Chen Bin, Wen Pengbo, Hu Guanshuo, Gao Yang, Qi Xiaojing, Zhu Kaili, Chen Shaopeng, Wu Lijun, Xu An, Zhao Guoping
Key Laboratory of High Magnetic Field and Ion Beam Physical Biology, Anhui Province Key Laboratory of Environmental Toxicology and Pollution Control Technology, Hefei Institutes of Physical Science, Chinese Academy of Sciences, Hefei, China.
University of Science and Technology of China, Hefei, China.
Front Cell Dev Biol. 2020 Jun 12;8:408. doi: 10.3389/fcell.2020.00408. eCollection 2020.
Radiotherapy is an essential curative treatment modality for colorectal cancer. Apoptosis is the major mechanism of IR-induced cell death and aberrant apoptotic signaling results in radioresistance, which is a hallmark of most, perhaps all, types of human cancers. Potentiating the induction of apoptosis is an emerging strategy for cancer radiotherapy. Here, we determined that targeting CDK8 selectively radiosensitized colorectal cancer through the mitochondria-dependent intrinsic apoptotic signaling, which was mediated through the induction of the transcription of apaf1 that was e2f1- and not p53-dependent. Importantly, the enhanced transcriptional activity of e2f1 was dependent on the kinase activity of CDK8 itself and not on the assembling of the mediator complex. In addition, clinical inhibitor, and studies confirmed the radiosensitizing effect of CDK8. Our results provide a new targeting strategy to improve the radiotherapy of CRC.
放射治疗是结直肠癌的一种重要的根治性治疗方式。细胞凋亡是电离辐射诱导细胞死亡的主要机制,而异常的凋亡信号传导会导致放射抗性,这是大多数(或许是所有)人类癌症类型的一个标志。增强细胞凋亡的诱导是癌症放射治疗中一种新兴的策略。在此,我们确定通过线粒体依赖性内源性凋亡信号传导选择性地靶向细胞周期蛋白依赖性激酶8(CDK8)可使结直肠癌对放疗敏感,该信号传导是由e2f1而非p53依赖性诱导凋亡蛋白酶激活因子1(apaf1)的转录介导的。重要的是,e2f1增强的转录活性依赖于CDK8自身的激酶活性,而不依赖于中介复合物的组装。此外,临床抑制剂研究证实了CDK8的放射增敏作用。我们的结果为改善结直肠癌的放疗提供了一种新的靶向策略。