| Literature DB >> 30076753 |
Liang Yan1,2, Meng-Chao Yu1, Guang-Lei Gao3, Hong-Wei Liang1, Xin-Yan Zhou1, Zhou-Ting Zhu4, Chen-Yu Zhang1, Ya-Bing Wang5, Xi Chen1.
Abstract
MicroRNAs (miRNAs) play an important role in the regulation of human cancers, including breast cancer (BC). In the current study, we examined the expression pattern of the miRNA miR-125a-5p in human BC tissues, tumorigenesis of BC progression. We found that miR-125a-5p was significantly downregulated in human BC tissues. Overexpression of miR-125a-5p in a xenograft mouse model indicated that miR-125a-5p may function as a tumour suppressor during carcinogenesis. To explore the molecular mechanism by which miR-125a-5p contributes to BC progression, we predicted the target genes of miR-125a-5p and identified BC susceptibility gene 1-associated protein 1 (BAP1) as a direct target. Finally, we demonstrated that BAP1 had opposing effects to those of miR-125a-5p on BC cells, suggesting that miR-125a-5p may inhibit cell proliferation and promote cell apoptosis by negatively regulating BAP1. Taken together, our findings provide the first clues regarding the role of miR-125a-5p as a tumour suppressor in BC via the inhibition of BAP1 translation.Entities:
Keywords: BAP1; breast cancer; miR-125a-5p
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Year: 2018 PMID: 30076753 DOI: 10.1002/jcb.27124
Source DB: PubMed Journal: J Cell Biochem ISSN: 0730-2312 Impact factor: 4.429