| Literature DB >> 28125315 |
Meng Wang1, Chuncheng Liu1, Yang Su1, Kuo Zhang1, Yuying Zhang1, Min Chen1, Mengxu Ge1, Lijie Gu1, Tianyu Lu1, Ning Li1, Zhengquan Yu1, Qingyong Meng1.
Abstract
miRNAs are increasingly being implicated as key regulators of cell proliferation, apoptosis, and differentiation. miRNA-34c appears to play a crucial role in cancer pathogenesis wherein it exerts its effect as a tumor suppressor. However, the role of miR-34c in myoblast proliferation remains poorly understood. Here, we found that overexpression miR-34c inhibited myoblasts proliferation by reducing the protein and mRNA expression of cell cycle genes. In contrast, blocking the function of miR-34c promoted myoblasts proliferation and increased the protein and mRNA expression of cell cycle genes. Moreover, miR-34c directly targeted YY1 and inhibited its expression. Similar to overexpression miR-34c, knockdown of YY1 by siRNA suppressed myoblasts proliferation. Our study provides novel evidence for a role of miR-34c in inhibiting myoblasts proliferation by repressing YY1. Thus, miR-34c has the potential to be used to enhance skeletal muscle development and regeneration.Entities:
Keywords: YY1; cell cycle; miR-34c; myoblast; proliferation
Mesh:
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Year: 2017 PMID: 28125315 PMCID: PMC5602293 DOI: 10.1080/15384101.2017.1281479
Source DB: PubMed Journal: Cell Cycle ISSN: 1551-4005 Impact factor: 4.534