| Literature DB >> 24076388 |
Lin Deng1, Yuanyuan Lu, Xiaodi Zhao, Yi Sun, Yongquan Shi, Hongwei Fan, Changhao Liu, Jinfeng Zhou, Yongzhan Nie, Kaichun Wu, Daiming Fan, Xuegang Guo.
Abstract
Ran, a member of the Ras GTPase family, has important roles in nucleocytoplasmic transport. Herein, we detected Ran expression in pancreatic cancer and explored its potential role on tumour progression. Overexpressed Ran in pancreatic cancer tissues was found highly correlated with the histological grade. Downregulation of Ran led to significant suppression of cell proliferation, cell cycle arrest at the G1/S phase and induction of apoptosis. In vivo studies also validated that result. Further studies revealed that those effects were at least partly mediated by the downregulation of Cyclin A, Cyclin D1, Cyclin E, CDK2, CDK4, phospho-Rb and Survivin proteins and up regulation of cleaved Caspase-3. CrownEntities:
Keywords: Cell cycle; Pancreatic cancer; Proliferation; Ran; Survivin
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Year: 2013 PMID: 24076388 DOI: 10.1016/j.bbrc.2013.09.079
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575