Suppr超能文献

利用 RNAi 表型筛选鉴定调控前列腺癌细胞生长的激酶。

Identification of kinases regulating prostate cancer cell growth using an RNAi phenotypic screen.

机构信息

Department of Microbiology, University of Virginia, Charlottesville, Virginia, United States of America.

出版信息

PLoS One. 2012;7(6):e38950. doi: 10.1371/journal.pone.0038950. Epub 2012 Jun 27.

Abstract

As prostate cancer progresses to castration-resistant disease, there is an increase in signal transduction activity. Most castration-resistant prostate tumors continue to express the androgen receptor (AR) as well as androgen-responsive genes, despite the near absence of circulating androgen in these patients. The AR is regulated not only by its cognate steroid hormone, but also by interactions with a constellation of co-regulatory and signaling molecules. Thus, the elevated signaling activity that occurs during progression to castration resistance can affect prostate cancer cell growth either through the AR or independent of the AR. In order to identify signaling pathways that regulate prostate cancer cell growth, we screened a panel of shRNAs targeting 673 human kinases against LNCaP prostate cancer cells grown in the presence and absence of hormone. The screen identified multiple shRNA clones against known and novel gene targets that regulate prostate cancer cell growth. Based on the magnitude of effect on growth, we selected six kinases for further study: MAP3K11, DGKD, ICK, CIT, GALK2, and PSKH1. Knockdown of these kinases decreased cell growth in both androgen-dependent and castration-resistant prostate cancer cells. However, these kinases had different effects on basal or androgen-induced transcriptional activity of AR target genes. MAP3K11 knockdown most consistently altered transcription of AR target genes, suggesting that MAP3K11 affected its growth inhibitory effect by modulating the AR transcriptional program. Consistent with MAP3K11 acting on the AR, knockdown of MAP3K11 inhibited AR Ser 650 phosphorylation, further supporting stress kinase regulation of AR phosphorylation. This study demonstrates the applicability of lentiviral-based shRNA for conducting phenotypic screens and identifies MAP3K11, DGKD, ICK, CIT, GALK2, and PSKH1 as regulators of prostate cancer cell growth. The thorough evaluation of these kinase targets will pave the way for developing more effective treatments for castration-resistant prostate cancer.

摘要

随着前列腺癌进展为去势抵抗性疾病,信号转导活性增加。尽管这些患者的循环雄激素几乎不存在,但大多数去势抵抗性前列腺肿瘤仍继续表达雄激素受体(AR)和雄激素反应基因。AR 的调节不仅受其同源甾体激素的调节,还受一系列共调节和信号分子的相互作用的调节。因此,在进展为去势抵抗时发生的升高的信号转导活性可以通过 AR 或独立于 AR 影响前列腺癌细胞的生长。为了鉴定调节前列腺癌细胞生长的信号通路,我们针对在存在和不存在激素的情况下生长的 LNCaP 前列腺癌细胞,筛选了针对 673 个人类激酶的 shRNA 文库。该筛选确定了针对调节前列腺癌细胞生长的已知和新基因靶标的多个 shRNA 克隆。基于对生长的影响程度,我们选择了六种激酶进行进一步研究:MAP3K11、DGKD、ICK、CIT、GALK2 和 PSKH1。这些激酶的敲低降低了雄激素依赖性和去势抵抗性前列腺癌细胞的细胞生长。然而,这些激酶对 AR 靶基因的基础或雄激素诱导的转录活性有不同的影响。MAP3K11 的敲低最一致地改变了 AR 靶基因的转录,这表明 MAP3K11 通过调节 AR 转录程序影响其生长抑制作用。与 MAP3K11 作用于 AR 一致,MAP3K11 的敲低抑制了 AR Ser 650 磷酸化,进一步支持应激激酶调节 AR 磷酸化。这项研究证明了基于慢病毒的 shRNA 进行表型筛选的适用性,并确定了 MAP3K11、DGKD、ICK、CIT、GALK2 和 PSKH1 是前列腺癌细胞生长的调节剂。对这些激酶靶标的全面评估将为开发更有效的去势抵抗性前列腺癌治疗方法铺平道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e1b/3384611/d017086fb62e/pone.0038950.g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验