The prevalence of CAFs throughout the malignant transformation, from early to late stages, implies that they play an indispensable role in tumorigenesis and progression (Erez et al., 2010). The heterogeneity data demonstrates that the proximal CAFs are empowered with potent juxtacrine TGFβ signaling those aids in transformation into stem cells (Bellomo et al., 2016; Fiori et al., 2019; Nakano et al., 2019; Sahai et al., 2020a). Additionally, the neoplastic cells educate the CAFs to become able to assist through tumor progression and dissemination in other parts of the body (Sahai et al., 2020a; Loh and Ma, 2021; Ping et al., 2021).

Hypothesizing that CAFs foster the niche by enriching the pro-tumor factors, an evidence-based study illustrated that an enhanced expression of TGFβ1 in a CAF-conditioned medium (CAF-CM) remained fundamental to the mesenchymal transformation of the non-CSC bladder cancer cells (Zhuang et al., 2015). Cancer cells induce pro-tumor CAF to establish a pro-favorable niche. TGFβ3 produced from head and neck squamous cell carcinoma (HNSCC) cells can stimulate CAFs to release POSTN, an ECM protein, augmenting the inclination of neoplastic cells towards altered plasticity and metastasizing (Qin et al., 2016; González-González and Periostin, 2018). CSC markers and stemness genes are elevated due to the binding of CAF-derived POSTN to protein tyrosine kinase 7 (PTK7) (Yu et al., 2018a). Likewise, prostate cancer cells turned externally administered bone marrow-derived mesenchymal stem cells (MSCs) into CAFs by TGFβ1 (Barcellos-de-Souza et al., 2016). Interestingly, these stem cell-derived CAFs can change the TME into an M2 (macrophage) phenotype dominant one by transforming residual monocytes. These CAFs can also release cardiotrophin-like cytokine factor (CLCF1) that primarily acts through the JAK-STAT pathway in a positive feedback loop to produce TGFβ and C-X-C motif ligand 6 (CXCL6) (Song et al., 2021). This positive feedback mechanism engages the CAFs to induce stemness by plentiful TGFβ in the TME (Song et al., 2021). In another example citing the role of CSCs in augmenting stemness factors in the TME, a similar paradigm comes into play to employ CAFs by CD24⁺CD49f^hi breast CSCs that trigger the production of components of ECM and pro-tumor paracrine factors in CAFs (Valenti et al., 2017). Valenti et al. (2017) (Valenti et al., 2017) demonstrated that Sonic hedgehog (Shh) derived from breast CSCs were responsible for activating CAFs that, in turn, supplemented the stemness (Valenti et al., 2017; Cazet et al., 2018). Recent research on the origins of chemotherapy resistance found IL-34 and macrophage colony-stimulating factor-1 (M-CSF-1) to be two of those (Baghdadi et al., 2018; Hama et al., 2020). IL-34, with the help of M-CSF-1, acted in a pro-survival way for the tumor cells by helping the monocytes grow alongside converting NFs to CAFs. These CAFs can transform these monocytes into immunosuppressive M2 macrophages, besides secreting stemness-promoting factors like Netrin-1 and FGF2 protein (Suh et al., 2016; Sung et al., 2019). The conversion into the M2 phenotype also inhibits the cytotoxicity of tumor antigen-specific CD8⁺ T-cells (Baghdadi et al., 2016; Giulianelli et al., 2019; Sung et al., 2019; Blondy et al., 2020). Other examples involve in vitro data, suggesting that the influence of HNSCC cells on the CAFs to produce Wnt3a increases cancer stemness (Le et al., 2019).

CAF-derived factors play critical roles in developing and maintaining CSCs by boosting stemness pathways. Hepatocyte growth factor (HGF), released by stromal cells, like fibroblasts, dramatically enhances stemness and EMT gene expression by increasing the expression of CD44⁺, CD47⁺, and CD90⁺ markers tissue (Yan et al., 2018a; Ding et al., 2018). A rise in the stemness markers and an increase in spheroid formation were demonstrated to be due to the activity of CAF-derived IL-6 through the STAT3 pathway (Xiong et al., 2018; Zhang et al., 2020). Other well-known stemness factors, like NANOG and ALDH, are similarly enhanced by the AKT pathway, which is controlled by the CAF secretome (Li et al., 2018). Furthermore, CAF is a crucial modulator of EMT in cancer cells due to the release of IL-6 (Raskov et al., 2021). A few other molecules causing EMT and stemness are Serglycin (SRGN), Annexin A1 (AnxA1), and Prostaglandin E2 (PGE2), all of which are derived from activated CAFs and act through paracrine signaling on the non-small cell lung cancer (NSCLC) cells, prostate cancer cells, and intestinal cancer cells respectively (Geary et al., 2014; Guo et al., 2017; Roulis et al., 2020). Moreover, exosomal miRNAs such as miR-378c, miR-143, and miR-21, derived from CAFs, play significant roles in EMT and the generation of stem-like cells (Donnarumma et al., 2017; Yang et al., 2017).

All these data allude to the critical role of the CAFs, being an intermediary, following commands from tumor cells to stimulate stemness. Nonetheless limited data in this domain necessitates further efforts to fill knowledge gaps.

The ability of CAFs to induce cancer invasion and metastasis is their most significant distinguishing attribute compared to NFs. Data suggests that CAFs remodel the ECM, leading to cancer progression through invasion and metastasis (Dumont et al., 2013b). Answering the controversy regarding whether the number of CAFs decreases or increases to cause the cancer cells to invade ECM, an exciting study employing a deep learning cell identification algorithm using TCGA suggested an increase in the number of CAFs in the TME (Shapcott et al., 2019). The CAF model differs from typically observed cancer cell metastasis in invadopodia-independent and MMP-independent matrix degradation processes (Cao et al., 2016; Glentis et al., 2017). The heterogeneity and plasticity of CAFs are also critical for invasion and metastasis. The interplay among the microbiota present in the TME portrays itself as the cat’s-paw for the metastatic cells. We have learned about two distinct CAFs, differentiated in terms of heterogeneity of surface markers (CD146^+/−). CD146^- CAFs have been shown to enrich the TME with the production of proteins responsible for invasiveness, such as tenascin C (TNC), lysyl oxidase (LOX), and fibronectin 1 (FN1) (Brechbuhl et al., 2020). Earlier studies showed that CD146⁺ cells may represent a more mature pericyte subpopulation than CD146^- cells (Hassanpour et al., 2020; Manocha et al., 2022). CD146^- is a potent marker for risk analysis for lymph node metastasis, and patients with higher CD146^- cells have a poor prognosis (Brechbuhl et al., 2020). In convergence, the accumulated fibronectin (FN) in CAFs accelerates the invasion mainly via integrin-αvβ3. The assembled FN and the expression of αv and β3 integrins are directly proportional to the capacity to breach the basement membrane (BM) (Attieh et al., 2017). However, another integrin α₁₁β₁, a stromal cell-specific receptor for fibrillar collagens, indirectly aids in lung metastasis via facilitating trans-differentiation of CAFs (Navab et al., 2016).

