MicroRNAs and DNA damage response Implications for cancer therapy

被引:80
|
作者
Wang, Yemin
Taniguchi, Toshiyasu [1 ]
机构
[1] Fred Hutchinson Canc Res Ctr, Howard Hughes Med Inst, Seattle, WA 98104 USA
关键词
microRNA; DNA damage response; DNA repair; chemotherapy; radiotherapy; DNA damaging agents; TUMOR-SUPPRESSOR P53; STRAND BREAK REPAIR; MUTS HOMOLOG 2; CELL-CYCLE; IONIZING-RADIATION; DOWN-REGULATION; PROCESSING PATHWAY; NEGATIVE REGULATION; PRECURSOR MICRORNA; MISMATCH REPAIR;
D O I
10.4161/cc.23051
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The DNA damage response (DDR) pathways play critical roles in protecting the genome from DNA damage. Abrogation of DDR often results in elevated genomic instability and cellular sensitivity to DNA damaging agents. Many proteins involved in DDR are subjected to precise regulation at multiple levels, such as transcriptional control and posttranslational modifications, in response to DNA damage. MicroRNAs (miRNAs) are a class of small non-coding RNAs that negatively regulate gene expression at the post-transcriptional level. The expression levels of some miRNAs change in response to DNA damage. Some miRNAs, such as miR-24, 138, 96 and 182, have been implicated in DDR and/or DNA repair and affect cellular sensitivity to DNA damaging agents. In this review, we summarize recent findings related to the emerging roles of miRNAs in regulating DDR and DNA repair and discuss their potential in cancer therapy.
引用
收藏
页码:32 / 42
页数:11
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