| Literature DB >> 24333727 |
Gui-Jun Yan1, Fei Yu2, Bin Wang1, Huai-Jun Zhou3, Qiu-Yan Ge1, Jing Su1, Ya-Li Hu1, Hai-Xiang Sun4, Li-Jun Ding5.
Abstract
MicroRNA miR-302 has been found to induce some tumor cell lines to "transdifferentiate" into miRNA-induced pluripotent stem cells (mirPS), thereby inhibiting tumor cell proliferation and reducing tumorigenicity. This study firstly found that miR-302 inhibited the proliferation and migration of endometrial cell line, Ishikawa and HEC-1-B, and arrested cell cycle at the G2/M phase. In addition, miR-302 inhibited tumorigenicity in immunodeficient mice transplanted with Ishikawa cells. Microarray and Western blotting results showed that miR-302 significantly inhibited CDK1 and Cyclin D1 gene expression in Ishikawa cells. MiR-302 directly targeted Cyclin D1, but indirectly regulated CDK1 gene expression.Entities:
Keywords: G2/M phase; HEC-1-B cells; Ishikawa cells; MicroRNA miR-302
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Year: 2013 PMID: 24333727 DOI: 10.1016/j.canlet.2013.11.023
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679