It is broadly accepted that the tumor-promoting microenvironment in metastasis lesions emerges prior to the arrival of cancer cells, a process known as premetastatic niche (PMN) development (Fares et al., 2020). Soluble factors such as TGFβ, VEGF, and TNF, and EVs, like exosomes released by CAFs, promote PMN development. These factors then enter the circulatory system and spread to remote targets (Kong et al., 2019; Ping et al., 2021). Exosomes derived from CAFs contain non-coding RNAs (especially miRNAs) that regulate the cancer cells in a paracrine fashion (Yang et al., 2019; Li et al., 2021; Zhan et al., 2021). The differential distribution of these miRNAs in CAFs and NFs draws a thin line between their ability to manipulate the cancer cells to grow and invade distant tissues (Herrera et al., 2018). For example, miR-92a-3p expression was dramatically elevated in colorectal cancer (CRC) cells following phagocytosis of CAFs-derived exosomes (Hu et al., 2019). Again, a decrease in the miR-3188 levels in the CAFs-derived exosomes compared to that of NFs has been stated to have a role in turning on malignant phenotype in head and neck cancer cells (Wang et al., 2019).

POSTN ⁺ CAFs have been demonstrated to enhance lymph node metastasis as well as boost cancer cell proliferation and invasiveness (Hong et al., 2010; Wei et al., 2021). They activated the integrin-FAK/Src-VE-cadherin signaling cascade to penetrate lymphatic endothelial barriers, culminating in metastatic dissemination (Hong et al., 2010). CAFs are also reported to facilitate metastasis depending upon the presence or absence of stanniocalcin-1 (STC1). Pena et al. (2013) (Pena et al., 2013) demonstrated that CRC cells failed to invade and migrate in vitro and in vivo when co-cultured with STC1-deficient CAFs and grown in an orthotopic mouse model, respectively (Pena et al., 2013).

The predominant stromal cells in the TME account for the primary ECM source and thus can easily be attributed to its novel ability to modulate the same. Glentis et al. (2017) demonstrated a crucial role of CAF-containing stroma in paving the matrix-metalloproteinases (MMP)- independent mechanism of invasion by the colon cancer cells (Glentis et al., 2017), in contrast with previous belief that MMP2 and -9 are pre-requisites for metastatic dissemination of cancer cells to distant locations (Taguchi et al., 2014). The activation of CAFs and expression of αSMA rest on the secretome of CAFs. According to Tang et al. (2016), the invasive tendency of breast cancer cells grown in vitro is caused by the downregulation of the miR-200s (miR-200 family), which is consistent with the prometastatic nature of CAFs. These studies also shed insight into the functions of miRNAs in the transdifferentiation of fibroblasts (Tang et al., 2016).

Although molecular aberrations prevail in cancer cells, however, epigenetic alterations and variable miRNA expression are mostly fundamental for the cancer-promoting properties of CAFs. Despite several early reports of p53 mutations in the stromal compartment, it is now widely believed that CAFs do not carry p53 mutations (Hu et al., 2005; Fukino et al., 2007; Bechtel et al., 2010; Zhao et al., 2012). However, an oncogenic gain-of-function is attained inside cancer cells, above and beyond ablating the tumor suppressive function, upon mutation in the TP53 gene (Muller and Vousden, 2013). At the early stage of carcinogenesis, p53 functions as a cell non-autonomous tumor suppressor in the fibroblasts, in part by preventing the production and secretion of several molecules that might promote tumor growth (Kiaris et al., 2005; Moskovits et al., 2006; Addadi et al., 2010; Otomo et al., 2014). However, sustained cross-talk with the cancer cells induces trans-differentiation of their neighboring fibroblasts into CAFs (Kalluri, 2016). In agreement, Arandkar et al. (2018) have demonstrated the role of CAFs in invasion and metastasis correlating to an altered p53 function in the CAFs, suggesting that p53 acted as an essential modulator of the epigenetic machinery of CAFs in comparison with NFs. p53 was shown to have inherent, cell-autonomous, and unique characteristics imparted upon CAFs compared to NFs. A global transcriptome analysis using RNA sequencing data showed that 1,662 genes were expressed differentially in CAFs, supporting cancerous growth, proliferation, invasion, and migration. Cancer cells’ migratory characteristics were attenuated on silencing p53 in the CAFs (Arandkar et al., 2018).

New vasculature connectivity formation is essential because tumor cell proliferation and metastatic spread rely on optimal oxygen intake, supply of nutrients, and waste elimination (Lugano et al., 2020; Notohamiprodjo et al., 2021). The endogenous angiogenic factors responsible for the activation of neovasculature are namely VEGF, bFGF, TGFα, TGFβ, TNFα, angiogenin, PDGF, G-CSF, placental growth factor, IL-8, HGF, and epidermal growth factor (EGF) (Nishida et al., 2006). The role of CAFs in neovasculature to aid hypoxic tumor cells depends broadly on the positive and reciprocal feedback among CAFs and tumor cells. CAFs recruit endothelial cells and stimulate vascularization, triggering angiogenesis for the nutrient supply to cancer cells (Sewell-Loftin et al., 2017). The connective tissue growth factor (CTGF) expression is essential for boosting microvessel density and attracting endothelial cells in experimental xenograft models of CAF-mediated angiogenesis through the expression of SDF-1/CXCL12 (Denton et al., 2018). Apart from that, there is another indirect role of CAFs in triggering angiogenesis. As discussed, CAFs regulate and modify the ECM in favor of the cancer cells to grow and metastasize. Such modifications include the upregulation of MMP9 and MMP13, leading to the secretion of pro-angiogenic growth factors like VEGF (Boire et al., 2005; Vosseler et al., 2009).

Overexpression of SDF-1/CXCL12 by αSMA ⁺ CAFs and simultaneous downregulation of mDia2 protein triggered pro-angiogenic secretome profile in breast cancer (Orimo et al., 2005; Yu et al., 2014; Dvorak et al., 2018). Apart from secreting VEGF, CAFs recruit endothelial progenitor cells (EPCs) in the breast cancer TME resulting in angiogenesis (Orimo et al., 2005; De Francesco et al., 2013). In line, Wang et al. (2014a) showed malignancy and angiogenesis in nasopharyngeal carcinoma (NPC) in a VEGF/CXCL12-CXCR4 dependent manner, and the presence of EPCs was also confirmed with CD133 ⁺ cells in the tumor stroma. Two independent research groups reported that the SDF-1/CXCR4 cascade was also employed by αSMA⁺ CAFs following HIF-1α mediated conversion into CAFs from NFs (Zagzag et al., 2005; Errarte et al., 2020). Recent research unveiled an exciting correlation of αSMA and CD90 of CAFs with neighboring HCC tissue expression of placental growth factor (PGF) (Liu et al., 2020a). PGF causes blunted anti-tumor immunity by M2 polarization and creates a pro-angiogenic environment by triggering the inflammatory markers, NF-κB and COX2 in CAFs (Albonici et al., 2019). With the help of TCGA analysis, Liu et al. (2020a) showed that the co-expression of PGF and CD90 in the tumor milieu could be directly correlated to the angiogenesis markers CD31, CD34, and CD105 leading to poor prognosis of HCC patients.

