Visconti Roberta, Della Monica Rosa, Grieco Domenico
IEOS, CNR, Via S. Pansini 5, 80131, Naples, Italy.
DMMBM, University of Naples "Federico II", Via S. Pansini 5, 80131, Naples, Italy.
J Exp Clin Cancer Res. 2016 Sep 27;35(1):153. doi: 10.1186/s13046-016-0433-9.
Major currently used anticancer therapeutics either directly damage DNA or target and upset basic cell division mechanisms like DNA replication and chromosome segregation. These insults elicit activation of cell cycle checkpoints, safeguard mechanisms that cells implement to correctly complete cell cycle phases, repair damage or eventually commit suicide in case damage is unrepairable. Although cancer cells appear to be advantageously defective in some aspects of checkpoint physiology, recent acquisitions on the biochemical mechanisms of the various checkpoints are offering new therapeutic approaches against cancer. Indeed, chemical manipulation of these mechanisms is providing new therapeutic strategies and tools to increase the killing efficacy of major cancer therapeutics as well as to directly promote cancer cell death. In this review we summarize developing concepts on how targeting cell cycle checkpoints may provide substantial improvement to cancer therapy.
目前主要使用的抗癌疗法要么直接损伤DNA,要么靶向并扰乱DNA复制和染色体分离等基本细胞分裂机制。这些损伤会引发细胞周期检查点的激活,细胞通过这些保障机制来正确完成细胞周期阶段、修复损伤,或者在损伤无法修复时最终自我毁灭。尽管癌细胞在检查点生理学的某些方面似乎存在有利的缺陷,但最近对各种检查点生化机制的研究为抗癌提供了新的治疗方法。事实上,对这些机制的化学调控正在提供新的治疗策略和工具,以提高主要癌症疗法的杀伤效果,并直接促进癌细胞死亡。在这篇综述中,我们总结了关于靶向细胞周期检查点如何能显著改善癌症治疗的最新概念。