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CAF-Related Signaling Pathways in NSCLC: Comparison
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Please note this is a comparison between Version 2 by Catherine Yang and Version 1 by Yasushi Shintani.

In the tumor microenvironment, cancer-associated fibroblasts (CAFs) have multiple tumor-promoting functions in drug resistance, regulation of the niche of cancer stem cells and formation of the immunosuppressive network. Lung cancer is the most frequently diagnosed cancer and the leading cause of cancer death worldwide. The most common lung cancer is non-small cell lung cancer (NSCLC), with an overall 5-year survival rate of around 20% because NSCLC is a metastatic disease. CAFs interact with lung cancer cells to allow for the acquisition of malignancy and treatment resistance by paracrine loops via EMT signals in the tumor microenvironment

  • non-small cell lung cancer
  • tumor microenvironment
  • cancer-associated fibroblasts

1. Signaling Pathways between CAFs and NSCLC

Cancer initiates fibroblast transition with acquisition of CAF phenotypes via cancer-derived growth factors, as well as cytokines that regulate the TGF-β and NF-κB signaling pathways [1]. We have previously shown that TGF-β secreted from NSCLC cancer cells activates fibroblasts in the tumor microenvironment [2]. CAFs secrete growth factors, including TGF-β, FGF2/7, PDGF, and HGF, as well as VEGF, which promote cancer cell proliferation [3]. Resident fibroblasts are also activated and change to proinflammatory CAFs during the early preneoplastic stages of tumorigenesis [4]. Activated CAFs produce higher amounts of SDF-1 than lung normal fibroblasts (LNFs), and SDF-1 facilitates cancer cell proliferation and chemoresistance via the CXCR4-mediated signaling pathway, which involves NF-κB and Bcl-xL [5]. MAPK, PI3K/mTOR, and Wnt/β-catenin signaling are also activated in cancer cells in response to CAF-derived growth factors and cytokines. The JAK/STAT pathway are activated by CAF-derived IL-6, IL-10, IL-11, and IL-22 [6]. We previously reported that NSCLC cells underwent EMT and acquired stem-cell-like properties when cocultured with CAFs isolated from surgical exploration [7]. IL-6 from CAFs enhanced EMT and chemoresistance in NSCLC cells, suggesting a role of IL-6 in the maintenance of a paracrine loop that functions as part of the communication between CAFs and NSCLC cells [2][8]. Similarly, CAF-derived CXCL1, IL-6, and COX-2, known targets of the NF-κB transcription factor, reportedly correlate with tumor-promoting inflammation and tumor invasiveness [9][10]. Iwai et al. reported altered gene expression in NSCLC CAFs compared to LNFs using capped analysis of gene expression to comprehensively analyze promoter activity in CAFs [11]. Among 390 genes highly expressed in NSCLC CAFs, they identified COLXIα1, integrin α11, and COL1A1 as CAF-specific genes that promote CAFs migration toward collagen type I and fibronectin via ERK1/2. Thus, several different signaling pathways in CAF-mediated cancer progression have been extensively explored to determine their roles in the tumor microenvironment (Figure 1). All these signaling pathways in CAFs have potential as targets for blocking crosstalk between CAFs and cancer cells.
Figure 1. Crosstalk of signaling pathways among CAFs, NSCLC cells, and immune cells. TGF-β and exosomes secreted from NSCLC cancer cells activate fibroblasts into CAFs in the tumor microenvironment. The production of growth factors, cytokines, chemokines, and exosomes from CAFs contribute to NSCLC cell proliferation, chemoresistance, angiogenesis, immunomodulation, and ECM remodeling. These in turn change the tumor microenvironment and contribute to NSCLC progression. NFs, normal fibroblasts; CAFs, cancer-associated fibroblasts; NSCLC, non-small cell lung cancer; miRNA, microRNA; lncRNA, long non-coding RNA; TGF-β, transforming growth factor-β; FGF, fibroblast growth factor; PDGF, platelet-derived growth factor; HGF, hepatocyte growth factor; IL-6, interleukin-6; SDF-1, stromal cell-derived factor-1; Gas6, growth arrest-specific 6; IL-11, interleukin-11; IGF2, insulin-like growth factor 2; VEGF, vascular endothelial growth factor; CCL2, C-C motif chemokine 2; PGE2, prostaglandin E2; CXCL2, chemokine (C-X-C motif) ligand 2; MMP, matrix metalloproteinase; ECM, extracellular matrix.