In a study by Erez et al., 2010, PDGFRα ⁺ CAFs were sorted from a squamous cell carcinoma tumor milieu (SCC) to decipher the role of inflammatory secretome and others in triggering pro-angiogenic signal transduction. Two different pathways could be decoded to reach VEGF expression: directly through OPN and CYR61 expression or secondarily via the expression of inflammatory genes CXCL1/2/5 (Erez et al., 2010).

CAF-secreted exosomes containing miRNAs play a significant part in angiogenesis too. miR-21 was widely accepted to induce VEGF-mediated pro-angiogenic signaling in an autocrine fashion (Asangani et al., 2008; Wu et al., 2017). Nevertheless, the CAF-exosomal miR-21 might also add to the cumulative induction in a paracrine style (Yang et al., 2017). Ten-eleven translocation 2 (TET2) was found to be the target of cancer cell-secreted miR-210 in CAFs, which has been implicated in the pro-angiogenic switch. A recent analysis revealed that miR-210 had the capacity to elevate the expression of some pro-angiogenic factors, including MMP9, FGF2, and VEGFa, in CAFs, by activating the JAK2/STAT3 signaling pathway (Fan et al., 2020). Furthermore, miR-135b-5p upregulation in the CAF-derived exosomes supported the CRC cell migration and angiogenesis (Yin et al., 2021).

The English surgeon Stephen Paget (1855-1926) postulated the “seed and soil” theory a century ago to describe the role of tumor stroma in the growth and dissemination of cancerous cells. The “seed” is the cancer cell, while the stroma or the microenvironment is considered the “soil” for the “seed” (Paget, 1889; Ribatti et al., 2006). Current knowledge suggests that the soil requires positive reciprocal feedback from the seed or that it sometimes needs to be educated about the needs of the seed. For example, we may consider one of the many different means discussed that resulted in a transdifferentiation mesenchymal to mesenchymal transition (MMT) of NFs to CAFs (Sahai et al., 2020a; Ping et al., 2021). p53 non-autonomous expression pattern in the CAFs is believed to be due to the education imparted by the cancer cells. Furthermore, qRT-PCR further confirmed that MMP1, MMP3, and MMP10 mRNA were upregulated in CAFs in a largely p53-dependent manner, precisely opposite to NFs (Arandkar et al., 2018).

CAFs are considered the key ECM modulator in the tumor stroma, influencing tumor development, intravasation, migration, extravasation, and metastasis (Sahai et al., 2020a). Many malignancies are characterized by increased collagen synthesis (Liu et al., 2019a). Increased collagen synthesis and cross-linking, in particular, are linked to increased tumor stiffness and advancement (Xu et al., 2019). A cancer spheroid formation model of ovarian cancer confirmed the role of CAFs in influencing collagen type I, particularly by expressing versican, which promoted cancer invasiveness via the TGFβ pathway (Yeung et al., 2013). In addition, CAF-derived laminin was shown to interact with integrin α₆β₄ to trigger the migration of cervical cancer cells (Fullar et al., 2015). Following conversion into CAFs, contractile capabilities increase as αSMA and vimentin expression levels rise. That gives rise to its morphological modification by giving it a stellate shape (Kalluri, 2016), and several different soluble and insoluble secretions, including ECM proteins, are observed to be significantly intensified. Fibronectin is deposited first by the CAFs, which produces and intensifies intracellular tensions via increased interaction with actin filaments. In the case of wound healing, a positive feedback loop keeps the fibroblasts activated, and the translocation of yes-associated protein (YAP) into the nucleus triggers overexpression of αSMA (Kollmannsberger et al., 2018). Before producing and conducting tensile strength to the matrix to remodel it, the contractility of the CAFs needs to get amplified. That occurs through the activation of the Rho-ROCK-Myosin II signaling cascade by the signals from newly synthesized ECM and subsequent amalgamation of αSMA with actin-myosin fibers (Gaggioli et al., 2007; Provenzano and Keely, 2011). The CAFs modify the composition by modulating the amount and expression of MMPs, and mechanically, they change the physical properties of the ECM by modifying its organization and stiffness (Jang and Beningo, 2019).

Participation of additional fibroblasts generates a negative feedback loop to reduce the fibronectin/collagen I ratio leading to the relaxation of fibronectin fibers and CAFs entering quiescence. In contrast to the physiological context, fibronectin fibers are not let relaxed to resume quiescence; instead, the fibronectin zones are altered as a preventive measure against relaxation, which, in turn, leads to continuous ECM remodeling in the tumor context (Cox and Erler, 2011; Pickup et al., 2014; Leight et al., 2017; Barbazán and Matic Vignjevic, 2019). These secretions allow the CAFs to stay activated and communicate with the neighboring cells, such as endothelial cells and immune cells, in the stroma. Several trials targeting the alliance between CAFs and ECM modifications in recent years have unraveled that it not only supports the cancer progression, but the efficiency of targeting also depends on the tissue and carcinogenesis stage-specific context (Amakye et al., 2013; Van Cutsem et al., 2020). In some cases (e.g., breast, colon, pancreatic, stomach cancer), the stromal fraction of solid tumors can vary widely, amounting to 60%–90% of the overall tumor mass (Ronnov-Jessen et al., 1996; Dvorak, 1986; Powell et al., 2005; D'Arcangelo et al., 2020). In fact, TME can be very much influenced by the CAFs through the formation of severe desmoplastic reactions creating a desmoplastic TME (Liu et al., 2019a; Zeltz et al., 2020b). Cancer dissemination from PDAC to other organs can be attributed to desmoplasia (Shimosato et al., 1980; Halvorsen and Seim, 1989a; Halvorsen and Seim, 1989b; Hasebe et al., 2002; Iacobuzio-Donahue et al., 2002; Koliopanos et al., 2002; Caporale et al., 2005). However, in the case of CRC, the role of desmoplasia is not as straightforward as PDAC (Hewitt et al., 1993).

In a previous study by Erkan et al., 2008, increased stromal activity (but not stromal density) and diminished collagen deposition were correlated with a worse prognosis. In contrast, lower stromal activity (indicated by low αSMA expression) and increased collagen deposition were synchronized with a better prognosis (Erkan et al., 2008). This came with a contradiction against the dogma that collagen-induced signals highly favor the aggressiveness of cancerous growth (Whatcott et al., 2015; Insua-Rodríguez and Oskarsson, 2016). In another study, Bever et al. (2015) (Bever et al., 2015) illustrated the correlation between stroma density and patient survival and stroma activity using a computer-aided quantitative method in a cohort of 66 PDAC patients under adjuvant medication following a pancreaticoduodenectomy. In line with this, Chen et al. (2021) demonstrated that deletion of type 1 collagen in αSMA⁺ myofibroblasts exaggerated PDAC, probably due to high stromal activity. More studies in the field of collagen arrangements in the stroma found that rather than the collagen quantity (presence or absence of collagen), it is the collagen quality (thickness and alignment) that is indicative of poor disease prognosis (Drifka et al., 2016; Laklai et al., 2016). That concludes that activation of CAFs and ECM modification is equally essential for cancer progression and metastasis.

