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共济失调毛细血管扩张症及Rad3相关蛋白与DNA依赖性蛋白激酶在DNA链断裂核苷类似物2'-C-氰基-2'-脱氧-1-β-D-阿拉伯呋喃糖基胞嘧啶激活G2期检查点过程中协同发挥作用。

Ataxia-telangiectasia and Rad3-related and DNA-dependent protein kinase cooperate in G2 checkpoint activation by the DNA strand-breaking nucleoside analogue 2'-C-cyano-2'-deoxy-1-beta-D-arabino-pentofuranosylcytosine.

作者信息

Liu Xiaojun, Matsuda Akira, Plunkett William

机构信息

Department of Experimental Therapeutics, The University of Texas M. D. Anderson Cancer Center, Box 71, 1515 Holcombe Boulevard, Houston, TX 77030, USA.

出版信息

Mol Cancer Ther. 2008 Jan;7(1):133-42. doi: 10.1158/1535-7163.MCT-07-0416.

Abstract

2'-C-cyano-2'-deoxy-1-beta-D-arabino-pentofuranosylcytosine (CNDAC), the prodrug (sapacitabine) of which is in clinical trials, has the novel mechanism of action of causing single-strand breaks after incorporating into DNA. Cells respond to this unique lesion by activating the G2 checkpoint, affected by the Chk1-Cdc25C-cyclin-dependent kinase 1/cyclin B pathway. This study aims at defining DNA damage checkpoint sensors that activate this response to CNDAC, particularly focusing on the major phosphatidylinositol 3-kinase-like protein kinase family proteins. First, fibroblasts, deficient in ataxia-telangiectasia mutated (ATM), transfected with empty vector or repleted with ATM, were arrested in G2 by CNDAC to similar extents, suggesting ATM is not required to activate the G2 checkpoint. Second, chromatin associations of RPA70 and RPA32, subunits of the ssDNA-binding protein, and the ataxia-telangiectasia and Rad3-related (ATR) substrate Rad17 and its phosphorylated form were increased on CNDAC exposure, suggesting activation of ATR kinase. The G2 checkpoint was abrogated due to depletion of ATR by small interfering RNA, and impaired in ATR-Seckel cells, indicating participation of ATR in this G2 checkpoint pathway. Third, the G2 checkpoint was more stringent in glioma cells with wild-type DNA-dependent protein kinase catalytic subunit (DNA-PKcs) than those with mutant DNA-PKcs, as shown by mitotic index counting. CNDAC-induced G2 arrest was abrogated by specific DNA-PKcs inhibitors or small interfering RNA knockdown in ML-1 and/or HeLa cells. Finally, two phosphatidylinositol 3-kinase-like protein kinase inhibitors, caffeine and wortmannin, abolished the CNDAC-induced G2 checkpoint in a spectrum of cell lines. Together, our data showed that ATR and DNA-PK cooperate in CNDAC-induced activation of the G2 checkpoint pathway.

摘要

2'-C-氰基-2'-脱氧-1-β-D-阿拉伯呋喃糖基胞嘧啶(CNDAC),其前药(沙帕他滨)正在进行临床试验,具有在掺入DNA后导致单链断裂的新型作用机制。细胞通过激活受Chk1-Cdc25C-细胞周期蛋白依赖性激酶1/细胞周期蛋白B途径影响的G2检查点来应对这种独特的损伤。本研究旨在确定激活对CNDAC这种反应的DNA损伤检查点传感器,特别关注主要的磷脂酰肌醇3-激酶样蛋白激酶家族蛋白。首先,用空载体转染或补充有共济失调毛细血管扩张症突变(ATM)的共济失调毛细血管扩张症突变(ATM)缺陷成纤维细胞,被CNDAC在G2期阻滞到相似程度,表明激活G2检查点不需要ATM。其次,单链DNA结合蛋白的亚基RPA70和RPA32以及共济失调毛细血管扩张症和Rad3相关(ATR)底物Rad17及其磷酸化形式的染色质结合在暴露于CNDAC时增加,表明ATR激酶被激活。由于小干扰RNA使ATR耗竭,G2检查点被废除,并且在ATR-塞克尔细胞中受损,表明ATR参与了该G2检查点途径。第三,如通过有丝分裂指数计数所示,具有野生型DNA依赖性蛋白激酶催化亚基(DNA-PKcs)的胶质瘤细胞中的G2检查点比具有突变型DNA-PKcs的胶质瘤细胞更严格。在ML-1和/或HeLa细胞中,特异性DNA-PKcs抑制剂或小干扰RNA敲低消除了CNDAC诱导的G2阻滞。最后,两种磷脂酰肌醇3-激酶样蛋白激酶抑制剂咖啡因和渥曼青霉素在一系列细胞系中消除了CNDAC诱导的G2检查点。总之,我们的数据表明ATR和DNA-PK在CNDAC诱导的G2检查点途径激活中协同作用。

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