (147). Proteins contained in exosomes (such as MMPs and TGF-β) can activate signaling pathways within tumor cells, enhancing their viability and drug resistance (148). ii) Regulation of the TME: CAF-derived exosomes create a microenvironment conducive to tumor growth and drug resistance by regulating immune cells, such as inhibiting T cell activity and promoting the accumulation of immunosuppressive cells (149). Factors in exosomes can promote the formation of new blood vessels, provide more nutrients and oxygen to tumor cells, and also affect the distribution and effectiveness of chemotherapeutic drugs by altering the permeability of blood vessels (150). iii) Enhance autophagy of tumor cells: MiRNAs and proteins in exosomes can activate autophagy-related signaling pathways (such as MTOR and AMPK), enhance the survival capacity of tumor cells under chemotherapeutic pressure, and reduce the cytotoxicity of chemotherapy drugs (151).

Zhang et al (152) found that CAF-derived exosome NT-AS1 can regulate HIF-1 expression, enhance the proliferation and metastasis of PDAC cells, and reprogram glucose metabolism. Wang et al (153) used (PDGF-BB) to induce human oral mucosal fibroblasts to transform into CAFs and extract exosomes, and found that CAF-Exo had a stronger ability to promote oral squamous cell carcinoma (OSCC) proliferation. These results suggest that CAF-Exo may possess the ability to immunomodulate and promote OSCC proliferation (153). Miaomiao et al (154) found that miR-21 could transform normal fibroblasts into CAFs, and miR-21 was upregulated in various tumors. Exosomes from CAFs promote angiogenesis by introducing miR-21 into multiple myeloma endothelial cells. Therefore, CAF-derived extracellular miR-21 may serve as a novel diagnostic biomarker and therapeutic target (154).

It has been revealed that cricN4BP2L2 in exosomes secreted by CAFs activates the PI3K/AKT/mTOR pathway by binding to EIF4A3, which then promotes the stemness and OXA resistance of CRC cells (155). In addition, miR-625-3p in exosomes secreted by CAFs may enhance the invasive capacity of CRC cells and promote chemotherapeutic resistance of CRC cells by inhibiting the CELF2/WWOX pathway (156). In PDAC, once taken up by adjacent tumor cells, miR-106b in exosomes secreted by CAFs directly targets tumor protein 53 and induces nucleoprotein 1 to promote tumor cell survival and GEM resistance (157). In addition, in ESCC, IL-6 secreted by CAFs and miR-21 packaged in exosomes upregulates STAT3 expression in tumor cells, promotes the generation of MDSCs of monocytes, and finally enhances the resistance of ESCC cells to cisplatin (158). In HCC, CAF-derived exosomes deliver circ-ZFR to tumor cells and promote cisplatin resistance of tumor cells by inhibiting the STAT3/NF-κB pathway (159).

Emerging evidence indicates that CAFs participate in ECM remodeling through a several pathways, which increases the density and stiffness of tumor tissues compared with normal tissues. The remodeled ECM prevents the entry of chemotherapeutic agents into tumor cells, limiting their therapeutic efficacy. In CRC, CAFs are particularly active in synthesizing ECM, which substantially impedes the penetration of the majority of antitumor drugs into solid tumors (160). In addition, increased adhesion between tumor cells and the ECM can arrest the cell cycle induced by the quiescent state, which promotes the development of drug resistance. Taken together, these findings suggest that the influence of ECM and CAFs on the response to chemotherapy is multifaceted, not only forming a protective barrier to block drug diffusion, but also enhancing anti-apoptotic effects through the integrin and focal adhesion kinase (FAK) signaling pathways, as well as forming a hypoxic environment and increased metabolic stress promoting tumor growth, acquisition of a CSC phenotype and treatment resistance (161).

