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PMID: 22289176 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Cyclin-dependent kinase 4 is a novel target in micoRNA-195-mediated cell cycle arrest in bladder cancer cells.

FEBS letters ·Vol. 586 ·No. 4 ·2012-02-17 ·Pages 442-7

Lin Y, Wu J, Chen H, Mao Y, Liu Y, Mao Q, Yang K, Zheng X, Xie L

Abstract

miRNAs are a class of small-noncoding RNAs capable of negatively regulating gene expression. Here, we found that miR-195 is down-regulated in human bladder cancer tissue versus normal adjacent tissue. To better characterize the role of miR-195 in bladder cancer, we conducted gain of function analysis by transfecting bladder cancer cell line T24 with chemically synthesized miR-195 mimic. We identified CDK4, an early G1 cell cycle regulator, as a novel target of miR-195. Selective over-expression of miR-195 could induce G1-phase arrest in T24 cells, and subsequently inhibit T24 cell growth. These findings indicate that miR-195 could be a potential tumor suppressor in bladder cancer.

MeSH Terms
Base Sequence Cell Cycle Checkpoints/genetics,physiology Cell Line, Tumor Cell Proliferation Cyclin-Dependent Kinase 4/genetics,metabolism Down-Regulation G1 Phase Humans MicroRNAs/genetics RNA, Neoplasm/genetics Tumor Stem Cell Assay Urinary Bladder Neoplasms/genetics,metabolism,pathology
Chemicals
MIRN195 microRNA, human MicroRNAs RNA, Neoplasm CDK4 protein, human Cyclin-Dependent Kinase 4
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Lin Yiwei
Department of Urology, The First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, Zhejiang Province, China.
Wu Jian
Chen Hong
Mao Yeqing
Liu Yunfu
Mao Qiqi
Yang Kai
Zheng Xiangyi
Xie Liping
Article Info
Journal
FEBS letters
Abbr.
FEBS Lett
ISSN
1873-3468
Published
2012-02-17
Epub
2012-00-28
Pages
442-7
Language
English
Region
England
NLM ID
0155157
Subset
IM
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