首页> 外文期刊>Biochemical Pharmacology >Indole-3-carbinol mediated cell cycle arrest of LNCaP human prostate cancer cells requires the induced production of activated p53 tumor suppressor protein.
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Indole-3-carbinol mediated cell cycle arrest of LNCaP human prostate cancer cells requires the induced production of activated p53 tumor suppressor protein.

机译:吲哚-3-甲醇介导的LNCaP人前列腺癌细胞的细胞周期停滞需要诱导产生活化的p53肿瘤抑制蛋白。

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Indole-3-carbinol (I3C), a dietary compound found naturally in cruciferous vegetables of the Brassica genus such as broccoli and brussels sprouts, induces a G1 growth arrest of human reproductive cancer cells. We previously reported that in LNCaP prostate cancer cells, I3C down-regulated cyclin-dependent kinase (CDK) 2 activity. In our current study, Western blotting and quantitative RT-PCR demonstrated that I3C treatment increased both the transcripts and protein levels of the CDK2 inhibitor p21(waf1/cip1) (p21). Transfection of luciferase reporter plasmids containing wild-type and mutated p21 promoter fragments revealed that I3C induced p21 gene transcription through a p53 DNA binding element. Oligonucleotide precipitation showed that I3C increased the level of activated p53 nuclear protein that is competent to bind its DNA target site on the p21 promoter. Ablation of p53 production using short interfering RNA (siRNA) prevented that the I3C induced G1 arrest and up-regulation of p21 expression. Western blots using p53 phospho-specific antibodies revealed that I3C treatment increased the levels of three phosphorylated forms of p53 (Ser15, Ser37, Ser392) that are known to contribute to p53 protein stability and greater transactivation potential. Taken together, our results establish that the I3C induced G1 arrest of human prostate cancer cells requires the induced production of the activated phosphorylated forms of p53, which stimulate transcription of the CDK2 inhibitor p21.
机译:吲哚-3-甲醇(I3C)是一种在芸苔属十字花科蔬菜(例如西兰花和抱子甘蓝)中天然发现的饮食化合物,可诱导人类生殖癌细胞的G1生长停滞。我们之前曾报道过,在LNCaP前列腺癌细胞中,I3C下调了细胞周期蛋白依赖性激酶(CDK)2的活性。在我们目前的研究中,蛋白质印迹和定量RT-PCR证明I3C处理可提高CDK2抑制剂p21(waf1 / cip1)(p21)的转录本和蛋白质水平。含有野生型和突变的p21启动子片段的萤光素酶报告质粒的转染表明,I3C通过p53 DNA结合元件诱导了p21基因的转录。寡核苷酸沉淀表明I3C增加了能结合p21启动子上其DNA靶位点的活化p53核蛋白的水平。使用短干扰RNA(siRNA)消融p53的产生可防止I3C诱导G1阻滞和p21表达的上调。使用p53磷酸特异性抗体的Western印迹显示,I3C处理提高了p53的三种磷酸化形式(Ser15,Ser37,Ser392)的水平,已知这三种形式有助于p53蛋白质的稳定性和更大的反式激活潜力。综上所述,我们的研究结果确定了I3C诱导的人前列腺癌细胞的G1阻滞需要诱导激活的磷酸化形式的p53的产生,从而刺激CDK2抑制剂p21的转录。

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