The ECM stiffness gives rise to invadopodia formation from actomyosin beams in cancer cells. The rate of invadopodia formation and matrix degradation depends upon the contractility of actomyosin beams (Aung et al., 2014; Jerrell and Parekh, 2014). The invadopodia are enriched with MMPs that form passages for the cancer cells to infiltrate into the ECM by degrading the same (Kessenbrock et al., 2010; Schoumacher et al., 2010). However, recent research reported that CAFs could degrade the ECM in a manner independent of invadopodia. It utilizes the tubular organization, employing MT1-MMP (MMP-14) or MMP-2 protein to remodel the matrix in favor of tumor cell invasion and metastasis (Cao et al., 2016). SPARC, secreted from CAFs, supports the pro-tumor mechanisms in many cancer types. Through the differential nature of executions in a few cancer types, it aids cell invasion by enhancing MMP expression by CAFs as well as by monocytes (Tremble et al., 1993; Neuzillet et al., 2013).

CAFs, educated via TNFα and NF-κB pathway by the p53 mutant cancer cells, in the stroma of metastases have been shown to release significantly high quantities of perlecan in order to attract cancer cells (Pereira et al., 2019). Thus, the cancer cells, CAFs, and immune cells secrete large amounts of VEGF, PDGF, and FGF-β which add to the basement membrane’s (BM) pre-stored growth factors and are finally released after degradation by the MMPS (Kalluri, 2003). The disorders created in the BM enhance tumor cell invasion by helping pro-angiogenic mechanisms.

Moreover, CAFs may indirectly influence inflammatory cell recruitment as well as functioning via ECM deposition and matrix remodeling (Rubin et al., 1995). CAF-directed ECM alteration is important for monocyte and other myeloid cell recruitment. The stiffness of the ECM supports the release of chemoattractants like CCL2 and colony-stimulating factor-1 (CSF-1) from CAFs and tumor cells (Acerbi et al., 2015; Nielsen et al., 2016). The composition, density, and organization of ECM support the passage of immune cells through the stroma. While hyaluronan and fibronectin prevailing stroma can promote T-cell migration through ECM, versican and tenascin can inhibit the same (Loike et al., 2001; Evanko et al., 2012; O'Connor et al., 2012; Bollyky et al., 2011; He and Baum, 2004). On the other hand, the pro-tumorous M2 macrophages can be recruited and blocked by collagen and hyaluronan-rich and SPARC-rich matrices, respectively (Kuang et al., 2007; Kobayashi et al., 2010; Sorokin, 2010; Iijima et al., 2011).

CAFs and immune cells are the most prevailing cell types within the tumor stroma. Among the immune cells, CAF-derived secretome affects many leukocytes, including CD8⁺ T-cells, T_reg cells, and the most abundantly present macrophages (Figure 3). Considering their vast role in TME in tumor progression, invasion, metastasis, and acquired resistance to therapy, the macrophages (henceforth will be designated as ‘tumor-associated macrophages’ or TAMs) will cover a big part of our discussion.

Besides TAMs, CAFs have a multifaceted level of interactions with natural killer (NK) cells, dendritic cells (DC), T lymphocytes, myeloid-derived suppressor cells (MDSCs), and tumor-associated neutrophils (TANs), forming a complex tumor-immune interface (An et al., 2020). As discussed in previous sections, the putative impact of the CAF-derived secretome affects immunosurveillance negatively. Exceptions include the interaction of DC cells from hepatocellular carcinoma (HCC), bone marrow cells, and CAFs in a co-culture system generating IL-1β, IL-6, and IL-12p70, which subsequently activates cytotoxic T lymphocytes (T_C cells) to release interferon (IFN-) α, and IFN-γ, eliciting an anti-tumor effect (Qian et al., 2018). The interactions with other cells have been discussed in-depth in previous sections detailing the functions and diversity of CAFs (Fearon, 2014; Lakins et al., 2018a; Costa et al., 2018; Elyada et al., 2019). Zhang et al. (2019) have shown that CRC-derived CAFs could upregulate the expression of VCAM1 and secretion of IL-8, thereby recruiting and polarizing macrophages into the M2 phenotype, culminating in diminished NK cell function. Synergism between CAFs and TAMs in crafting an immunosuppressed TME was shown to regulate tumor-infiltrated NK cells (Zhang et al., 2019). Next to NK cells, Cheng et al. (2018) reported a novel mechanism regarding the effect of CAFs on tumor-associated neutrophils (TANs). IL-6 secreted from the CAFs induces STAT3/PD-L1 signaling pathway in TANs triggering chemotaxis and anti-apoptosis mechanism triggering an increase in the number of neutrophils in the TME. A previous report indicated that an N1/N2 phenotypic transition is attributable in the TANs, where N1 is considered to have anti-tumor activity, and N2 is regarded to be associated with immunosuppression, and pro-tumor cellular activities, by DNA instability or by secretion of chemokines and cytokines (Masucci et al., 2019; Lau et al., 2022). The prevalence of the N2 phenotype correlates with poor patient prognosis (Masucci et al., 2019).

