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Published in: Clinical and Translational Oncology 5/2022

01-05-2022 | Metastasis | Review Article

Cancer-associated fibroblasts in colorectal cancer

Authors: S. Kamali Zonouzi, P. S. Pezeshki, S. Razi, N. Rezaei

Published in: Clinical and Translational Oncology | Issue 5/2022

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Abstract

Colorectal cancer (CRC) is one of the leading causes of mortality among cancers. Many aspects of this cancer are under investigation to find established markers of diagnosis, prognosis, and also potential drug targets. In this review article, we are going to discuss the possible solution to all these aims by investigating the literature about cancer-associated fibroblasts (CAFs) involved in CRC. Moreover, we are going to review their interaction with the tumor microenvironment (TME) and vitamin D and their role in tumorigenesis and metastasis. Moreover, we are going to expand more on some markers produced by them or related to them including FAP, a-SMA, CXCL12, TGF- β, POSTN, and β1-Integrin. Some signaling pathways related to CAFs are as follows: FAK, AKT, activin A, and YAP/TAZ. Some genes related to the CAFs which are found to be possible therapeutic targets include COL3A1, JAM3, AEBP1 and, CAF-derived TGFB3, WNT2, and WNT54.
Literature
2.
go back to reference Cheng L, et al. Trends in colorectal cancer incidence by anatomic site and disease stage in the United States from 1976 to 2005. Am J Clin Oncol. 2011;34(6):573–80.PubMedCrossRef Cheng L, et al. Trends in colorectal cancer incidence by anatomic site and disease stage in the United States from 1976 to 2005. Am J Clin Oncol. 2011;34(6):573–80.PubMedCrossRef
3.
go back to reference Raftery L, Goldberg RM. Optimal delivery of cytotoxic chemotherapy for colon cancer. Cancer J. 2010;16(3):214–9.PubMedCrossRef Raftery L, Goldberg RM. Optimal delivery of cytotoxic chemotherapy for colon cancer. Cancer J. 2010;16(3):214–9.PubMedCrossRef
4.
go back to reference Vodenkova S, et al. 5-fluorouracil and other fluoropyrimidines in colorectal cancer: past, present and future. Pharmacol Ther. 2020;206:107447.PubMedCrossRef Vodenkova S, et al. 5-fluorouracil and other fluoropyrimidines in colorectal cancer: past, present and future. Pharmacol Ther. 2020;206:107447.PubMedCrossRef
5.
go back to reference Nissen NI, et al. Prognostic value of blood-based fibrosis biomarkers in patients with metastatic colorectal cancer receiving chemotherapy and bevacizumab. Sci Rep. 2021;11(1):865.PubMedPubMedCentralCrossRef Nissen NI, et al. Prognostic value of blood-based fibrosis biomarkers in patients with metastatic colorectal cancer receiving chemotherapy and bevacizumab. Sci Rep. 2021;11(1):865.PubMedPubMedCentralCrossRef
6.
go back to reference Hanahan D, Coussens LM. Accessories to the crime: functions of cells recruited to the tumor microenvironment. Cancer Cell. 2012;21(3):309–22.PubMedCrossRef Hanahan D, Coussens LM. Accessories to the crime: functions of cells recruited to the tumor microenvironment. Cancer Cell. 2012;21(3):309–22.PubMedCrossRef
7.
go back to reference Quante M, et al. Bone marrow-derived myofibroblasts contribute to the mesenchymal stem cell niche and promote tumor growth. Cancer Cell. 2011;19(2):257–72.PubMedPubMedCentralCrossRef Quante M, et al. Bone marrow-derived myofibroblasts contribute to the mesenchymal stem cell niche and promote tumor growth. Cancer Cell. 2011;19(2):257–72.PubMedPubMedCentralCrossRef
8.
9.
go back to reference Wu X, et al. Repurposing vitamin D for treatment of human malignancies via targeting tumor microenvironment. Acta Pharm Sin B. 2019;9(2):203–19.PubMedCrossRef Wu X, et al. Repurposing vitamin D for treatment of human malignancies via targeting tumor microenvironment. Acta Pharm Sin B. 2019;9(2):203–19.PubMedCrossRef
10.
go back to reference Fujita M, et al. Peptide TNIIIA2 derived from Tenascin-C contributes to malignant progression in colitis-associated colorectal cancer via β1-Integrin activation in fibroblasts. Int J Mol Sci. 2019;20(11):2752.PubMedCentralCrossRef Fujita M, et al. Peptide TNIIIA2 derived from Tenascin-C contributes to malignant progression in colitis-associated colorectal cancer via β1-Integrin activation in fibroblasts. Int J Mol Sci. 2019;20(11):2752.PubMedCentralCrossRef
11.
go back to reference Kasashima H, et al. Stromal SOX2 upregulation promotes tumorigenesis through the generation of a SFRP1/2-expressing cancer-associated fibroblast population. Dev Cell. 2021;56(1):95-110.e10.PubMedCrossRef Kasashima H, et al. Stromal SOX2 upregulation promotes tumorigenesis through the generation of a SFRP1/2-expressing cancer-associated fibroblast population. Dev Cell. 2021;56(1):95-110.e10.PubMedCrossRef
12.
go back to reference Herrera A, et al. Endothelial cell activation on 3D-matrices derived from PDGF-BB-stimulated fibroblasts is mediated by Snail1. Oncogenesis. 2018;7(9):76.PubMedPubMedCentralCrossRef Herrera A, et al. Endothelial cell activation on 3D-matrices derived from PDGF-BB-stimulated fibroblasts is mediated by Snail1. Oncogenesis. 2018;7(9):76.PubMedPubMedCentralCrossRef
13.
go back to reference Huang, T.X., et al. Targeting cancer-associated fibroblast-secreted WNT2 restores dendritic cell-mediated antitumour immunity. Gut 2021:322924. Huang, T.X., et al. Targeting cancer-associated fibroblast-secreted WNT2 restores dendritic cell-mediated antitumour immunity. Gut 2021:322924.
