| Literature DB >> 29068476 |
Xin Jin1, Zhiliang Zhang1, Yi Lu1, Zhihong Fan1.
Abstract
Long non coding RNAs (lncRNAs) show an encouraging trend in regulating the proliferation of bone marrow-derived mesenchymal stromal cells (BMSCs). The present study investigated the role of lncRNA low expression in tumor (LET) in BMSCs proliferation. Our result showed that LET was down-regulated in rapidly proliferated BMSCs (P < 0.05). Suppression of LET promoted BMSCs proliferation and over-expression of LET inhibited BMSCs proliferation (P < 0.05). LET negatively regulated the expression of transforming growth factor β1 (TGF-β1) in BMSCs (P < 0.05). Knockdown of TGF-β1 reversed the LET suppression-induced BMSCs proliferation (P < 0.05). Moreover, knockdown of TGF-β1 alleviated the LET suppression-induced activation of Wnt/β-catenin pathway in BMSCs. Therefore, we drew the conclusion that LET suppression promoted BMSCs proliferation by up-regulating the expression of TGF-β1 and activating Wnt/β-catenin pathway.Entities:
Keywords: Cell proliferation; LncRNA low expression in tumor; Wnt/β-catenin pathway; bone marrow stem cells; transforming growth factor β1
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Year: 2017 PMID： 29068476 DOI： 10.1002/jcb.26459
Source DB: PubMed Journal: J Cell Biochem ISSN： 0730-2312 Impact factor: 4.429