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The role of p53 and p21 on 8-chloro-adenosine-induced cellular response

机译:p53 和 p21 在 8-氯腺苷诱导的细胞反应中的作用

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8-Chloro-adenosine (8-Cl-Ado) is currently in phase I clinical trial. Activation of p53 and transactivation of p21 regulate cell fate after genotoxic insult. Using HCT-116-isogenic-cell-lines, we evaluated the role of p53/p21 after 8-Cl-Ado-mediated response. Following 30 mu M 8-Cl-Ado treatment, RNA synthesis was inhibited, p53 protein was stabilized, and p21 expression was activated. None of the cell types were arrested in G1/S phase, however, cells lacking p53 were blocked in G2/M. These cells had the least increase in apoptotic cells, although clonogenic survival demonstrated equal inhibition in all 4 cell types. Collectively, irrespective of p53 and p21 status, 8-Cl-Ado-induced cytotoxicity was similar.
机译:8-氯腺苷(8-Cl-Ado)目前处于I期临床试验阶段。p53 的激活和 p21 的反式激活调节遗传毒性损伤后的细胞命运。使用 HCT-116-isogenic-cell-lines,我们评估了 p53/p21 在 8-Cl-Ado 介导的反应后的作用。30 μ M 8-Cl-Ado处理后,抑制RNA合成,稳定p53蛋白,激活p21表达。所有细胞类型均未在G1/S期阻滞,但缺乏p53的细胞在G2/M期被阻断。这些细胞的凋亡细胞增加最少,尽管克隆形成存活在所有 4 种细胞类型中表现出相同的抑制作用。总的来说,无论 p53 和 p21 状态如何,8-Cl-Dodo 诱导的细胞毒性都是相似的。

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