14.
go back to reference Unterleuthner D, et al. Cancer-associated fibroblast-derived WNT2 increases tumor angiogenesis in colon cancer. Angiogenesis. 2020;23(2):159–77.PubMedCrossRef Unterleuthner D, et al. Cancer-associated fibroblast-derived WNT2 increases tumor angiogenesis in colon cancer. Angiogenesis. 2020;23(2):159–77.PubMedCrossRef
15.
go back to reference Coto-Llerena M, et al. High expression of FAP in colorectal cancer is associated with angiogenesis and immunoregulation processes. Front Oncol. 2020;10:979.PubMedPubMedCentralCrossRef Coto-Llerena M, et al. High expression of FAP in colorectal cancer is associated with angiogenesis and immunoregulation processes. Front Oncol. 2020;10:979.PubMedPubMedCentralCrossRef
16.
go back to reference Nishishita R, et al. Expression of cancer-associated fibroblast markers in advanced colorectal cancer. Oncol Lett. 2018;15(5):6195–202.PubMedPubMedCentral Nishishita R, et al. Expression of cancer-associated fibroblast markers in advanced colorectal cancer. Oncol Lett. 2018;15(5):6195–202.PubMedPubMedCentral
17.
go back to reference Solano-Iturri JD, et al. Altered expression of fibroblast activation protein-α (FAP) in colorectal adenoma-carcinoma sequence and in lymph node and liver metastases. Aging (Albany NY). 2020;12(11):10337–58.CrossRef Solano-Iturri JD, et al. Altered expression of fibroblast activation protein-α (FAP) in colorectal adenoma-carcinoma sequence and in lymph node and liver metastases. Aging (Albany NY). 2020;12(11):10337–58.CrossRef
18.
go back to reference Chen L, et al. FAP positive fibroblasts induce immune checkpoint blockade resistance in colorectal cancer via promoting immunosuppression. Biochem Biophys Res Commun. 2017;487(1):8–14.PubMedCrossRef Chen L, et al. FAP positive fibroblasts induce immune checkpoint blockade resistance in colorectal cancer via promoting immunosuppression. Biochem Biophys Res Commun. 2017;487(1):8–14.PubMedCrossRef
19.
go back to reference Wanandi SI, et al. Cancer-associated fibroblast (CAF) secretomes-induced epithelial-mesenchymal transition on HT-29 colorectal carcinoma cells associated with hepatocyte growth factor (HGF) signalling. J Pak Med Assoc. 2021;71(2):S18–24 (Suppl 2).PubMed Wanandi SI, et al. Cancer-associated fibroblast (CAF) secretomes-induced epithelial-mesenchymal transition on HT-29 colorectal carcinoma cells associated with hepatocyte growth factor (HGF) signalling. J Pak Med Assoc. 2021;71(2):S18–24 (Suppl 2).PubMed
20.
go back to reference Herrera M, et al. Cancer-associated fibroblast and M2 macrophage markers together predict outcome in colorectal cancer patients. Cancer Sci. 2013;104(4):437–44.PubMedPubMedCentralCrossRef Herrera M, et al. Cancer-associated fibroblast and M2 macrophage markers together predict outcome in colorectal cancer patients. Cancer Sci. 2013;104(4):437–44.PubMedPubMedCentralCrossRef
21.
22.
go back to reference Mochizuki S, et al. Expression and function of a disintegrin and metalloproteinases in cancer-associated fibroblasts of colorectal cancer. Digestion. 2020;101(1):18–24.PubMedCrossRef Mochizuki S, et al. Expression and function of a disintegrin and metalloproteinases in cancer-associated fibroblasts of colorectal cancer. Digestion. 2020;101(1):18–24.PubMedCrossRef
23.
go back to reference Yang T, et al. Increased RAB31 expression in cancer-associated fibroblasts promotes colon cancer progression through HGF-MET signaling. Front Oncol. 2020;10:1747.PubMedPubMedCentralCrossRef Yang T, et al. Increased RAB31 expression in cancer-associated fibroblasts promotes colon cancer progression through HGF-MET signaling. Front Oncol. 2020;10:1747.PubMedPubMedCentralCrossRef
24.
go back to reference Gu C, Lu H, Qian Z. Matrine reduces the secretion of exosomal circSLC7A6 from cancer-associated fibroblast to inhibit tumorigenesis of colorectal cancer by regulating CXCR5. Biochem Biophys Res Commun. 2020;527(3):638–45.PubMedCrossRef Gu C, Lu H, Qian Z. Matrine reduces the secretion of exosomal circSLC7A6 from cancer-associated fibroblast to inhibit tumorigenesis of colorectal cancer by regulating CXCR5. Biochem Biophys Res Commun. 2020;527(3):638–45.PubMedCrossRef
25.
