首页> 外文期刊>Molecular Carcinogenesis >Induction of p53 and p21/WAF1/CIP1 expression by nitric oxide and their association with apoptosis in human cancer cells.
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Induction of p53 and p21/WAF1/CIP1 expression by nitric oxide and their association with apoptosis in human cancer cells.

机译:一氧化氮诱导p53和p21 / WAF1 / CIP1表达及其与人癌细胞凋亡的关系。

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In this study, human and rat cancer cells were used to investigate the expression of p53 and p21/WAF1/CIP1 and their association with apoptosis after exposure to nitric oxide (NO). It was found that NO induced nuclear accumulation of p53 protein in a dose- and time-dependent manner. The level of p53 protein was elevated by about fivefold compared with that of mock-treated cells 48 h after exposure to 300 ppm NO. The induction of p53 by NO was found by pulse-chase analysis to be mainly regulated by post-translational modification. The correlation between p53 status and apoptosis induced by NO in human cancer cells was also investigated in this study. We found that apoptosis was easily induced in cells containing wild-type p53 (COLO 205 and Hep G2) after exposure to NO. The p21/WAF1/CIP1 protein was induced by NO in cells containing wild-type p53 (Hep G2) but not in cells without p53 (Hep 3B) or with mutated p53 (HT-29). Our results indicate that wild-type p53 and p21/WAF1/CIP1 expression was elevated inhuman cancer cells by exposure to NO and suggest that this may eventually promote apoptosis.
机译:在这项研究中,人类和大鼠的癌细胞用于研究p53和p21 / WAF1 / CIP1的表达以及它们与一氧化氮(NO)接触后与凋亡的关系。发现NO以剂量和时间依赖性方式诱导p53蛋白的核积累。与暴露于300 ppm NO的模拟处理细胞相比,p53蛋白的水平与经过模拟处理的细胞相比,升高了约五倍。通过脉冲追踪分析发现NO对p53的诱导主要受翻译后修饰的调控。本研究还研究了p53状态与NO诱导人癌细胞凋亡的相关性。我们发现,暴露于NO后,含有野生型p53(COLO 205和Hep G2)的细胞容易诱导凋亡。 p21 / WAF1 / CIP1蛋白在含有野生型p53(Hep G2)的细胞中被NO诱导,但在没有p53(Hep 3B)或具有突变的p53(HT-29)的细胞中未被诱导。我们的结果表明,野生型p53和p21 / WAF1 / CIP1表达通过暴露于NO而在人癌细胞中升高,并表明这最终可能促进细胞凋亡。

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