Considering the therapeutic effects of TAMs, they are not being investigated for potential alleviation/prevention of tumor drug resistance and malignant progression. The combination of TAMs with commonly used chemotherapeutic drugs, targeted therapeutic drugs, or immunotherapeutic drugs can reduce tumor drug resistance and enhance antitumor efficacy. Current antitumor strategies targeting TAMs include: i) Inhibition of macrophage recruitment in the TME; ii) removal of M2 TAMs from the TME; iii) repolarization of M2 TAMs into M1 TAMs; and iv) delivery of antitumor drugs.

Chemokine-chemokine receptor signaling pathways, such as CCL2-CCR2 and CCL5-CCR5, act as the primary mechanisms for recruiting macrophages into the TME. Interventions aimed at blocking this signaling to impede macrophage infiltration into the TME have been investigated in both preclinical models and clinical trials. CCR2 antagonists such as PF-04136309 and MLN1202 have demonstrated efficacy in reducing macrophage infiltration in the TME in preclinical animal studies. Moreover, combining CCR2 antagonists with the chemotherapeutic regimen FOLFIRINOX has been shown to augment CTL immune responses in pancreatic tumors, thereby enhancing the efficacy of chemotherapy and inhibiting tumor progression (191). It has been demonstrated that inhibition of CCL5-CCR5 signaling can enhance the therapeutic effect of tumors such as breast cancer, GC, CRC and pancreatic cancer, and CCR5 antagonists can reduce the tumor burden of GC and inhibit its peritoneal metastasis, ultimately prolonging the survival of patients (192-195). In vitro cell experiments have indicated that CCR5 antagonists can suppress the proliferation of pancreatic cancer cells and cell apoptosis. Moreover, animal transplantation tumor models have also revealed that CCR5 antagonists can alleviate liver metastasis of pancreatic cancer (196). Therefore, CCR2 and CCR5 antagonists combined with conventional chemotherapeutic drugs are promising treatments for cancer.

Targeted depletion of M2 TAMs can promote antitumor immune responses and inhibit tumor growth. Lee et al (197) found that the hybrid peptide MEL-dKLA could target M2 TAMs and induce mitochondrial apoptosis, and had a low affinity for M1 TAMs, T lymphocytes, DCs and other immune cells. Moreover, in vivo experiments have validated its capacity to suppress tumor angiogenesis and decrease tumor burden. CSF-1 plays a pivotal role in the polarization of M2 TAMs. Anti-CSF-1 receptor antibodies AFS98 and M279 have demonstrated efficacy in eliminating M2 TAMs in breast adenocarcinoma by intercepting CSF-1 signal transduction. This intervention not only inhibits tumor cell proliferation but also extends the survival of animal models (198).

Corosolic acid (CA) can inhibit the transcription factor STAT3. Liposome-packaged CA combined with anti-CD163 antibody can target TAMs, downregulate the expression of IL-10 and upregulate the expression of TNF-α, as well as promote the transformation of TAMs into M1 (40). Rodell et al (199) reported that Toll-like receptor 7/8 (TLR7/8) antagonist R848 induced the transformation of macrophages into M1. R848 carried by nanoparticles can repolarize M2 TAMs into M1 TAMs in a variety of tumor animal models, and its combination with anti-PD-1 antibody can significantly improve its antitumor immune ability. Immune-response gene 1 (IRG1) is expressed as TAMs in both human and mouse tumors. It has been demonstrated that deletion of IRG1 in mice can inhibit the growth of multiple tumor types, and IRG1-deficient macrophages represent an effective cell-based therapeutic strategy for cancer treatment (200). N-methyl-D-aspartate receptor (NMDAR) is an ion channel expressed on macrophages, and it was found that blocking the TAM phenotype of NMDAR functional and metabolic changes can improve promotion of antitumor immunity mediated by T cells and NK cells (201).

Due to the strong phagocytic ability of macrophages, their efficient migration to tumor lesions following stimulation by chemokines, TAM-mediated antitumor drug delivery has become an important research focus. In previous studies, macrophages were incubated in the peritoneal cavity containing antitumor drugs in the form of nanoparticles or liposome (LPO), and then injected back into animal models. This caused a significant prolongation of the circulating half-life of drugs, enhanced their antitumor efficacy, and reduced drug toxicity (202). In an animal model of lung cancer transplantation tumor, LPO-DOX delivered by TAMs exhibited higher antitumor efficacy with the advantage of low toxicity (203).