go back to reference Ma H, et al. Periostin promotes colorectal tumorigenesis through integrin-FAK-Src pathway-mediated YAP/TAZ activation. Cell Rep. 2020;30(3):793-806.e6.PubMedCrossRef Ma H, et al. Periostin promotes colorectal tumorigenesis through integrin-FAK-Src pathway-mediated YAP/TAZ activation. Cell Rep. 2020;30(3):793-806.e6.PubMedCrossRef
26.
go back to reference Thongchot S, et al. Periostin regulates autophagy through integrin α5β1 or α6β4 and an AKT-dependent pathway in colorectal cancer cell migration. J Cell Mol Med. 2020;24(21):12421–32.PubMedPubMedCentralCrossRef Thongchot S, et al. Periostin regulates autophagy through integrin α5β1 or α6β4 and an AKT-dependent pathway in colorectal cancer cell migration. J Cell Mol Med. 2020;24(21):12421–32.PubMedPubMedCentralCrossRef
27.
go back to reference Chen, W., et al. CaMKII mediates TGFβ1-induced fibroblasts activation and its cross talk with colon cancer cells. Dig Dis Sci. 2021. Chen, W., et al. CaMKII mediates TGFβ1-induced fibroblasts activation and its cross talk with colon cancer cells. Dig Dis Sci. 2021.
28.
go back to reference Tanabe Y, et al. Blockade of the chemokine receptor, CCR5, reduces the growth of orthotopically injected colon cancer cells via limiting cancer-associated fibroblast accumulation. Oncotarget. 2016;7(30):48335–45.PubMedPubMedCentralCrossRef Tanabe Y, et al. Blockade of the chemokine receptor, CCR5, reduces the growth of orthotopically injected colon cancer cells via limiting cancer-associated fibroblast accumulation. Oncotarget. 2016;7(30):48335–45.PubMedPubMedCentralCrossRef
29.
go back to reference Stadler S, et al. Colon cancer cell-derived 12(S)-HETE induces the retraction of cancer-associated fibroblast via MLC2, RHO/ROCK and Ca(2+) signalling. Cell Mol Life Sci. 2017;74(10):1907–21.PubMedCrossRef Stadler S, et al. Colon cancer cell-derived 12(S)-HETE induces the retraction of cancer-associated fibroblast via MLC2, RHO/ROCK and Ca(2+) signalling. Cell Mol Life Sci. 2017;74(10):1907–21.PubMedCrossRef
30.
go back to reference Herrera M, et al. Differential distribution and enrichment of non-coding RNAs in exosomes from normal and cancer-associated fibroblasts in colorectal cancer. Mol Cancer. 2018;17(1):114.PubMedPubMedCentralCrossRef Herrera M, et al. Differential distribution and enrichment of non-coding RNAs in exosomes from normal and cancer-associated fibroblasts in colorectal cancer. Mol Cancer. 2018;17(1):114.PubMedPubMedCentralCrossRef
31.
go back to reference Bhome R, et al. Exosomal microRNAs derived from colorectal cancer-associated fibroblasts: role in driving cancer progression. Aging (Albany NY). 2017;9(12):2666–94.CrossRef Bhome R, et al. Exosomal microRNAs derived from colorectal cancer-associated fibroblasts: role in driving cancer progression. Aging (Albany NY). 2017;9(12):2666–94.CrossRef
32.
go back to reference Fourniols T, et al. Inhibition of colorectal cancer-associated fibroblasts by lipid nanocapsules loaded with acriflavine or paclitaxel. Int J Pharm. 2020;584:119337.PubMedCrossRef Fourniols T, et al. Inhibition of colorectal cancer-associated fibroblasts by lipid nanocapsules loaded with acriflavine or paclitaxel. Int J Pharm. 2020;584:119337.PubMedCrossRef
33.
go back to reference Wawro ME, et al. Nonsteroidal anti-inflammatory drugs prevent vincristine-dependent cancer-associated fibroblasts formation. Int J Mol Sci. 2019;20(8):1941.PubMedCentralCrossRef Wawro ME, et al. Nonsteroidal anti-inflammatory drugs prevent vincristine-dependent cancer-associated fibroblasts formation. Int J Mol Sci. 2019;20(8):1941.PubMedCentralCrossRef
34.
go back to reference Yadav VK, et al. Preclinical evaluation of the novel small-molecule MSI-N1014 for treating drug-resistant colon cancer via the LGR5/β-catenin/miR-142-3p network and reducing cancer-associated fibroblast transformation. Cancers (Basel). 2020;12(6):1590.PubMedCentralCrossRef Yadav VK, et al. Preclinical evaluation of the novel small-molecule MSI-N1014 for treating drug-resistant colon cancer via the LGR5/β-catenin/miR-142-3p network and reducing cancer-associated fibroblast transformation. Cancers (Basel). 2020;12(6):1590.PubMedCentralCrossRef
36.
