...
首页> 外文期刊>Cell Division >Damaged-DNA Binding Protein-2 Drives Apoptosis Following DNA Damage
【24h】

Damaged-DNA Binding Protein-2 Drives Apoptosis Following DNA Damage

机译:DNA损伤后,DNA结合蛋白2驱动细胞凋亡。

获取原文
           

摘要

Apoptosis induced by DNA damage is an important mechanism of tumor suppression and it is significant also in cancer chemotherapy. Mammalian cells activate the pathways of p53 to induce apoptosis of cells harboring irreparable DNA damages. While p53 induces expression of various pro-apoptotic genes and directly participates in the disruption of mitochondrial membrane polarization, it also increases expression of the cell cycle inhibitor p21 that is a dominant inhibitor of caspase-activation and apoptosis. Here we discuss how Damaged-DNA Binding Protein-2 (DDB2) subdues the level of p21 in cells harboring irreparable DNA damage to support activation of the caspases. We speculate a model in which DDB2 detects and couples the presence of un-repaired DNA damages to the proteolysis of p21, leading to the induction of apoptosis.
机译:DNA损伤诱导的细胞凋亡是抑制肿瘤的重要机制,在癌症化疗中也很重要。哺乳动物细胞激活p53的通路,诱导具有不可修复的DNA损伤的细胞凋亡。虽然p53诱导各种促凋亡基因的表达并直接参与线粒体膜极化的破坏,但它也增加了细胞周期抑制剂p21的表达,后者是caspase激活和凋亡的主要抑制剂。在这里,我们讨论受损DNA结合蛋白2(DDB2)如何抑制细胞中p21的水平,该细胞具有不可修复的DNA损伤以支持胱天蛋白酶的激活。我们推测一个模型,其中DDB2检测并耦合未修复的DNA损伤的存在对p21的蛋白水解,导致细胞凋亡的诱导。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号