miR-140-5p inhibits the proliferation and enhances the efficacy of doxorubicin to breast cancer stem cells by targeting Wnt1

被引:0
|
作者
Dawei Wu
Jun Zhang
Ying Lu
Song Bo
Lianhong Li
Lu Wang
Qingqing Zhang
Jun Mao
机构
[1] The Second Hospital of Tianjian Medical University,Department of Clinical Laboratory
[2] Dalian Medical University,Department of Pathology
[3] Dalian Medical University,Teaching Laboratory of Morphology
[4] Dalian Medical University,Key Laboratory of Tumor Stem Cell Research of Liaoning Province
来源
Cancer Gene Therapy | 2019年 / 26卷
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摘要
MicroRNAs (miRNAs) are a group of small non-coding single-stranded RNAs molecules, the dysregulation of which plays a critical role in the initiation and biological progression of malignancies. The current study demonstrated that miR-140-5p was frequently downregulated in breast cancer stem cells (BCSCs), and miR-140-5p mimics could inhibit the proliferation of BCSCs. Moreover, Wnt1 was a direct target of miR-140-5p, as was proved by luciferase reporter assays. miR-140-5p mimics could downregulate the wnt1 mRNA and protein levels in MCF-7 and MDA-MB-231 cells. Furthermore, miR-140 mimics could enhance the sensitivity of BCSCs to doxorubicin (Dox) through the Wnt1/ABCB1 pathway both in vitro and vivo. Our findings have presented a novel miRNA-mediated regulatory network for BCSCs, which may provide a potential therapeutic target for breast cancer.
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页码:74 / 82
页数:8
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