37.
go back to reference Bauer J, et al. Increased stiffness of the tumor microenvironment in colon cancer stimulates cancer associated fibroblast-mediated prometastatic activin A signaling. Sci Rep. 2020;10(1):50.PubMedPubMedCentralCrossRef Bauer J, et al. Increased stiffness of the tumor microenvironment in colon cancer stimulates cancer associated fibroblast-mediated prometastatic activin A signaling. Sci Rep. 2020;10(1):50.PubMedPubMedCentralCrossRef
38.
40.
go back to reference Kawano S, et al. Assessment of elasticity of colorectal cancer tissue, clinical utility, pathological and phenotypical relevance. Cancer Sci. 2015;106(9):1232–9.PubMedPubMedCentralCrossRef Kawano S, et al. Assessment of elasticity of colorectal cancer tissue, clinical utility, pathological and phenotypical relevance. Cancer Sci. 2015;106(9):1232–9.PubMedPubMedCentralCrossRef
43.
go back to reference Olsen AL, et al. Hepatic stellate cells require a stiff environment for myofibroblastic differentiation. Am J Physiol Gastrointest Liver Physiol. 2011;301(1):G110–8.PubMedPubMedCentralCrossRef Olsen AL, et al. Hepatic stellate cells require a stiff environment for myofibroblastic differentiation. Am J Physiol Gastrointest Liver Physiol. 2011;301(1):G110–8.PubMedPubMedCentralCrossRef
44.
go back to reference Perepelyuk M, et al. Hepatic stellate cells and portal fibroblasts are the major cellular sources of collagens and lysyl oxidases in normal liver and early after injury. Am J Physiol Gastrointest Liver Physiol. 2013;304(6):G605–14.PubMedPubMedCentralCrossRef Perepelyuk M, et al. Hepatic stellate cells and portal fibroblasts are the major cellular sources of collagens and lysyl oxidases in normal liver and early after injury. Am J Physiol Gastrointest Liver Physiol. 2013;304(6):G605–14.PubMedPubMedCentralCrossRef
45.
go back to reference Bissell MJ, Hines WC. Why don’t we get more cancer? A proposed role of the microenvironment in restraining cancer progression. Nat Med. 2011;17(3):320–9.PubMedPubMedCentralCrossRef Bissell MJ, Hines WC. Why don’t we get more cancer? A proposed role of the microenvironment in restraining cancer progression. Nat Med. 2011;17(3):320–9.PubMedPubMedCentralCrossRef
46.
go back to reference Shibahara K, et al. Production of gastrointestinal tumors in mice by modulating latent TGF-β1 activation. Cancer Res. 2013;73(1):459–68.PubMedCrossRef Shibahara K, et al. Production of gastrointestinal tumors in mice by modulating latent TGF-β1 activation. Cancer Res. 2013;73(1):459–68.PubMedCrossRef
47.
go back to reference Zhou W, et al. Oxidative stress induced autophagy in cancer associated fibroblast enhances proliferation and metabolism of colorectal cancer cells. Cell Cycle. 2017;16(1):73–81.PubMedCrossRef Zhou W, et al. Oxidative stress induced autophagy in cancer associated fibroblast enhances proliferation and metabolism of colorectal cancer cells. Cell Cycle. 2017;16(1):73–81.PubMedCrossRef
48.
go back to reference Peng S, et al. Enhancing cancer-associated fibroblast fatty acid catabolism within a metabolically challenging tumor microenvironment drives colon cancer peritoneal metastasis. Mol Oncol. 2021;15:1391.PubMedPubMedCentralCrossRef Peng S, et al. Enhancing cancer-associated fibroblast fatty acid catabolism within a metabolically challenging tumor microenvironment drives colon cancer peritoneal metastasis. Mol Oncol. 2021;15:1391.PubMedPubMedCentralCrossRef
49.
go back to reference Abdul-Wahid A, et al. Serum-derived carcinoembryonic antigen (CEA) activates fibroblasts to induce a local re-modeling of the extracellular matrix that favors the engraftment of CEA-expressing tumor cells. Int J Cancer. 2018;143(8):1963–77.PubMedPubMedCentralCrossRef Abdul-Wahid A, et al. Serum-derived carcinoembryonic antigen (CEA) activates fibroblasts to induce a local re-modeling of the extracellular matrix that favors the engraftment of CEA-expressing tumor cells. Int J Cancer. 2018;143(8):1963–77.PubMedPubMedCentralCrossRef
51.
go back to reference Ferrer-Mayorga G, et al. Vitamin D receptor expression and associated gene signature in tumour stromal fibroblasts predict clinical outcome in colorectal cancer. Gut. 2017;66(8):1449–62.PubMedCrossRef Ferrer-Mayorga G, et al. Vitamin D receptor expression and associated gene signature in tumour stromal fibroblasts predict clinical outcome in colorectal cancer. Gut. 2017;66(8):1449–62.PubMedCrossRef
52.
go back to reference Demuytere J, et al. The role of the peritoneal microenvironment in the pathogenesis of colorectal peritoneal carcinomatosis. Exp Mol Pathol. 2020;115:104442.PubMedCrossRef Demuytere J, et al. The role of the peritoneal microenvironment in the pathogenesis of colorectal peritoneal carcinomatosis. Exp Mol Pathol. 2020;115:104442.PubMedCrossRef
53.
go back to reference González-González L, Alonso J. Periostin: a matricellular protein with multiple functions in cancer development and progression. Front Oncol. 2018;8:225.PubMedPubMedCentralCrossRef González-González L, Alonso J. Periostin: a matricellular protein with multiple functions in cancer development and progression. Front Oncol. 2018;8:225.PubMedPubMedCentralCrossRef
54.
