| Literature DB >> 20423616 |
Xiang-E Long1, Zhao-Hui Gong, Lin Pan, Zhi-Wei Zhong, Yan-Ping Le, Qiong Liu, Jun-Ming Guo, Jiu-Chang Zhong.
Abstract
Cyclin-dependent kinase 2 (CDK2) is a member of serine/ threonine protein kinases, which initiates the principal transitions of the eukaryotic cell cycle and is a promising target for cancer therapy. The present study was designed to inhibit cdk2 gene expression to induce cell cycle arrest and cell proliferation suppression. Here, we constructed a series of RNA interference (RNAi) plasmids which can successfully express small interference RNA (siRNA) in the transfected human cells. The results showed that the RNAi plasmids containing the coding sequences for siRNAs down-regulated the cdk2 gene expression in human cancer cells at the mRNA and the protein levels. Furthermore, we found that the cell cycle was arrested at G0G1 phases and the cell proliferation was inhibited by different siRNAs. These results demonstrate that suppression of CDK2 activity by RNAi may be an effective strategy for gene therapy in human cancers.Entities:
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Year: 2010 PMID: 20423616 DOI: 10.5483/bmbrep.2010.43.4.291
Source DB: PubMed Journal: BMB Rep ISSN: 1976-6696 Impact factor: 4.778