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Cancer-associated fibroblasts in colorectal cancer
Kamali Zonouzi, S; Pezeshki, P. S.; Razi, S; Rezaei, Nima.
Affiliation
  • Kamali Zonouzi, S; Tehran University of Medical Sciences. Tehran. Iran
  • Pezeshki, P. S.; Tehran University of Medical Sciences. Tehran. Iran
  • Razi, S; Universal Scientific Education and Research Network (USERN). Tehran. Iran
  • Rezaei, Nima; Children’s Medical Center. Tehran. Iran
Clin. transl. oncol. (Print) ; Clin. transl. oncol. (Print);24(5): 757-769, mayo 2022.
Article in En | IBECS | ID: ibc-203779
Responsible library: ES1.1
Localization: ES15.1 - BNCS
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.
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Full text: 1 Collection: 06-national / ES Database: IBECS Main subject: Carboxypeptidases / Colorectal Neoplasms / Tumor Microenvironment / Carcinogenesis / Cancer-Associated Fibroblasts Limits: Humans Language: En Journal: Clin. transl. oncol. (Print) Year: 2022 Document type: Article

Full text: 1 Collection: 06-national / ES Database: IBECS Main subject: Carboxypeptidases / Colorectal Neoplasms / Tumor Microenvironment / Carcinogenesis / Cancer-Associated Fibroblasts Limits: Humans Language: En Journal: Clin. transl. oncol. (Print) Year: 2022 Document type: Article