55.
go back to reference Hardwick JC, et al. Bone morphogenetic protein 2 is expressed by, and acts upon, mature epithelial cells in the colon. Gastroenterology. 2004;126(1):111–21.PubMedCrossRef Hardwick JC, et al. Bone morphogenetic protein 2 is expressed by, and acts upon, mature epithelial cells in the colon. Gastroenterology. 2004;126(1):111–21.PubMedCrossRef
56.
go back to reference Beck SE, et al. BMP-induced growth suppression in colon cancer cells is mediated by p21WAF1 stabilization and modulated by RAS/ERK. Cell Signal. 2007;19(7):1465–72.PubMedPubMedCentralCrossRef Beck SE, et al. BMP-induced growth suppression in colon cancer cells is mediated by p21WAF1 stabilization and modulated by RAS/ERK. Cell Signal. 2007;19(7):1465–72.PubMedPubMedCentralCrossRef
57.
go back to reference Beck SE, et al. Bone morphogenetic protein signaling and growth suppression in colon cancer. Am J Physiol Gastrointest Liver Physiol. 2006;291(1):G135–45.PubMedCrossRef Beck SE, et al. Bone morphogenetic protein signaling and growth suppression in colon cancer. Am J Physiol Gastrointest Liver Physiol. 2006;291(1):G135–45.PubMedCrossRef
58.
go back to reference Flier SN, et al. Identification of epithelial to mesenchymal transition as a novel source of fibroblasts in intestinal fibrosis. J Biol Chem. 2010;285(26):20202–12.PubMedPubMedCentralCrossRef Flier SN, et al. Identification of epithelial to mesenchymal transition as a novel source of fibroblasts in intestinal fibrosis. J Biol Chem. 2010;285(26):20202–12.PubMedPubMedCentralCrossRef
59.
go back to reference Wu WK, et al. Bone morphogenetic protein signalling is required for the anti-mitogenic effect of the proteasome inhibitor MG-132 on colon cancer cells. Br J Pharmacol. 2008;154(3):632–8.PubMedPubMedCentralCrossRef Wu WK, et al. Bone morphogenetic protein signalling is required for the anti-mitogenic effect of the proteasome inhibitor MG-132 on colon cancer cells. Br J Pharmacol. 2008;154(3):632–8.PubMedPubMedCentralCrossRef
60.
go back to reference Zeisberg M, Shah AA, Kalluri R. Bone morphogenic protein-7 induces mesenchymal to epithelial transition in adult renal fibroblasts and facilitates regeneration of injured kidney. J Biol Chem. 2005;280(9):8094–100.PubMedCrossRef Zeisberg M, Shah AA, Kalluri R. Bone morphogenic protein-7 induces mesenchymal to epithelial transition in adult renal fibroblasts and facilitates regeneration of injured kidney. J Biol Chem. 2005;280(9):8094–100.PubMedCrossRef
61.
go back to reference Kosinski C, et al. Gene expression patterns of human colon tops and basal crypts and BMP antagonists as intestinal stem cell niche factors. Proc Natl Acad Sci USA. 2007;104(39):15418–23.PubMedPubMedCentralCrossRef Kosinski C, et al. Gene expression patterns of human colon tops and basal crypts and BMP antagonists as intestinal stem cell niche factors. Proc Natl Acad Sci USA. 2007;104(39):15418–23.PubMedPubMedCentralCrossRef
62.
go back to reference Namkoong H, et al. The bone morphogenetic protein antagonist gremlin 1 is overexpressed in human cancers and interacts with YWHAH protein. BMC Cancer. 2006;6:74.PubMedPubMedCentralCrossRef Namkoong H, et al. The bone morphogenetic protein antagonist gremlin 1 is overexpressed in human cancers and interacts with YWHAH protein. BMC Cancer. 2006;6:74.PubMedPubMedCentralCrossRef
63.
go back to reference Karagiannis GS, et al. Enrichment map profiling of the cancer invasion front suggests regulation of colorectal cancer progression by the bone morphogenetic protein antagonist, gremlin-1. Mol Oncol. 2013;7(4):826–39.PubMedPubMedCentralCrossRef Karagiannis GS, et al. Enrichment map profiling of the cancer invasion front suggests regulation of colorectal cancer progression by the bone morphogenetic protein antagonist, gremlin-1. Mol Oncol. 2013;7(4):826–39.PubMedPubMedCentralCrossRef
64.
go back to reference Lugli A, et al. Recommendations for reporting tumor budding in colorectal cancer based on the International Tumor Budding Consensus Conference (ITBCC) 2016. Mod Pathol. 2017;30(9):1299–311.PubMedCrossRef Lugli A, et al. Recommendations for reporting tumor budding in colorectal cancer based on the International Tumor Budding Consensus Conference (ITBCC) 2016. Mod Pathol. 2017;30(9):1299–311.PubMedCrossRef
65.
go back to reference Mitrovic B, et al. Tumor budding in colorectal carcinoma: time to take notice. Mod Pathol. 2012;25(10):1315–25.PubMedCrossRef Mitrovic B, et al. Tumor budding in colorectal carcinoma: time to take notice. Mod Pathol. 2012;25(10):1315–25.PubMedCrossRef
66.
