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一个位于20号染色体q13区域的新型雄激素调节基因PMEPA1在前列腺中呈现高水平表达。

A novel androgen-regulated gene, PMEPA1, located on chromosome 20q13 exhibits high level expression in prostate.

作者信息

Xu L L, Shanmugam N, Segawa T, Sesterhenn I A, McLeod D G, Moul J W, Srivastava S

机构信息

Center for Prostate Disease Research, Uniformed Services University of the Health Sciences, Bethesda, Maryland, 20814-4799, USA.

出版信息

Genomics. 2000 Jun 15;66(3):257-63. doi: 10.1006/geno.2000.6214.

Abstract

Biologic effects of androgen on target cells are mediated in part by transcriptional regulation of androgen-regulated genes (ARGs) by androgen receptor. Using serial analysis of gene expression (SAGE), we have identified a comprehensive repertoire of ARGs in LNCaP cells. One of the SAGE-derived tags exhibiting homology to an expressed sequence tag was maximally induced in response to synthetic androgen R1881 treatment. The open reading frame of the androgen-induced RNA (PMEPA1) was characterized as a 759-bp nucleotide sequence coding for a 252-amino-acid protein. The analysis of PMEPA1 protein sequence indicated the existence of a type Ib transmembrane domain between residues 9 and 25. Analysis of multiple-tissue Northern blots revealed the highest level of PMEPA1 expression in prostate tissue. PMEPA1 expression was predominately detected in glandular epithelial cells of prostate by in situ hybridization analysis. The expression of PMEPA1 in LNCaP cells was induced by androgen in a time- and dose-specific manner. Evaluation of PMEPA1 expression in androgen-dependent/independent tumors of the CWR22 xenograft model revealed that PMEPA1 was overexpressed in three of four androgen-independent tumor tissues. These observations define PMEPA1 as a novel androgen-regulated gene exhibiting abundant expression in prostate tissue. The increased expression of PMEPA1 in relapsed tumors of the CWR22 model suggests activation of androgen signaling in hormone refractory disease. PMEPA1, along with other highly androgen-induced prostate-specific genes, has potential to serve as an androgen signaling read-out biomarker in prostate tissue.

摘要

雄激素对靶细胞的生物学效应部分是由雄激素受体对雄激素调节基因(ARGs)的转录调控介导的。通过基因表达系列分析(SAGE),我们已经在LNCaP细胞中鉴定出了ARGs的完整目录。其中一个与表达序列标签具有同源性的SAGE衍生标签在合成雄激素R1881处理后被最大程度地诱导。雄激素诱导的RNA(PMEPA1)的开放阅读框被鉴定为一个759个碱基对的核苷酸序列,编码一个252个氨基酸的蛋白质。对PMEPA1蛋白序列的分析表明,在第9和25位氨基酸残基之间存在一个Ib型跨膜结构域。对多组织Northern印迹的分析显示,PMEPA1在前列腺组织中的表达水平最高。原位杂交分析显示,PMEPA1主要在前列腺的腺上皮细胞中表达。雄激素以时间和剂量特异性的方式诱导LNCaP细胞中PMEPA1的表达。对CWR22异种移植模型的雄激素依赖性/非依赖性肿瘤中PMEPA1表达的评估显示,在四个雄激素非依赖性肿瘤组织中的三个中,PMEPA1过表达。这些观察结果将PMEPA1定义为一种在前列腺组织中大量表达的新型雄激素调节基因。CWR22模型复发性肿瘤中PMEPA1表达的增加表明在激素难治性疾病中雄激素信号通路被激活。PMEPA1与其他高度雄激素诱导的前列腺特异性基因一起,有可能作为前列腺组织中雄激素信号读出生物标志物。

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