circ-ZEB1 regulates epithelial-mesenchymal transition and chemotherapy resistance of colorectal cancer through acting on miR-200c-5p

• Published in: Translational oncology 2023-02, Vol.28, p.101604-101604, Article 101604
• Main Authors: Chen, Hongyu, Zhang, Jianwei, Yang, Lei, Li, Yansen, Wang, Zhenjun, Ye, Chunxiang
• Format: Article
• Language: English
• Subjects: Chemoresistance; circ-ZEB1; Colorectal cancer; EMT; miR-200c
• ISSN: 1936-5233
• DOI: 10.1016/j.tranon.2022.101604

•circ-ZEB1 is highly expressed in colorectal cancer tissues.•circ-ZEB1 knocking down inhibits CRC cells proliferation and metastasis in vitro and in vivo.•circ-ZEB1 regulates EMT and chemotherapeutic resistance in CRC cells.•circ-ZEB1 exerts its regulatory effect through sponging miR-200c.•Our research provides new targets for colorectal cancer treatment. Circular RNAs (circRNAs) have been demonstrated to be important regulators in human malignant tumors, including colorectal cancer (CRC). While the role circ-ZEB1 played in CRC remains unclear. In this study, we aim to explore the biological function and the underlying mechanism of circ-ZEB1 in CRC. RNAscope was used to analyze the expression and localization of circ-ZEB1 in CRC tissues. Loss of function experiments were conducted, including CCK-8, transwell assays, flow cytometry analysis, and murine xenograft models, so as to detect the effect of circ-ZEB1 on CRC cells. IC50 assay was used to evaluate the influence of circ-ZEB1 on the chemoresistance of CRC cells. Epithelial-mesenchymal transition (EMT) related markers were detected. The relationship between circ-ZEB1 and miR-200c-5p was investigated by FISH, dual-luciferase reporter assay, and RIP assay. We found in our study that circ-ZEB1 was significantly upregulated in CRC tissues. Downregulation of circ-ZEB1 inhibited cell proliferation, colony formation, as well as cell migration and invasion abilities of CRC cell lines. In vivo experiments indicated that knockdown of circ-ZEB1 suppressed tumorigenesis and distant metastasis of CRC cells in nude mice. What's more, EMT and chemoresistance of CRC cells were also attenuated following circ-ZEB1 knockdown. Mechanistically, we proved that circ-ZEB1 could directly bind with miR-200c and functioned as miR-200c sponge to exert its biological functions in CRC cells. In conclusion, circ-ZEB1 could promote CRC cells progression, EMT, and chemoresistance via acting on miR-200c, elucidating a potential therapeutic target to inhibit CRC progression. [Display omitted]