go back to reference Sugai T, et al. Microenvironmental markers are correlated with lymph node metastasis in invasive submucosal colorectal cancer. Histopathology. 2021;79:584.PubMedPubMedCentralCrossRef Sugai T, et al. Microenvironmental markers are correlated with lymph node metastasis in invasive submucosal colorectal cancer. Histopathology. 2021;79:584.PubMedPubMedCentralCrossRef
67.
go back to reference Lee HO, et al. FAP-overexpressing fibroblasts produce an extracellular matrix that enhances invasive velocity and directionality of pancreatic cancer cells. BMC Cancer. 2011;11:245.PubMedPubMedCentralCrossRef Lee HO, et al. FAP-overexpressing fibroblasts produce an extracellular matrix that enhances invasive velocity and directionality of pancreatic cancer cells. BMC Cancer. 2011;11:245.PubMedPubMedCentralCrossRef
68.
go back to reference Kelly T, et al. Fibroblast activation protein-α: a key modulator of the microenvironment in multiple pathologies. Int Rev Cell Mol Biol. 2012;297:83–116.PubMedCrossRef Kelly T, et al. Fibroblast activation protein-α: a key modulator of the microenvironment in multiple pathologies. Int Rev Cell Mol Biol. 2012;297:83–116.PubMedCrossRef
69.
go back to reference Liu R, et al. Fibroblast activation protein: a potential therapeutic target in cancer. Cancer Biol Ther. 2012;13(3):123–9.PubMedCrossRef Liu R, et al. Fibroblast activation protein: a potential therapeutic target in cancer. Cancer Biol Ther. 2012;13(3):123–9.PubMedCrossRef
70.
go back to reference Kramer N, et al. Autocrine WNT2 signaling in fibroblasts promotes colorectal cancer progression. Oncogene. 2017;36(39):5460–72.PubMedCrossRef Kramer N, et al. Autocrine WNT2 signaling in fibroblasts promotes colorectal cancer progression. Oncogene. 2017;36(39):5460–72.PubMedCrossRef
71.
go back to reference Li J, et al. Carcinoma-associated fibroblasts lead the invasion of salivary gland adenoid cystic carcinoma cells by creating an invasive track. PLoS One. 2016;11(3):e0150247.PubMedPubMedCentralCrossRef Li J, et al. Carcinoma-associated fibroblasts lead the invasion of salivary gland adenoid cystic carcinoma cells by creating an invasive track. PLoS One. 2016;11(3):e0150247.PubMedPubMedCentralCrossRef
72.
go back to reference Gaggioli C, et al. Fibroblast-led collective invasion of carcinoma cells with differing roles for RhoGTPases in leading and following cells. Nat Cell Biol. 2007;9(12):1392–400.PubMedCrossRef Gaggioli C, et al. Fibroblast-led collective invasion of carcinoma cells with differing roles for RhoGTPases in leading and following cells. Nat Cell Biol. 2007;9(12):1392–400.PubMedCrossRef
73.
74.
go back to reference Chen SX, et al. Identification of colonic fibroblast secretomes reveals secretory factors regulating colon cancer cell proliferation. J Proteomics. 2014;110:155–71.PubMedCrossRef Chen SX, et al. Identification of colonic fibroblast secretomes reveals secretory factors regulating colon cancer cell proliferation. J Proteomics. 2014;110:155–71.PubMedCrossRef
75.
go back to reference Owusu BY, et al. Hepatocyte growth factor, a key tumor-promoting factor in the tumor microenvironment. Cancers (Basel). 2017;9(4):35.CrossRef Owusu BY, et al. Hepatocyte growth factor, a key tumor-promoting factor in the tumor microenvironment. Cancers (Basel). 2017;9(4):35.CrossRef
76.
go back to reference Satoh K, et al. Tumor budding in colorectal carcinoma assessed by cytokeratin immunostaining and budding areas: possible involvement of c-Met. Cancer Sci. 2014;105(11):1487–95.PubMedPubMedCentralCrossRef Satoh K, et al. Tumor budding in colorectal carcinoma assessed by cytokeratin immunostaining and budding areas: possible involvement of c-Met. Cancer Sci. 2014;105(11):1487–95.PubMedPubMedCentralCrossRef
77.
go back to reference Shangguan C, et al. Cancer-associated fibroblasts enhance tumor (18)F-FDG uptake and contribute to the intratumor heterogeneity of PET-CT. Theranostics. 2018;8(5):1376–88.PubMedPubMedCentralCrossRef Shangguan C, et al. Cancer-associated fibroblasts enhance tumor (18)F-FDG uptake and contribute to the intratumor heterogeneity of PET-CT. Theranostics. 2018;8(5):1376–88.PubMedPubMedCentralCrossRef
78.
go back to reference Chang AL, et al. CCL2 Produced by the glioma microenvironment is essential for the recruitment of regulatory T Cells and myeloid-derived suppressor cells. Cancer Res. 2016;76(19):5671–82.PubMedPubMedCentralCrossRef Chang AL, et al. CCL2 Produced by the glioma microenvironment is essential for the recruitment of regulatory T Cells and myeloid-derived suppressor cells. Cancer Res. 2016;76(19):5671–82.PubMedPubMedCentralCrossRef
79.