Some clues indicate a clear association of CAFs with the polarization of TAMs. CAF-derived secretome includes a plethora of soluble effector molecules, and current studies indicate that CAFs are the regulators of different cell-mediated immune responses (Monteran and Erez, 2019b). In agreement with this, CAFs were able to recruit and differentiate macrophages into TAMs (Ziani et al., 2018; Hegab et al., 2019). CAFs are involved in MCP-1-mediated macrophage infiltration in skin tumors, nourishing chronic inflammation (Zhang et al., 2011). Likewise, podoplanin⁺ CAFs could recruit and differentiate monocyte into CD204⁺ TAMs (Sakai et al., 2018). With the key monocyte chemotactic cytokines MCP-1 and SDF-1, the CAFs from invasive human breast cancer were able to transform monocytes into M2-type pro-tumoral macrophages, changing the myeloid lineage structurally as well as functionally (Gok Yavuz et al., 2019). Interestingly, the newly transformed M2-type macrophages (TAMs) can activate CAFs in a positive feedback loop and promote cancer progression (Ueshima et al., 2019). The ephemeral reciprocation in the action of CAFs and TAMs was justified by Hashimoto et al. (2016), where the group demonstrated the advent of CAFs from bone marrow-derived MSCs, their role in increased invasiveness of TAMs, finally culminating in the generation and invasion of more CAFs (Hashimoto et al., 2016; Zheng et al., 2017). In addition to SDF-1, CAFs secrete CXCL14 in prostate cancer, which accelerates the recruitment of monocytes and further leads to their polarization into M2 TAMs (Augsten et al., 2014; Comito et al., 2014). Another mechanism of M2-phenotypic conversion was demonstrated in CRC, in vitro, where CAFs-derived IL-6 and IL-8 were found responsible for the conversion (Kim et al., 2012). ER^-/PR^-/HER2^- triple-negative breast cancer stroma-derived CAFs secrete CXCL16 that attracts monocytes and aids their stromal activation (Allaoui et al., 2016). Adenosine secretion by CAFs warrants great potential for monocyte differentiation and polarization into the M2 phenotype (Regateiro et al., 2012; Della Latta et al., 2013; Allard et al., 2016; de Leve et al., 2019). To describe the TME state that supports the recruitment and conversion of macrophages, Nakamura et al. (2018) deciphered that a hypoxic environment, substantiated by the marker carbonic anhydrase IX, contains both podoplanin⁺ CAFs as well as CD204⁺ TAMs (Nakamura et al., 2018). CD204⁺ TAMs are associated with immune suppression. Evidence-based data support the involvement of FAP⁺ cells in activating inflammatory STAT3 cascade via the uPAR-FAK-c-Src-JAK2 pathway. Myeloid-derived suppressor cells (MDSCs) are recruited to the tumor stroma to promote immunosuppression. CCL2, derived from FAP⁺ CAFs, is considered responsible for the CCR2-dependent immunosuppression by the MDSCs (Yang et al., 2016a; Kumar et al., 2017). CD163⁺ TAMs infiltrated the tumor stroma in triple-negative breast cancer and nasopharyngeal cancers, indicating a close association between CAFs and TAMs (Yu et al., 2018b; Zhou et al., 2018). In addition to direct mechanisms involved in M2 polarization by CAFs, there lies an indirect path as well. The pancreatic stellate cells (PSCs), considered the critical source cells of CAFs in PDAC, could stimulate IL-13-secreting mast-cells, promoting M2 macrophage polarization (Ma et al., 2013; Varricchi et al., 2017).

The crosstalk between CAFs and TAMs (M2-type), along with other cells, and their positive and reciprocating aid towards pro-tumorous, immunosuppressed TME greatly facilitated tumor growth and immune evasion (Hashimoto et al., 2016; Gunaydin, 2021). Further, the CAF-TAM communication was also helpful in advancing cancer with angiogenesis and metastasis (Comito et al., 2014; Doak et al., 2018). CAF/TAM milieu is associated with the generation of perlecan-rich desmoplastic stroma at metastatic sites (Brasil Da Costa et al., 2020). To aid metastasis, CAFs recruit EPCs (Orimo et al., 2005; De Francesco et al., 2013; Wang et al., 2014a) that aid in bringing in epigenetic modifications in the cancer cells in collaboration with the CAFs. The modification leads to a mesenchymal-to-amoeboid transition (MAT), helping in the metastatic spread of tumor cells (Giannoni et al., 2013). Linde et al. (2018) illustrated the role of CAF-educated TAMs (CD206⁺) in metastasis. The CD206⁺ M2 macrophages were able to downregulate the E-cadherin in breast cancer cells, promoting EMT (Linde et al., 2018). Moreover, CAFs-secreted IL-33 triggered the M2 TAMs to upregulate the MMP-9 expression, enabling ECM modification (Andersson et al., 2018). There is substantiating evidence indicating the ability of CAFs to induce EMT, invasion, and metastasis (Karagiannis et al., 2012).

Stepping into the roles of CAFs in immune evasion, the primary conception leads us to infer that the M2 phenotypic milieu in the TME is key to immune evasion for the tumor cells. Moreover, CAF-derived secretome includes TGFβ, IL-10, and arginase I to add to the immunosuppressive profile (Takahashi et al., 2017). By secreting adenosine, an immunosuppressive metabolite, the CAFs enhance immunosuppression and myeloid differentiation, proliferation, and invasion (Leone and Emens, 2018). Moreover, the synergism of CAFs and TAMs can hinder adaptive immunity by interrupting antigen presentation. Besides TGFβ and IL-6, CAF-secretome includes tryptophan 2,3-dioxygenase (TDO2), indoleamine-2,3-dioxygenase (IDO), and VEGF that can block DC maturation, a critical antigen-presenting cell (APC). The absence of proper antigen presentation calls for T-cell anergy, a crucial event disrupting the cell-mediated immune response (Gabrilovich et al., 1996; Dikov et al., 2005; Kitamura et al., 2005; Flavell et al., 2010; Kitamura et al., 2017; Ziani et al., 2018; Liu et al., 2019a).

Therefore, the orchestration between the primary stromal cells in association with CAFs promotes the tumor cell via immune evasion and immunosuppression to boost the pro-tumorous TME for enhanced proliferation, growth, invasion, and metastasis of distant tissues, which ultimately leads to disease progression.

Metabolism and metabolic crosstalk are indispensable parts of cancer. The secreted amino acids and other metabolites build a dialogue between the tumor cells and the stromal cells (Kay and Zanivan, 2021). Little is known about these interactions, and it remains open to answering how the CAF metabolism should be targeted for better patient prognosis.

Previous data suggest that CAFs show a characteristic hyper rate of glycolysis, and a proportional rate of autophagy is also typical. This event results in the release of a large amount of lactate, amino acids, and ketone bodies, which are subsequently taken up by tumor cells, helping them grow at a higher rate. The symbiotic dialogue between CAFs and tumor cells is the initial evidence of metabolic crosstalk (Pavlides et al., 2009; Whitaker-Menezes et al., 2011; Guido et al., 2012; Sousa et al., 2016). Aside from lactate, recent reports indicate pyruvate to be the major contribution of CAFs to the metabolome of the stroma as well. Significantly high secretion from breast CAFs and PDAC-CAF conditioned media substantiated the claim for a pyruvate-rich metabolome (Becker et al., 2020; Kerk et al., 2020). Kerk et al. (2020) described that the CAF-secreted extracellular pyruvate maintained redox homeostasis and was beneficial in developing resistance against mitochondrial inhibitors in pancreatic cancer. Strategic aid from pyruvate was again validated by the reports of lymphoma cell survival and ECM remodeling by metastatic breast cancer cells (Sakamoto et al., 2019).

In the case of pancreatic cancer, the quiescent stellate cells get converted into activated fibroblasts (CAFs) and release the stored lipid to assist as a signaling molecule for biomass production. For example, lysophosphatidic acid released from CAFs activates the PI3K/Akt signaling cascade in favor of cancer cell proliferation (Auciello et al., 2019).

