Identification of CDK2 as a novel target in treatment of prostate cancer

细胞周期蛋白依赖激酶2 基因 生物 前列腺癌 转移 癌症研究 计算生物学 癌症 遗传学 细胞周期
作者
Xifeng Yin,Jun Yu,Yang Zhou,Chengyue Wang,Zhimin Jiao,Zhounan Qian,Hao Sun,Binghai Chen
出处
期刊:Future Oncology [Future Medicine]
卷期号:14 (8): 709-718 被引量:43
标识
DOI:10.2217/fon-2017-0561
摘要

This study aims the potential gene involved in the metastasis of prostate cancer (Pca).PubMed GEO datasets (GSE6605 and GSE6606) were downloaded. We used multiple bioinformatics methods to screen differentially expressed genes in Pca. Gene network was built by STRING and visualized by Cytoscape. All of the hub genes were analyzed by cBioPortal. Inhibition of CDK2 including siRNA, inhibitor and cas9-induced CDK2 knockout was followed by an invasion assay. Downstream genes of CDK2 were analyzed by western blot.Sequencing data were analyzed to screen the genes with expression alterations. The top genes were validated in our samples. 11 hub genes were screened out. Among these genes, STAT3 and CDK2 were significantly associated with recurrence. Further study suggested that inhibition of CDK2 reduced invasion of Pca cell lines. The invasion ability was rescued after reintroduction of CDK2.These data indicated that CDK2 was a crucial factor in metastasis of Pca and might be a novel therapy target. [Formula: see text].

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