Suppr超能文献

NKX-3.1与前列腺源性Ets因子相互作用并调节前列腺特异性抗原(PSA)启动子的活性。

NKX-3.1 interacts with prostate-derived Ets factor and regulates the activity of the PSA promoter.

作者信息

Chen Hui, Nandi Asit K, Li Xiang, Bieberich Charles J

机构信息

Department of Biological Sciences, University of Maryland, Baltimore County, Baltimore, Maryland 21250, USA.

出版信息

Cancer Res. 2002 Jan 15;62(2):338-40.

Abstract

The NKX-3.1 homeobox gene maps to human chromosome 8p21, a region that undergoes frequent loss of heterozygosity in prostate tumors. Loss of Nkx-3.1 function in mice leads to epithelial overgrowth. To further elucidate the molecular basis of NKX-3.1 function, a genetic screen for proteins that interact with NKX-3.1 was performed. Prostate-derived Ets factor (PDEF) was identified as a potential partner of NKX-3.1. Coimmunoprecipitation analyses demonstrated that NKX-3.1 and PDEF are physically associated in prostate epithelial cells. Cotransfection analyses demonstrated that NKX-3.1 can abolish the transcriptional activation function of PDEF on the prostate-specific antigen (PSA) promoter. These data identify PSA as a target gene for NKX-3.1 and provide new insights into the function of this candidate tumor suppressor.

摘要

NKX-3.1 同源框基因定位于人类染色体 8p21,该区域在前列腺肿瘤中经常发生杂合性缺失。小鼠中 Nkx-3.1 功能的丧失会导致上皮过度生长。为了进一步阐明 NKX-3.1 功能的分子基础,进行了与 NKX-3.1 相互作用蛋白质的遗传筛选。前列腺衍生的 Ets 因子(PDEF)被鉴定为 NKX-3.1 的潜在伙伴。免疫共沉淀分析表明,NKX-3.1 和 PDEF 在前列腺上皮细胞中存在物理关联。共转染分析表明,NKX-3.1 可以消除 PDEF 对前列腺特异性抗原(PSA)启动子的转录激活功能。这些数据确定 PSA 为 NKX-3.1 的靶基因,并为这种候选肿瘤抑制因子 的功能提供了新见解。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验