ROS and the DNA damage response in cancer

被引:1383
作者
Srinivas, Upadhyayula Sai [1 ]
Tan, Bryce W. Q. [1 ]
Vellayappan, Balamurugan A. [2 ]
Jeyasekharan, Anand D. [1 ,3 ]
机构
[1] Natl Univ Singapore, Canc Sci Inst Singapore, Singapore, Singapore
[2] Natl Univ Singapore Hosp, Dept Radiat Oncol, Singapore, Singapore
[3] Natl Univ Singapore Hosp, Dept Haematol Oncol, Singapore, Singapore
来源
REDOX BIOLOGY | 2019年 / 25卷
基金
英国医学研究理事会; 新加坡国家研究基金会;
关键词
Reactive Oxygen Species; ROS; DNA damage response; DDR; Chemotherapy; Radiotherapy; HISTONE H2AX PHOSPHORYLATION; CHECKPOINT KINASE INHIBITOR; OXYGEN SPECIES PRODUCTION; OXIDATIVE STRESS; MOTEXAFIN-GADOLINIUM; GENOMIC INSTABILITY; CDC25; PHOSPHATASES; THERAPEUTIC TARGET; REDOX REGULATION; CELL CARCINOMA;
D O I
10.1016/j.redox.2018.101084
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Reactive oxygen species (ROS) are a group of short-lived, highly reactive, oxygen-containing molecules that can induce DNA damage and affect the DNA damage response (DDR). There is unequivocal pre-clinical and clinical evidence that ROS influence the genotoxic stress caused by chemotherapeutics agents and ionizing radiation. Recent studies have provided mechanistic insight into how ROS can also influence the cellular response to DNA damage caused by genotoxic therapy, especially in the context of Double Strand Breaks (DSBs). This has led to the clinical evaluation of agents modulating ROS in combination with genotoxic therapy for cancer, with mixed success so far. These studies point to context dependent outcomes with ROS modulator combinations with Chemotherapy and radiotherapy, indicating a need for additional pre-clinical research in the field. In this review, we discuss the current knowledge on the effect of ROS in the DNA damage response, and its clinical relevance.
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页数:9
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