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Identification and characterization of the novel human prostate cancer-specific PC-1 gene promoter

机译:新型人类前列腺癌特异性PC-1基因启动子的鉴定与表征

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Human prostate and colon gene-1 (PC-1, also known as PrLZ) is an androgen-regulated, prostate tissue and prostate cancer cells specifically expressed novel gene. The increased expression of PC-1 gene appears to promote prostate cancer cells androgen-dependent (AD) and androgen-independent (AI) growth. To clone and investigate the expression and regulation elements of PC-1 gene may provide insight into the function of PC-1 and develop a new promoter that targets therapeutic genes to the AD and AI prostate cancer cells. The goal of the present study is cloning and characterization of the PC-1 promoter. A series of luciferase constructs that contain various fragments of the PC-1 5'-genomic region were transfected into human prostate cancer cells for promoter transactivation analysis. 5' deletion analysis identified the -1579 bp promoter region was required for the maximal proximal promoter activity; two transcriptional suppression and a positive regulatory region were identified; -4939 bp promoter fragment of the PC-1 gene retained the characteristic of prostate cancer-specific expression and exhibited higher transcription activity than PSA-6 kb promoter in the medium supplemented with steroid-depleted FBS. An androgen response element (ARE) was located in between -345 and -359 bp of the PC-1 5'-untranslated region relative to the translation initiation site. Thus, our studies not only provide molecular basis of PC-1 transcription regulation, but also define a new regulatory sequence that may be used to restrict expression of therapeutic genes to prostate cancer in the prostate cancer gene therapy. (c) 2007 Elsevier Inc. All rights reserved.
机译:人前列腺和结肠基因1(PC-1,也称为PrLZ)是一种雄激素调节的前列腺组织和前列腺癌细胞,专门表达新基因。 PC-1基因表达的增加似乎促进了前列腺癌细胞的雄激素依赖性(AD)和雄激素依赖性(AI)生长。克隆和研究PC-1基因的表达和调控元件可能提供对PC-1功能的洞察力,并开发出将治疗基因靶向AD和AI前列腺癌细胞的新启动子。本研究的目的是克隆和表征PC-1启动子。将一系列包含PC-1 5'基因组区域各种片段的荧光素酶构建体转染到人前列腺癌细胞中,以进行启动子反式激活分析。 5'缺失分析确定了最大近端启动子活性需要-1579 bp启动子区域;确定了两个转录抑制和一个正调控区。 PC-1基因的-4939 bp启动子片段保留了前列腺癌特异性表达的特征,并且在补充类固醇缺乏的FBS的培养基中表现出比PSA-6 kb启动子更高的转录活性。相对于翻译起始位点,雄激素应答元件(ARE)位于PC-1 5'非翻译区的-345至-359 bp之间。因此,我们的研究不仅提供了PC-1转录调控的分子基础,而且定义了一种新的调控序列,可用于在前列腺癌基因治疗中将治疗基因的表达限制在前列腺癌中。 (c)2007 Elsevier Inc.保留所有权利。

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