The activity of cancer cells-derived-TGFβ and oxidative stress in rewiring CAF metabolism, inspiring glycolysis, and autophagy is widely accepted (Martinez-Outschoorn et al., 2010; Guido et al., 2012). The TGFβ assists the branched-chain keto acid production in CAFs. Branched-chain keto acids are used by cancer cells as carbon and nitrogen sources and were also deciphered from the overexpression of branched-chain amino-acid aminotransferase (BCAT) 1 (Zhu et al., 2020). Autophagy-derived alanine from CAFs is, reportedly, taken up by the PDAC cells to aid the TCA cycle, where the initial starting molecule is derived from pyruvate (Sousa et al., 2016; Auciello et al., 2019; Sanford-Crane et al., 2019). So metabolic convergence between the different sources can be met to justify the proliferation and growth of cancer cells.

Breast cancer-derived exosomes could activate the proto-oncogene MYC in the stromal fibroblasts in a positive and reciprocal feedback loop, as the activated CAFs then secret exosomal factors to be taken up by the cancer cells. This results in cancer cell proliferation via an increase in glucose and glutathione metabolism (Zhao et al., 2016; Yan et al., 2018b). Other metabolic exchanges include glutamine-glutamate exchange that benefits both CAFs and cancer cells. Inhibition in the synthesis of glutamate or glutamine showed reduced tumor growth (Yang et al., 2016c). As mentioned before, if not starvation, nutrient deficiency is a common condition for cancer cells. CAFs have been reported to support prostate cancer cells under glutamine deficiency in an ATF4-dependent manner via pyruvate carboxylase-asparagine synthase overexpression (Linares et al., 2017), where stromal asparagine was used as an alternative source of nitrogen. In stiff ECM, CAFs enhance their rate of glycolysis and oxidative phosphorylation. At this stage, CAF-derived aspartate is taken up by cancer cells, and in convergence, cancer cells-derived glutamate is taken up by the CAFs. Interestingly, this feedback loop stimulating cancer cell growth and invasion offers a common target glutaminase-1 (GLS1) to neutralize both pathways (Bertero et al., 2019).

For CAFs, creating a hypoxic environment is key to nurturing and expediting the growth of cancer cells with more glycolytic enzymes in the stroma. In addition, CAF autophagy also nurtures the metabolic needs of the proliferating cells by delivering lactate and other metabolites (Martinez-Outschoorn et al., 2010; Zhang et al., 2015). An entire epigenetic shift is responsible for adopting the pro-tumorigenic qualities of the TME. It is believed that hypoxia leads to a pro-tumorous gain of characters that include changes in gene expression patterns of CAF markers and ECM components via NNMT (Nicotinamide N-methyltransferase) mediated hypomethylation. Such changes were reported in ovarian CAFs (Eckert et al., 2019). Breast CAFs also supported a similar paradigm by acquiring hypomethylation of promoters of genes responsible for glycolytic enzyme synthesis (Becker et al., 2020). An upregulated NNMT in ovarian, colorectal, and gastric cancers indicates an active role of the enzymes in hypoxia-related hypomethylation (Eckert et al., 2019; Song et al., 2020; Zhang et al., 2021). These suggest that an epigenetic shift occurred, altering the CAFs to be pro-tumorous and remain active even in the absence of the primary inducer.

The function that gets affected by the altered metabolism of CAFs is the immune response against the tumor cells. Netrin G1 (NTNG1) is known for its role in glutamate and glutamine synthesis by CAFs, which is further taken up by cancer cells to expedite their energy needs. NTNG1 is also associated with immunosuppressive cytokine synthesis by CAFs (Kay and Zanivan, 2021). Therefore, the metabolism of CAFs has a multifaceted role inside the stroma, including nutrient supply to cancer cells and pro-tumorigenic immunomodulation.

The main categories of overall chemoresistance induced by CAFs include ECM remodeling, paracrine signaling, induction of stem-like properties in cancer cells, metabolic manipulation, modulation of the immune environment in the TME, and exosomal shuttling between tumor cells and CAFs.

CAF-induced chemotherapy resistance involves multifaceted processes that generate a physical barrier by modifying the extracellular matrix (ECM). This barrier reduces drug accessibility to tumor cells, activates pro-survival signaling pathways, and inhibits apoptotic signaling pathways. ECM remodeling by CAFs may also result in increased EMT and stem-like properties, aggressive cancer cell transitions, epigenetic modulation, and general modulation of the crosstalk between breast tumor cells and stromal components in the TME (Maji et al., 2018). CAFs secrete type 1 collagen, which inhibits chemotherapeutic drug absorption in solid tumors (Luo et al., 2015).

Studies in vitro indicate that stromal-derived paracrine signaling can increase cancer cell survival following chemotherapy (Valkenburg et al., 2018). Chemotherapy-induced DNA damage in CAFs has been observed to increase the expression of various inflammatory, angiogenic, or EMT-inducing signals (HGF) (Vickman et al., 2020). There are cases of chemotherapeutic drugs activating NFs and promoting tumorigenic CAFs that are involved in paracrine signaling. For example, Hedgehog-GLI signaling induces stemness in cancer cells which can result in chemoresistance (Peiris-Pagès et al., 2015). CAF-mediated TGFβ signaling, along with other pro-EMT and tumor-promoting signaling pathways, causes breast tumor cells to resist chemotherapy and become more aggressive. Studies identifying pro-tumorigenic CAF subpopulations have contributed to expanding our scope of identifying paracrine signaling molecules and pathways. Han et al. (2021) investigated the molecular mechanism of paclitaxel resistance, a chemotherapeutic drug, in TNBC and correlated chemotherapy resistance in TNBC PDX models to JAK2 signaling and an enriched cCAF subpopulation (Han et al., 2021a).

The induction of stemness in cancer cells has been a crucial aspect of therapy resistance in all types of cancer. After treatment, the risk of repopulation and relapse is due to the ability of stem-like cancer cells to resist anti-cancer therapies. The evidence that CAFs are also a cause of inducing CSC populations in tumors is essential for comprehending the methodologies of chemotherapy resistance and preventing relapse. Su et al. (2018) demonstrated that the cell membrane proteins CD10⁺ and GPR77⁺ are responsible for the maintenance of stemness in breast CSC populations (Su et al., 2018). These populations are positively correlated with the expression of CD10⁺ GPR77⁺ CAFs, revealing that this subset of CAFs maintains stemness through TME modulation (Su et al., 2018).

Yu et al. (2017) described a stromal GPER-mediated drug resistance and increased mitochondrial activity in the reprogramming of breast cancer energy metabolism. The stromal environment is particularly acidic, but the relationship between lower pH and CAF-secreted lactate can also be associated with chemoresistance through metabolic reprogramming (Tavares-Valente et al., 2013). In agreement with this, the upregulation of Ras signaling in CAFs correlates with an increase in glutamine synthesis, which supports the mitochondrial metabolism of cancer cells and renders them more resistant to chemotherapy, particularly drugs that inhibit androgen signaling (Mishra et al., 2018). Understanding the mechanisms by which CAF influences the metabolism of tumor cells is a promising strategy for addressing issues of therapy resistance and cancer severity.

