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首页> 外文期刊>The Prostate >Mxi1, a Myc antagonist, suppresses proliferation of DU145 human prostate cells.
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Mxi1, a Myc antagonist, suppresses proliferation of DU145 human prostate cells.

机译:Myc拮抗剂Mxi1抑制DU145人前列腺细胞的增殖。

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BACKGROUND: Mxi1, an antagonist of c-Myc, maps to human chromosome 10q24-q25, a region altered in a substantial fraction of prostate tumors. Mice deficient for Mxi1 exhibit significant prostate hyperplasia. We studied the ability of Mxi1 to act as a growth suppressor in prostate tumor cells. METHODS: We infected DU145 prostate carcinoma cells with an Mxi1-expressing adenovirus (AdMxi1) in vitro, and measured Mxi1 expression, cell proliferation, soft agar colony formation, and cell cycle distribution. To explore mechanisms of Mxi1-induced growth arrest, we performed gene expression analysis. RESULTS: AdMxi1 infection resulted in reduced cell proliferation, reduced soft agar colony formation, and a higher proportion of cells in the G(2)/M phase of the cell cycle. This G(2)/M growth arrest was associated with elevated levels of cyclin B, and reduced levels of c-MYC and MDM2. CONCLUSIONS: The ability of AdMxi1 to suppress prostate tumor cell proliferation supports a role for Mxi1 loss in the pathogenesis of a subset of human prostate cancers. Prostate 47:194-204, 2001. Copyright 2001 Wiley-Liss, Inc.
机译:背景:c-Myc的拮抗剂Mxi1定位到人类染色体10q24-q25,该区域在大部分前列腺肿瘤中都发生了改变。缺乏Mxi1的小鼠表现出明显的前列腺增生。我们研究了Mxi1在前列腺肿瘤细胞中充当生长抑制剂的能力。方法:我们在体外用表达Mxi1的腺病毒(AdMxi1)感染DU145前列腺癌细胞,并测量Mxi1表达,细胞增殖,软琼脂集落形成和细胞周期分布。为了探索Mxi1诱导的生长停滞的机制,我们进行了基因表达分析。结果:AdMxi1感染导致细胞增殖减少,软琼脂集落形成减少,并且在细胞周期的G(2)/ M期细胞比例更高。此G(2)/ M增长停滞与细胞周期蛋白B水平升高和c-MYC和MDM2水平降低相关。结论:AdMxi1抑制前列腺肿瘤细胞增殖的能力支持了Mxi1丢失在一部分人类前列腺癌的发病机理中的作用。前列腺47:194-204,2001。版权所有2001 Wiley-Liss,Inc.。

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