| Literature DB >> 25152372 |
Zhenguo Cheng1, Funan Liu2, Guanqiao Wang1, Yanshu Li1, Hongyan Zhang1, Feng Li3.
Abstract
Cell division cycle 42 (CDC42), an important member of the Ras homolog (Rho) family, plays a key role in regulating multiple cellular processes such as cell cycle progression, migration, cell cytoskeleton organization, cell fate determination and differentiation. Among the downstream effectors of CDC42, P21-activated kinases (PAKs) obtain the most attention. Although a large body of evidence indicates that CDC42/PAKs pathway plays important role in tumor growth, invasion and metastasis, the mechanism of their negative regulation remains unclear. Here, we identified CDC42, a PAKs activating factor, was a target of miR-133. Ectopic overexpression of miRNAs not only downregulated CDC42 expression and PAKs activation, but also inhibited cancer cell proliferation and migration. We also found that miR-133 was down-regulated in 180 pairs gastric cancer tissues. miR-133 expression was negatively associated with tumor size, invasion depth and peripheral organ metastasis. Besides, dysfunction of miR-133 was an independent prognosis factor for overall survival. Our findings could provide new insights into the molecular mechanisms of gastric carcinogenesis, and may help facilitating development of CDC42/PAK-based therapies for human cancer.Entities:
Keywords: Activation; CDC42; Gastric cancer; Invasion; miR-133; p21-activated kinase
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Year: 2014 PMID: 25152372 DOI: 10.1016/j.cellsig.2014.08.012
Source DB: PubMed Journal: Cell Signal ISSN: 0898-6568 Impact factor: 4.315