生物
雄激素受体
前列腺癌
基因沉默
LNCaP公司
抑制因子
融合蛋白
转录因子
癌症研究
基因
核受体
遗传学
癌症
重组DNA
作者
Joanna Pike,David Holmes,Tahereh Kamalati,Derek Davies,Robert S. Tolhurst,Danish Mazhar,Sam Fishpool,Rajai Al-Jehani,Jonathan Waxman,Arthur Zelent,Nicholas R. Lemoine,Simak Ali,Laki Buluwela
出处
期刊:Oncogene
[Springer Nature]
日期:2004-08-30
卷期号:23 (45): 7561-7570
被引量:10
标识
DOI:10.1038/sj.onc.1208030
摘要
The androgen receptor (AR) is a member of the nuclear receptor superfamily of ligand-activated transcription factors and plays a key role in the development and progression of prostate cancer. Current therapies include the use of antiandrogens aimed at inhibiting the transcriptional activation of AR-regulated genes by AR. Here, we explore a strategy aimed at obtaining silencing of AR-regulated genes, based on the properties of the transcriptional repressor promyelocytic leukamia zinc-finger protein (PLZF). In order to do this, we have made a fusion protein between PLZF and AR, named PLZF-AR, and show that PLZF-AR is able to bring about silencing of genomically encoded AR-regulated genes and inhibit the androgen-regulated growth of LNCaP prostate cancer cells. Together, our results show that this strategy is able to bring about potent repression of AR-regulated responses and, therefore, could be of value in the development of new therapies for prostate cancer.
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