The interplay between DNA repair and autophagy in cancer therapy

被引:110
作者
Zhang, Dan [1 ]
Tang, Bo [1 ]
Xie, Xia [1 ]
Xiao, Yu-Feng [1 ]
Yang, Shi-Ming [1 ]
Zhang, Jian-Wei [1 ]
机构
[1] Third Mil Med Univ, Xinqiao Hosp, Dept Gastroenterol, Chongqing, Peoples R China
关键词
anticancer therapy; autophagy; apoptosis; cell cycle arrest; DNA damage; DNA damage response; DNA repair; DOUBLE-STRAND BREAKS; NUCLEOTIDE EXCISION-REPAIR; DAMAGE RESPONSE; MOLECULAR-MECHANISMS; ANTICANCER COMPOUNDS; IONIZING-RADIATION; DRUG-RESISTANCE; MISMATCH REPAIR; MRN COMPLEX; HUMAN-CELLS;
D O I
10.1080/15384047.2015.1046022
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
DNA is the prime target of anticancer treatments. DNA damage triggers a series of signaling cascades promoting cellular survival, including DNA repair, cell cycle arrest, and autophagy. The elevated basal and/or stressful levels of both DNA repair and autophagy observed in tumor cells, in contrast to normal cells, have been identified as the most important drug-responsive programs that impact the outcome of anticancer therapy. The exact relationship between DNA repair and autophagy in cancer cells remains unclear. On one hand, autophagy has been shown to regulate some of the DNA repair proteins after DNA damage by maintaining the balance between their synthesis, stabilization, and degradation. One the other hand, some evidence has demonstrated that some DNA repair molecular have a crucial role in the initiation of autophagy. In this review, we mainly discuss the interplay between DNA repair and autophagy in anticancer therapy and expect to enlighten some effective strategies for cancer treatment.
引用
收藏
页码:1005 / 1013
页数:9
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