2. Role of CAFs in Resistance to Antitumor Therapy

EMT resulted in increased malignant potential and reduced sensitivity to chemotherapy in NSCLC cells [12]. Furthermore, chronic exposure to anticancer drugs or radiation resulted in cells forming therapy-resistant sublines that underwent EMT via interactions between NSCLC cells and CAFs through the TGF-β, and IL-6 pathways [2]. Exposure to anticancer drugs enhances IL-11 secretion by CAFs, which promotes chemoresistance of cancer cells through the STAT3 signaling pathway [10][13]. CAF expression of Gas6, a natural ligand of tumor-associated macrophage (TAM) receptors with high affinity for the receptor tyrosine kinase Axl, increases during chemotherapy and promotes proliferation and migration of NSCLC cells [14]. Tumoral Axl activation induces EMT and promotes cell survival and chemoresistance [15]. In addition, CAFs enhanced chemoresistance by repression of caspase-3 and caspase-8 through the activation of the annexin A3/JNK pathway [16]. CAFs also induce acquired chemoresistance through the IGF2/IGFR-1 paracrine pathway, which activates IGF2/AKT/Sox2/ABCB1 signaling and upregulation of P-glycoprotein expression in NSCLC cells [17]. Such data suggest that CAFs, in concert with tumor cells and other components of the tumor microenvironment, abet resistance to treatment [18].

3. Role of CAFs in Oncogene Addicted NSCLC

Numerous driver mutations have been identified in NSCLC, and oncogene addiction provides rationale for molecular targeted therapy [19]. Pellinen et al. recently explored associations of EGFR mutations and CAF subtypes using multiplex fluorescence immunohistochemistry; their findings indicated that gene alterations may affect the properties of CAFs in the tumor microenvironment [20]. That microenvironment provides sustained resistance to molecular targeted therapy. CAFs have a critical role in the resistance of lung cancer to EGFR TKIs through the induction of EMT via CAF-mediated signaling pathways [21][22]. Yoshida et al. also found that lung adenocarcinoma cell lines became more resistant to EGFR TKIs when cocultured with CAFs expressing podoplanin, suggesting that podoplanin-positive CAFs may be useful for predicting response to EGFR TKIs [23]. CAF-released IL-6 mediates NSCLC acquired resistance to EGFR TKIs through the JAK1/STAT3 pathway [24]. In addition, MET activation is an important mechanism for acquisition of resistance to TKIs [25]. Treatment of EGFR- or MET-addicted NSCLC cancer cells was shown to cause a metabolic shift toward increased glycolysis and lactate production, which develop chemoresistance in NSCLC cells [26]. Another study demonstrated that CAFs increase the expression and phosphorylation of annexin A2 by secretion of HGF and IGF-1, which regulate EMT and EGFR TKI resistance in a paracrine manner [22]. Together, these findings suggest that cotreatment targeting CAFs may further improve the antitumor efficacy of molecular targeted therapy.

4. Role of Extracellular Vesicles in Communication between CAFs and NSCLC

Exosomes carry and transfer a variety of cargo, including small non-coding RNAs, also known as miRNAs and lncRNAs, which have essential roles in cellular communication. Shen et al. compared miRNA expression profiles between CAFs from NSCLC and LNFs from matched healthy lungs and showed downregulation of miR-1 and miR-206 and upregulation of miR-31 in CAFs [27]. CAF-derived miRNAs also contribute to the transformation of LNFs into CAFs [28]. Furthermore, miR-210 in the exosome secreted by CAFs was taken up by NSCLC cells and promoted EMT by targeting UPF1, a key factor in a variety of RNA decay pathways, and activating the PTEN/PI3K pathway in cancer cells, thereby promoting NSCLC migration and invasion [29]. CAF-derived exosomes also exhibited miR-20a upregulation and promoted NSCLC cell proliferation and chemoresistance via PTEN downregulation following activation of the PI3K/AKT pathway [30]. Cancer cell-derived TGF-β1 activates miR-21 expression in LNFs and induces differentiation to CAFs, which promote the proliferation of cancer cells through the secretion of calumenin [31]. CAF-specific miR-196a promotes NSCLC progression via CCL2 secretion by directly targeting ANXA1 (the gene for annexin-A1) which has anti-inflammatory properties [32]. LncRNAs also participate in activation of LNFs to CAFs, whereas activated CAFs can change gene expression and secretion characteristics of NSCLC cells through lncRNAs [33]. Liu et al. screened fibroblast-specific lncRNAs using RNA-seq data and identified LINC01614 promoting the secretion of IL-6 from cancer cells that upregulates LINC01614 in CAFs, constituting a feedforward loop between CAFs and NSCLC cells [34].
Together, the dysregulation of exosomal miRNA and lncRNAs is involved in the dynamic crosstalk between CAFs and NSCLC cells.

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