首页> 外文期刊>Oncogenesis. >MicroRNA-29a regulates the benzo[a]pyrene dihydrodiol epoxide-induced DNA damage response through Cdc7 kinase in lung cancer cells

摘要

Cdc7 kinase is a key regulator of DNA replication and has an important role in the cellular DNA damage response by controlling checkpoint signaling and cell survival. Yet, how the activity of Cdc7 kinase is regulated is poorly understood. In silico analysis identified microRNA-29 (miR-29)-binding sites in the 3′-untranslated region (UTR) of both Cdc7 and its activating subunit Dbf4. We show that miR-29a binds to Cdc7 and Dbf4 3′-UTRs and regulates kinase levels. We find that in response to DNA damage, upregulation of Cdc7 kinase correlates with a downregulation in miR-29a. Enforced miR-29a expression prevents the accumulation of Cdc7 in response to the environmental genotoxin, benzo[ a ]pyrene dihydrodiol epoxide (BPDE) present in cigarette smoke, resulting in aberrant checkpoint signaling and increased cell lethality. As BPDE sensitivity was rescued by overexpression of miRNA-resistant Cdc7/Dbf4, we propose that Cdc7 kinase is an important target of miR-29a in determining cell survival from genotoxic stress caused by this environmental toxin.
机译:Cdc7激酶是DNA复制的关键调节剂,并通过控制检查点信号传导和细胞存活在细胞DNA损伤反应中发挥重要作用。但是,人们对Cdc7激酶活性的调控方式知之甚少。在计算机分析中确定了Cdc7及其激活亚基Dbf4的3'-非翻译区(UTR)中的microRNA-29(miR-29)结合位点。我们显示,miR-29a与Cdc7和Dbf4 3'-UTRs结合并调节激酶水平。我们发现,响应DNA损伤,Cdc7激酶的上调与miR-29a的下调相关。增强的miR-29a表达可防止Cdc7积累,以响应香烟烟气中存在的环境基因毒素,苯并[a] py二氢二醇环氧化物(BPDE),从而导致异常的检查点信号传递和增加的细胞杀伤力。由于通过抗miRNA的Cdc7 / Dbf4的过量表达挽救了BPDE敏感性,因此我们建议Cdc7激酶是miR-29a的重要靶标,它可以确定这种环境毒素导致的遗传毒性应激中的细胞存活。

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