Icilin inhibits E2F1-mediated cell cycle regulatory programs in prostate cancer

被引:18
|
作者
Lee, Sanghoon [1 ]
Chun, Jung Nyeo [2 ,3 ]
Kim, Su-Hwa [2 ]
So, Insuk [2 ,3 ]
Jeon, Ju-Hong [2 ,3 ]
机构
[1] Univ Utah, Sch Med, Dept Biochem, Salt Lake City, UT 84112 USA
[2] Seoul Natl Univ, Coll Med, Dept Physiol & Biomed Sci, Seoul 110799, South Korea
[3] Seoul Natl Univ, Inst Human Environm Interface Biol, Seoul 110799, South Korea
基金
新加坡国家研究基金会;
关键词
Bioinformatics; Microarray; Gene expression profiling; Icilin; Prostate cancer; ANDROGEN-RECEPTOR; E2F1; ARREST; SELECTION; NETWORKS; KINASE; GROWTH; GENES;
D O I
10.1016/j.bbrc.2013.11.015
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Aberrant expression of cell cycle regulators have been implicated in prostate cancer development and progression. Therefore, understanding transcriptional networks controlling the cell cycle remain a challenge in the development of prostate cancer treatment. In this study, we found that icilin, a super-cooling agent, down-regulated the expression of cell cycle signature genes and caused G(1) arrest in PC-3 prostate cancer cells. With reverse-engineering and an unbiased interrogation of a prostate cancer-specific regulatory network, master regulator analysis discovered that icilin affected cell cycle-related transcriptional modules and identified E2F1 transcription factor as a target master regulator of icilin. Experimental analyses confirmed that icilin reduced the activity and expression levels of E2F1. These results demonstrated that icilin inactivates a small regulatory module controlling the cell cycle in prostate cancer cells. Our study might provide insight into the development of cell cycle-targeted cancer therapeutics. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:1005 / 1010
页数:6
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