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Inhibition of p53 Protein Phosphorylation by 9‐Hydroxyellipticine: A Possible Anticancer Mechanism

机译:9-羟基玫瑰树碱抑制p53蛋白磷酸化:可能的抗癌机制。

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摘要

Abnormality of p53, a tumor suppressor gene, is considered to be a potential cause of malignancy. We found that ellipticine and 9‐hydroxyellipticine (9HE), antitumor alkaloids, caused selective inhibition of p53 protein phospborylation in Lewis lung carcinoma and SW480 (human colon cancer cell line) in a concentration‐dependent manner from 0.1 to 100 μM. 9HE suppressed cdk2 kinase activity concentration‐dependently from 1 to 100 μM. By contrast, the inhibition of p53 protein phosphorylation by elliptinium and elliprabin (N2 substituted derivatives of 9HE) was very weak. A good correlation was observed between p53 phosphorylation inhibition and cytotoxic activity of these agents in terms of concentration‐response relationships, suggesting that inhibition of p53 protein phosphorylation via kinase inhibition may be involved in the anticancer mechanism of these agents. In addition, this study demonstrated that brief exposure to 9HE caused apoptosis of cancer cells. It is suggested that accumulation of dephosphorylated mutant p53 may induce apoptosis.
机译:p53(一种抑癌基因)的异常被认为是导致恶性肿瘤的潜在原因。我们发现玫瑰树碱和9-羟基玫瑰树碱(9HE)是抗肿瘤生物碱,以0.1至100μM的浓度依赖性方式选择性抑制Lewis肺癌和SW480(人结肠癌细胞系)中p53蛋白的磷酸化。 9HE抑制cdk2激酶活性浓度从1到100μM依赖性。相比之下,椭圆形和椭圆形蛋白(9HE的N2取代衍生物)对p53蛋白磷酸化的抑制作用非常弱。就浓度-反应关系而言,在这些药物的p53磷酸化抑制与细胞毒性活性之间观察到良好的相关性,这表明通过激酶抑制对p53蛋白磷酸化的抑制可能与这些药物的抗癌机制有关。此外,这项研究表明,短暂暴露于9HE会导致癌细胞凋亡。提示去磷酸化的突变体p53的积累可能诱导细胞凋亡。

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