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The MDM2-inhibitor Nutlin-3 synergizes with cisplatin to induce p53 dependent tumor cell apoptosis in non-small cell lung cancer

机译:mDm2抑制剂Nutlin-3与顺铂协同诱导非小细胞肺癌p53依赖性肿瘤细胞凋亡

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摘要

The p53/MDM2 interaction has been a well-studied target for new drug design leading to the development of the small molecule inhibitor Nutlin-3. Our objectives were to combine Nutlin-3 with cisplatin (CDDP), a well-known activator of the p53 pathway, in a series of non-small cell lung cancer cell lines in order to increase the cytotoxic response to CDDP. We report that sequential treatment (CDDP followed by Nutlin-3), but not simultaneous treatment, resulted in strong synergism. Combination treatment induced p53's transcriptional activity, resulting in increased mRNA and protein levels of MDM2, p21, PUMA and BAX. In addition we report the induction of a strong p53 dependent apoptotic response and induction of G2/M cell cycle arrest. The strongest synergistic effect was observed at low doses of both CDDP and Nutlin-3, which could result in fewer (off-target) side effects while maintaining a strong cytotoxic effect. Our results indicate a promising preclinical potential, emphasizing the importance of the applied treatment scheme and the presence of wild type p53 for the combination of CDDP and Nutlin-3.
机译:p53 / MDM2相互作用一直是导致开发小分子抑制剂Nutlin-3的新药设计的充分研究的目标。我们的目标是在一系列非小细胞肺癌细胞系中将Nutlin-3与顺铂(CD53)(一种著名的p53途径激活剂)结合,以增强对CDDP的细胞毒性反应。我们报告说,顺序治疗(CDDP后接Nutlin-3),而不是同时治疗,导致强烈的协同作用。联合治疗诱导p53的转录活性,导致MDM2,p21,PUMA和BAX的mRNA和蛋白水平增加。此外,我们报告了诱导强烈的p53依赖性凋亡反应和诱导G2 / M细胞周期停滞。在低剂量的CDDP和Nutlin-3上观察到最强的协同作用,这可能导致较少的(脱靶)副作用,同时保持强大的细胞毒性作用。我们的结果表明了有希望的临床前潜力,强调了所应用治疗方案的重要性以及CDDP和Nutlin-3组合存在野生型p53的重要性。

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