A study of two distinct cohorts comprising over 160 PDAC samples showed that FAK activity was increased in CAFs within PDAC compared with fibroblasts from healthy pancreatic tissue. Moreover, elevated FAK activity in PDAC-associated fibroblasts emerged as an independent prognostic indicator for both disease-free and overall survival in multivariate analysis. This highlights the FAK activity in fibroblasts as a pivotal regulator of PDAC advancement and an independent prognostic marker for PDAC progression (204). In a transcriptomic analysis of OSCC xenografts, four genetic indices including FN1, TGFB2, TGFBR2 and TGFBI were detected as CAF indices and were reported to be strong predictors of survival in binary analysis of different subtypes of patients. Moreover, the CAF index is more powerful than the EMT score in predicting survival outcomes (205). In addition, using independent CAF-related prognostic genes, a model for predicting the prognosis of HCC was established. Furthermore, the immune infiltration characteristics, chemosensitivity and immunotherapeutic response of TME were analyzed. The prognostic value the of CAF-related genes was also determined (206). CAFs can resist the immunosuppressive effects and related mechanisms of PD-1/PD-L1 immunotherapy. Researchers have identified several key molecules, such as TGF-β, Ln-γ2, Wnt2 and exosomes. Therapeutic strategies targeting CAF biomarkers are currently in clinical trials with the aim of improving patient survival (207). LncRNA Disheveled binding antagonist of beta catenin3 antisense1 (DACT3-AS1), a CAF derivative, targets miR-181a-5p/SIRT1. OXA resistance-induced downregulation of DACT3-AS1 in CAFs-derived exosomes enhanced OXA resistance through miR-181a-5p/SIRT1 signaling pathway in GC (208).

Tumor response to drug exposure is largely affected by TME, which can reduce the efficiency of chemotherapy drugs and limit the efficacy of immunotherapy. Some clinical findings have shown that targeting TME can enhance the efficacy of chemotherapeutic drugs and immunotherapy. Emerging evidence demonstrated that targeting CAFs can improve cancer chemotherapy by increasing intratumoral drug uptake. Loeffler, a kind of fibroblast activation protein of the oral DNA vaccine, can reduce the expression of type 1 Col, increasing the absorption of the tumor cells to chemotherapy drugs by 70%. Compared with the control group, the life span of the vaccinated mice was 3-fold longer, and the tumor growth was significantly inhibited (209). A pooled analysis of 3,771 patients treated with neoadjuvant therapy found that the pathological complete response (PCR) of breast cancer was 31%, and lymphocyte infiltration of the PCR was only 2% of breast cancer. The presence of CD3 or CD20 lymphocyte infiltration and a low proportion of CD146⁺CAFs indicate higher chemotherapy sensitivity (210).

Among 1,201 patients with NSCLC treated with PD-(L)1 blockade, acquired resistance is common, occurring in >60% of initial responders. Memon et al (211) found that the relapse of tumor can be raised by IFN-γ reaction gene or stable expression to separate. Persistent inflammation of the acquired resistant TME, rather than elimination or abandonment, may provide a new strategy for reversing drug resistance (211).

Ferroptosis is an iron-dependent mode of programmed cell death characterized by the accumulation of lipid ROS to manipulate cancer cell mutation and drug resistance through the lipid metabolic pathway that aggregates on phospholipid glutathione peroxidase. Zhu et al (212) found that ferroptosis achieves lethal levels by accumulating ROS and LPO products in the TME, and ferroptosis-driven nanotherapeutics can reverse drug resistance, showing superior efficacy over traditional methods. Preparation of paclitaxel-loaded ginsenoside Rg3 liposomes has been shown to inhibit the 1L-/STAT3/p-STAT3 pathway for tumor cells and the double effect of TME remodeling, realizing the high tumor inhibition rate of 90.3% (213).