Literature DB >> 31063232

MicroRNA-26a-5p inhibits breast cancer cell growth by suppressing RNF6 expression.

Zi-Ming Huang1, Heng-Fa Ge1, Chen-Chen Yang1, Yong Cai1, Zhen Chen1, Wen-Ze Tian2, Jia-Li Tao3.   

Abstract

MicroRNA-26a-5p (miR-26a-5p) has been reported to be involved in the tumorigenesis of several tumors, but its function in breast cancer is still unknown. In this study, miR-26a-5p was found significantly downregulated in both of the breast cancer tissues and cell lines, and low expression of miR-26a-5p predicted a poor prognosis for breast cancer patients. Overexpression of miR-26a-5p could significantly inhibit breast cancer cell growth. Further studies revealed that overexpression of miR-26a-5p downregulated the protein levels of Cyclin D1, CDK4, and CDK6, but upregulated the expression levels of p21, p27, and p53. In mechanism, miR-26a-5p targeted the 3'UTR of ring finger protein 6 (RNF6) mRNA and inhibited RNF6 expression in breast cancer cells. Moreover, overexpression of miR-26a-5p inhibited RNF6/ERα/Bcl-xL axis in breast cancer cells. In contrast, inhibiting miR-26a-5p upregulated RNF6/ERα/Bcl-xL axis. Further studies indicated that miR-26a-5p mediated RNF6/ERα/Bcl-xL axis through regulating the stability of ERα protein. Collectively, downregulation of miR-26a-5p plays essential roles in breast cancer by mediating RNF6/ERα/Bcl-xL axis, which might provide important implications for the therapeutics of breast cancer.
© 2019 The Authors. The Kaohsiung Journal of Medical Sciences published by John Wiley & Sons Australia on behalf of Kaohsiung Medical University.

Entities:  

Keywords:  Bcl-xL; ERα; RNF6; breast cancer; microRNA-26a-5p

Mesh:

Substances:

Year:  2019        PMID: 31063232     DOI: 10.1002/kjm2.12085

Source DB:  PubMed          Journal:  Kaohsiung J Med Sci        ISSN: 1607-551X            Impact factor:   2.744


  16 in total

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Authors:  Junjie Wang; Jiangdong Ni; Deye Song; Muliang Ding; Jun Huang; Wenzhao Li; Guangxu He
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10.  Analysis of exosome-derived microRNAs reveals insights of intercellular communication during invasion of breast, prostate and glioblastoma cancer cells.

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Journal:  Cell Adh Migr       Date:  2021-12       Impact factor: 3.405

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