NFs play an integral role in immune response, and CAFs exploit this function to facilitate cancer cell immune evasion. NK cell abrogation is achieved by exposure to CAF-derived TGFβ through miR-183 mediated DAP12 transcription interruption, thus resisting chemotherapy and aiding cancer cell survival (Powell and Huttenlocher, 2016). The secretion of soluble factors has extensive effects on the EMT, proliferation, migration, and stem-like properties of cancer cells, as well as a prominent influence on immune response and evasion. CXCL secreted by CAFs recruits TAMs, stimulating cancer progression and chemoresistance (Shien et al., 2017). Due to its immunomodulating effects, the clinicopathological significance of CAF PD-L1 expression in TNBC has been identified as a reliable predictor of treatment response and prognosis (Yoshikawa et al., 2021). Interferons, which play a crucial role in immunomodulatory functions, are modulated by CAFs resulting in therapy resistance and tumor progression. Activation of IFN signaling induced by CAFs in claudin-low TNBCs resulted in chemotherapy resistance, as demonstrated by Broad et al. (2021) (Broad et al., 2021). Targeting IFN receptors and other signaling axes involved in CAF-dependent chemoprotection via immunomodulatory functions makes it possible to find more efficacious means of enhancing treatment outcomes. CAF-derived chemokines such as IL-8 or CXCL8 recruit immunosuppressive cells to the TME, consequently enabling effective tumor progression, angiogenesis, and EMT (Han et al., 2021b). Promoting immunosuppression by CAFs in the TME can result in resistance to chemotherapy and other therapies (Hu et al., 2021). CAFs also affect the ratio of immune cells within the TME, notably by increasing the proportion of FOXP3⁺ T-cell T_reg to CD8⁺ T lymphocytes, which leads to poor treatment outcomes and a diminished antitumor immune response (Mhaidly and Mechta-Grigoriou, 2021). The mechanisms of CAF immunomodulatory pathways may be crucial to our comprehension of CAF-influenced chemotherapy resistance.

Cancer cells have been seen to have gemcitabine and paclitaxel resistance in pancreatic cancer due to an association between CAFs, TAMs, and stromal-derived insulin-like growth factors (Ireland et al., 2016). Conversely, breast cancer cells increased chemotherapy efficacy by blocking the insulin-like growth factors from stromal components (Ireland et al., 2018). A possible counter to this is to target GPR77 membrane proteins in CAFs to promote chemosensitivity and reduce CSC count (Su et al., 2018). It has also been found that in vitro VCAM-1 knockdown in breast cancer cells reduces the proliferation and migration of IL-6-influenced breast cancer cells, thus increasing chemosensitivity (Wang et al., 2014b). Other methods of countering chemoresistance, such as aspirin treatment, have been reported to be effective as well, although their relationship to CAF-induced stemness still needs to be explored (Saha et al., 2016). More focus needs to be paid to how autophagy influences TME. To combat the chemoresistance brought on by CAFs, small compounds that target the autophagy-related core machinery may be a viable option. In a PDAC animal model, CAF depletion via disruption of the Hh signaling or injection of hyaluronan improved chemotherapy (gemcitabine) delivery (Olive et al., 2009). CAF-targeting strategies have shown progress in our understanding of how to increase chemotherapy efficacy and decrease overall tumor progression.

It has been well established that hormone imbalance, specifically endogenous estrogen and progesterone, can cause breast cancer via receptor-dependent and -independent mechanisms (Trabert et al., 2020). In addition to other secreting growth factors, cytokines, and proteases, estrogen can be secreted from CAFs and may be used to predict the efficacy of endocrine therapy and treatment response (Yu et al., 2017; Ruocco et al., 2018). Adjuvant endocrine therapy is an effective strategy against estrogen receptor-positive and other related types of breast cancer, such as luminal A, luminal B, or HER2⁺ (Schiavon and Smith, 2014; Burstein et al., 2019). In luminal breast cancer, microvesicle-mediated miRNA transfer transforms non-CSCs into CSCs that induce resistance to most therapies, including hormonal therapy. An example of this involves a study confirming the role of CAFs in the presence of hormone therapy resistance by modulating hormonal receptors or activating signaling pathways such as PI3K/AKT and MAPK/ERL1 and ERL2 signaling axis involved in tamoxifen resistance (Martinez-Outschoorn et al., 2011). Anti-estrogen resistance in breast cancer was found to be overcome by inhibiting mitochondrial function in breast cancer cells (Martinez-Outschoorn et al., 2011). Stromal factors influence the TME, and CAF-induced β1 integrin signaling promotes tamoxifen resistance in breast cancer (Pontiggia et al., 2012). Exosomal or vesicular transfer between tumor cells and CAF secretome frequently results in an active feed-forward loop involving CAFs and tumor cells that increases tumor-promoting CAF activation and aggressive features in cancer cells. Specifically, Cosentino et al. (2020) discovered that miR-9-mediated inhibition of EFEMP1 contributed to the upregulation of pro-tumor CAF phenotypes.

Developing methods to prevent the formation of CAF-influenced therapy-resistant tumor cells can increase the clinical efficacy of hormone therapy. Luque et al., 2021 showed that the CAFs, derived from HER2⁺ patients, promoted resistance to trastuzumab and pertuzumab treatment in vitro. However, the correlation with the presence and impact of CAF-S4 was not considered so far. The HER2-amplified breast cancer cells are resistant to tyrosine-kinase inhibitor lapatinib due to CAF manipulation of the ECM rigidity through YAP/TAZ activation (Lin et al., 2015). Soluble factors secreted by CAFs have been explained to cause tumor resistance to anti-HER2 therapies. CAF-derived FGF5 in breast cancer has caused resistance to HER2-targeted therapies through activation of the FGFR2 and c-Src downstream pathways (Fernández-Nogueira et al., 2020). Other secretory growth factors of interest including TGFβ and HGF regulate cancer-related pathways and tumor progression which can be tied to HER2 therapy resistance (Ikushima and Miyazono, 2010; Luraghi et al., 2014). Using a multi-omics approach to identify cytokines, transcription factors, kinases, and miRNAs or other secretory factors that CAFs release can aid in the identification of novel biomarkers that cause therapy resistance in HER2⁺ breast cancer and other forms of cancer.

