期刊论文详细信息
Biological research: BR
Mir-30b-3p affects the migration and invasion function of ovarian cancer cells by targeting the CTHRC1 gene
article
Li, Yan1  Zhou, Jinhua1  Wang, Juan1  Chen, Xiaoping2  Zhu, Yan2  Chen, Youguo1 
[1]Department of Obstetrics and Gynecology, The First Affiliated Hospital of Soochow University
[2]Department of Obstetrics and Gynecology, The First People’s Hospital of Yancheng
关键词: miR-30b-3p;    Ovarian cancer;    OVCAR3;    CTHRC1;    EMT;   
DOI  :  10.1186/s40659-020-00277-4
来源: BioMed Central
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【 摘 要 】
The aim of this study was to investigate the effect role and mechanism of miR-30b-3p on ovarian cancer cells biological function. The expression of miR-30b-3p was detected in ovarian cancer cell lines and normal ovarian epithelial cell line by qRT-PCR. Mir-30b-3p mimic was transfected into OVCAR3 cells. Cell-counting kit-8 (CCK-8) assay was conducted to explore the effect of mir-30b-3p on the OVCAR3 cells’ proliferation. Cell cycle and apoptosis were detected by Flow cytometry. Cell invasion ability was detected by Transwell test. The regulation of putative target of miR-30b-3p was verified by double luciferase reporter assays and Western blot. We found that miR-30b-3p was downregulated in OVCAR3 cells. Overexpression of miR-30b-3p suppressed proliferation, promoted apoptosis, slowed cell cycle and inhibited migration and invasion of OVCAR3 cells. Bioinformatics analysis identified 3′-untranslated region (3′UTR) of Collagen triple helix repeat-containing 1 (CTHRC1) as the presumed binding site for miR-30b-3p. Detection of double luciferase reporter and Western-Blot result confirmed that CTHRC1 was the target gene of miR-30b-3p. Furthermore, E-cadherin, β-cadherin and Vimentin protein expression level were changed after transfection of miR-30b-3p. miR-30b-3p function as an anti-cancer gene. Overexpression of miR-30b-3p can inhibit the biological function of ovarian cancer cells. MiR-30b-3p targets CTHRC1 gene plays an important role in epithelial–mesenchymal transformation (EMT), and supports miR-30b-3p as a potential biological indicator for ovarian cancer in the future.
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