go back to reference Yang X, et al. FAP promotes immunosuppression by cancer-associated fibroblasts in the tumor microenvironment via STAT3-CCL2 signaling. Cancer Res. 2016;76(14):4124–35.PubMedCrossRef Yang X, et al. FAP promotes immunosuppression by cancer-associated fibroblasts in the tumor microenvironment via STAT3-CCL2 signaling. Cancer Res. 2016;76(14):4124–35.PubMedCrossRef
80.
go back to reference Hortobagyi, G.N., Edge S.B., Giuliano A. New and important changes in the TNM staging system for breast cancer. Am Soc Clin Oncol Educ Book. 2018;38:457–67.PubMedCrossRef Hortobagyi, G.N., Edge S.B., Giuliano A. New and important changes in the TNM staging system for breast cancer. Am Soc Clin Oncol Educ Book. 2018;38:457–67.PubMedCrossRef
81.
go back to reference Yan W, Shao R. Transduction of a mesenchyme-specific gene periostin into 293T cells induces cell invasive activity through epithelial-mesenchymal transformation. J Biol Chem. 2006;281(28):19700–8.PubMedCrossRef Yan W, Shao R. Transduction of a mesenchyme-specific gene periostin into 293T cells induces cell invasive activity through epithelial-mesenchymal transformation. J Biol Chem. 2006;281(28):19700–8.PubMedCrossRef
82.
go back to reference Xu X, et al. Periostin expression in intra-tumoral stromal cells is prognostic and predictive for colorectal carcinoma via creating a cancer-supportive niche. Oncotarget. 2016;7(1):798–813.PubMedCrossRef Xu X, et al. Periostin expression in intra-tumoral stromal cells is prognostic and predictive for colorectal carcinoma via creating a cancer-supportive niche. Oncotarget. 2016;7(1):798–813.PubMedCrossRef
83.
go back to reference Zheng X, et al. Epithelial-to-mesenchymal transition is dispensable for metastasis but induces chemoresistance in pancreatic cancer. Nature. 2015;527(7579):525–30.PubMedPubMedCentralCrossRef Zheng X, et al. Epithelial-to-mesenchymal transition is dispensable for metastasis but induces chemoresistance in pancreatic cancer. Nature. 2015;527(7579):525–30.PubMedPubMedCentralCrossRef
84.
go back to reference Sugai T, et al. Analysis of the expression of cancer-associated fibroblast- and EMT-related proteins in submucosal invasive colorectal cancer. J Cancer. 2018;9(15):2702–12.PubMedPubMedCentralCrossRef Sugai T, et al. Analysis of the expression of cancer-associated fibroblast- and EMT-related proteins in submucosal invasive colorectal cancer. J Cancer. 2018;9(15):2702–12.PubMedPubMedCentralCrossRef
85.
go back to reference Choi SY, et al. Podoplanin, α-smooth muscle actin or S100A4 expressing cancer-associated fibroblasts are associated with different prognosis in colorectal cancers. J Korean Med Sci. 2013;28(9):1293–301.PubMedPubMedCentralCrossRef Choi SY, et al. Podoplanin, α-smooth muscle actin or S100A4 expressing cancer-associated fibroblasts are associated with different prognosis in colorectal cancers. J Korean Med Sci. 2013;28(9):1293–301.PubMedPubMedCentralCrossRef
86.
87.
go back to reference Horman SR, et al. Functional profiling of microtumors to identify cancer associated fibroblast-derived drug targets. Oncotarget. 2017;8(59):99913–30.PubMedPubMedCentralCrossRef Horman SR, et al. Functional profiling of microtumors to identify cancer associated fibroblast-derived drug targets. Oncotarget. 2017;8(59):99913–30.PubMedPubMedCentralCrossRef
88.
go back to reference Zanotti S, et al. Opposing roles of miR-21 and miR-29 in the progression of fibrosis in Duchenne muscular dystrophy. Biochim Biophys Acta. 2015;1852(7):1451–64.PubMedCrossRef Zanotti S, et al. Opposing roles of miR-21 and miR-29 in the progression of fibrosis in Duchenne muscular dystrophy. Biochim Biophys Acta. 2015;1852(7):1451–64.PubMedCrossRef
89.
90.
go back to reference Layne MD, et al. Impaired abdominal wall development and deficient wound healing in mice lacking aortic carboxypeptidase-like protein. Mol Cell Biol. 2001;21(15):5256–61.PubMedPubMedCentralCrossRef Layne MD, et al. Impaired abdominal wall development and deficient wound healing in mice lacking aortic carboxypeptidase-like protein. Mol Cell Biol. 2001;21(15):5256–61.PubMedPubMedCentralCrossRef
91.
go back to reference Tumelty KE, et al. Aortic carboxypeptidase-like protein (ACLP) enhances lung myofibroblast differentiation through transforming growth factor β receptor-dependent and -independent pathways. J Biol Chem. 2014;289(5):2526–36.PubMedCrossRef Tumelty KE, et al. Aortic carboxypeptidase-like protein (ACLP) enhances lung myofibroblast differentiation through transforming growth factor β receptor-dependent and -independent pathways. J Biol Chem. 2014;289(5):2526–36.PubMedCrossRef
92.