CAFs can influence the radioresistance of cancer cells with simultaneous activation of alternative mechanisms for their proliferation and progression. Irradiated fibroblasts have been observed to overcome apoptotic signaling and transform into activated phenotypes that promote tumorigenesis (Ansems and Span, 2020). In a recent study, co-cultured CAFs and cancer cells developed resistance to the clastogenic effects of 137Cs gamma rays due to the enhanced capacity of CAFs to repair DNA damage (Domogauer et al., 2021). It is likely that the CAFs that survived radiation therapy modulated the fate of associated cancer cells and caused radiation resistance in the tumor as a whole. Exosomes derived from colon CAFs contribute to radioresistance by promoting cancer stem-like phenotypes (Liu et al., 2020b). With CAF-derived exosomes comes the consequent activation of tumor-promoting signaling pathways and stemness induction, instilling resistance in tumor cells (Liu et al., 2020b). Production of TGFβ by radio-treated CAFs can also promote cancer cell aggressive and invasive properties, acting as a radiotherapy therapeutic escape and resistance (Papadopoulou and Kletsas, 2011; Zhang et al., 2017). Notch signaling in CAFs plays a role in radioresistance, as demonstrated by a recent study that identified single-cell transcriptomic profiles in CAF subpopulations in delta-like canonical Notch ligand 1, Dll1⁺ tumors (Nandi et al., 2022). The connection between Notch signaling and CAF-associated metastasis and radioresistance could be exploited to improve breast cancer patient outcomes by minimizing radioresistance and stemness (Nandi et al., 2022). The increased expression of CXCL12, TGFβ, MMPs, and HGF in CAFs induced by radiation increases the activation of EMT pathways in cancer cells (Ansems and Span, 2020). In the majority of radiotherapies, similar mechanisms involving CAF-derived ECM remodeling and desmoplasia, hypoxia-induced TME, autophagy-induced cancer cell recovery, secretory factors, exosomes, and miRNA cause downstream signaling of cyclization and tumor resistance (Mantoni et al., 2011; Horsman and Overgaard, 2016; Wang et al., 2017). Radiotherapy-induced immunomodulatory mechanisms include CAFs avoiding immune recognition and retaining immunosuppressive properties within the TME (Song et al., 2021). Overall, radiotherapy resistance observed in cancer cells has been linked to CAF activity in the tumor microenvironment; therefore, comprehensive studies on the effects of CAFs on radioresistance can lead to an increase in overall survival and the potential development of successful combination therapies.

Recent research has shown that CAFs play a significant role in immunotherapy resistance by excluding T-cells from tumors. FAP⁺ CAFs can protect tumor cells from tumor necrosis factor and interferon-mediated T-cell necrosis and can express CXC motif chemokine ligands, inhibiting T-cells from accessing tumor cells. ECM remodeling by CAFs also creates a physical barrier preventing immune cell infiltration. The interplay between CAFs and tumor immunosuppressive cells is vital in discovering new ways to promote immunogenic cancer cell death. The degradation, suppression, or reduction of CAFs have been shown to reduce immunosuppressive cells and allow an increased T-cell mediated anti-tumor effect (Antonia et al., 2016). As previously described, the CAF-secretion of IL-6 and IL-8 can promote tumor growth. CAFs aggregate macrophages and activate the NF-κB pathway through the secretion of IL-6 and IL-8, resulting in tumor immunosuppression (Su et al., 2018).

In a scRNA-seq study of a subpopulation of CAFs called CAF-S1 from breast cancer, it was observed that by promoting the attraction, survival, and total quantity of CD4⁺/CD25⁺/FOXP3⁺ regulatory T-cells in the TME, these CAFs promote immunosuppression. More specifically associated with the immunosuppressive environment were the clusters ECM-myCAF and TGFβ-myCAF. The abundance of these clusters correlates with that of PD-1⁺ and CTLA4⁺ CD4⁺ T-cells. The expression of PD-1 and CTLA4 at the surface of FOXP3⁺ T regulatory cells is upregulated by the ECM-myCAFs. Conversely, CD4⁺ CD25⁺ T lymphocytes promote the transformation of ECM-myCAF into TGFβ-myCAF fibroblasts. All these findings allude to the crosstalk between specific CAF clusters and T-lymphocytes that plays a role in immunosuppression and immunotherapy resistance (Kieffer et al., 2020). CAFs also directly contribute to T-cell suppression and deactivation by emulating APCs. In this mechanism, the antigen complexed with MHC-I is processed and presented by these fibroblasts, followed by co-incident antigen-specific upregulation of PD-1/PD-L2 and FAS/FASL on CAFs and T-cells, respectively. The result is enhanced tumor viability due to the dysfunction and death of T-cells (Lakins et al., 2018b). Therefore, the relationship between the TME and breast cancer cells, which is intricately intertwined with the CAF and inflammatory cells, has enormous potential for advancements in the treatment of breast cancer.

A popular approach to targeting CAFs and their tumor-promoting effects includes CAF reprogramming or reversion to a quiescent phenotype. CAF-rich tumors exclude CD8⁺ T-cells at the tumor margin and upregulate the expression of CTLA-4. A result of this exclusion is the induction of resistance to various immunotherapies, even those that include therapeutic vaccination and αPD1. A study showed that myofibroblastic CAF differentiation is regulated by the enzyme NADPH oxidase-4 (NOX4), and inhibiting this enzyme can transform these myofibroblastic CAFs back to a quiescent, fibroblast-like phenotype (Hanley et al., 2017). Upon further examination using a small-molecule NOX4/1 inhibitor [GKT137831 (setanaxib), genyotex] to target this pathway, it was observed that these drugs could surpass CAF-mediated immunotherapy resistance. These drugs significantly increased CD8⁺ T-cell infiltration into tumors, efficiently reversed CAF differentiation in vivo, and enhanced the immunotherapy response (Hanley and Thomas, 2020). Other targeting strategies include targeting ECM to allow drug access to tumor cells, TGF-β1 inhibition to prevent tumor progression by facilitating T cell infiltration, and reprogramming CAFs back to a quiescent state by using vitamin A and D agonists to increase the efficacy of chemotherapy (Sherman et al., 2014; Shany et al., 2016; Liu et al., 2019b). Moreover, Hh inhibition remained a significant target in cancer types such as PDAC, where activated CAFs were seen to have elevated Hh signaling and corresponding iCAF production leading to more regulatory T-cells and increased immunosuppression (Steele et al., 2021). Other approaches involve the use of viral vaccines to broaden the cytotoxic range of therapy effects on tumor cells, and CAFs combined (Chen et al., 2015), CAF-directed drug conjugates, inhibition of CTLA-4 and PD-L1 stagnating tumor progression by increasing intratumoral CD8⁺and CD4⁺ T-cells while reducing T regulatory cell count and overall immunosuppressive actions (Fiegle et al., 2019), CXCL12 and CXCR4 inhibition of induced metastasis and invasiveness (Izumi et al., 2016), targeting CAF immune evasion mechanisms, and finally CAF depletion. In many cancers, TAM overexpresses CSF-1R receptors that control macrophages’ production, differentiation, and function. In a murine model, a CSF-1R inhibitor increased T-cell infiltration and CD8⁺ T-cell activity, reduced the recruitment of bone marrow-derived suppressor cells (BMDSC), and suppressed the generation of inflammatory mediators in TAM. As a result of the inhibition of CSF-1R, CAFs neutralized the inhibitor by secreting chemokines and chemokine ligands. The addition of a chemokine receptor antagonist decreased the tumor burden, and the addition of an immune checkpoint inhibitor (anti-PD-1) entirely stopped tumor growth (Kumar et al., 2017). Methods of targeting CAF populations related to immune modulation in the tumor microenvironment can prove to be effective in countering the effects of CAF-induced immunotherapy resistance.