go back to reference Gonçalves-Ribeiro S, et al. Carcinoma-associated fibroblasts affect sensitivity to oxaliplatin and 5FU in colorectal cancer cells. Oncotarget. 2016;7(37):59766–80.PubMedPubMedCentralCrossRef Gonçalves-Ribeiro S, et al. Carcinoma-associated fibroblasts affect sensitivity to oxaliplatin and 5FU in colorectal cancer cells. Oncotarget. 2016;7(37):59766–80.PubMedPubMedCentralCrossRef
93.
go back to reference Hanley CJ, et al. Targeting the myofibroblastic cancer-associated fibroblast phenotype through inhibition of NOX4. J Natl Cancer Inst. 2018;110(1):109–20.CrossRef Hanley CJ, et al. Targeting the myofibroblastic cancer-associated fibroblast phenotype through inhibition of NOX4. J Natl Cancer Inst. 2018;110(1):109–20.CrossRef
95.
go back to reference Fearon DT. The carcinoma-associated fibroblast expressing fibroblast activation protein and escape from immune surveillance. Cancer Immunol Res. 2014;2(3):187–93.PubMedCrossRef Fearon DT. The carcinoma-associated fibroblast expressing fibroblast activation protein and escape from immune surveillance. Cancer Immunol Res. 2014;2(3):187–93.PubMedCrossRef
97.
go back to reference Zadka Ł, et al. Interplay of stromal tumor-infiltrating lymphocytes, normal colonic mucosa, cancer-associated fibroblasts, clinicopathological data and the immunoregulatory molecules of patients diagnosed with colorectal cancer. Cancer Immunol Immunother. 2021;70(9):2681–700.PubMedPubMedCentralCrossRef Zadka Ł, et al. Interplay of stromal tumor-infiltrating lymphocytes, normal colonic mucosa, cancer-associated fibroblasts, clinicopathological data and the immunoregulatory molecules of patients diagnosed with colorectal cancer. Cancer Immunol Immunother. 2021;70(9):2681–700.PubMedPubMedCentralCrossRef
99.
go back to reference Kato T, et al. Cancer-associated fibroblasts affect intratumoral CD8(+) and FoxP3(+) T cells via IL6 in the tumor microenvironment. Clin Cancer Res. 2018;24(19):4820–33.PubMedCrossRef Kato T, et al. Cancer-associated fibroblasts affect intratumoral CD8(+) and FoxP3(+) T cells via IL6 in the tumor microenvironment. Clin Cancer Res. 2018;24(19):4820–33.PubMedCrossRef
100.
go back to reference Patsalias A, Kozovska Z. Personalized medicine: stem cells in colorectal cancer treatment. Biomed Pharmacother. 2021;141:111821.PubMedCrossRef Patsalias A, Kozovska Z. Personalized medicine: stem cells in colorectal cancer treatment. Biomed Pharmacother. 2021;141:111821.PubMedCrossRef
101.
go back to reference Xu H, et al. Cholesterol metabolism: new functions and therapeutic approaches in cancer. Biochim Biophys Acta Rev Cancer. 2020;1874(1):188394.PubMedCrossRef Xu H, et al. Cholesterol metabolism: new functions and therapeutic approaches in cancer. Biochim Biophys Acta Rev Cancer. 2020;1874(1):188394.PubMedCrossRef
103.
go back to reference Boonstra PA, et al. Clinical utility of circulating tumor DNA as a response and follow-up marker in cancer therapy. Cancer Metastasis Rev. 2020;39(3):999–1013.PubMedPubMedCentralCrossRef Boonstra PA, et al. Clinical utility of circulating tumor DNA as a response and follow-up marker in cancer therapy. Cancer Metastasis Rev. 2020;39(3):999–1013.PubMedPubMedCentralCrossRef
105.
106.
108.
go back to reference Barua I, et al. Artificial intelligence for polyp detection during colonoscopy: a systematic review and meta-analysis. Endoscopy. 2021;53(3):277–84.PubMedCrossRef Barua I, et al. Artificial intelligence for polyp detection during colonoscopy: a systematic review and meta-analysis. Endoscopy. 2021;53(3):277–84.PubMedCrossRef
109.
go back to reference Norton J, et al. Pancreatic cancer associated fibroblasts (CAF): under-explored target for pancreatic cancer treatment. Cancers (Basel). 2020;12(5):1347.CrossRef Norton J, et al. Pancreatic cancer associated fibroblasts (CAF): under-explored target for pancreatic cancer treatment. Cancers (Basel). 2020;12(5):1347.CrossRef
110.
go back to reference Leask A. A centralized communication network: recent insights into the role of the cancer associated fibroblast in the development of drug resistance in tumors. Semin Cell Dev Biol. 2020;101:111–4.PubMedCrossRef Leask A. A centralized communication network: recent insights into the role of the cancer associated fibroblast in the development of drug resistance in tumors. Semin Cell Dev Biol. 2020;101:111–4.PubMedCrossRef
Metadata
Title
Cancer-associated fibroblasts in colorectal cancer
Authors
S. Kamali Zonouzi
P. S. Pezeshki
S. Razi
N. Rezaei
Publication date
01-05-2022
Publisher
Springer International Publishing
Published in
Clinical and Translational Oncology / Issue 5/2022
Print ISSN: 1699-048X
Electronic ISSN: 1699-3055
DOI
https://doi.org/10.1007/s12094-021-02734-2

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