MicroRNAs: new players in the DNA damage response

被引:139
作者
Hu, Hailiang [1 ]
Gatti, Richard A. [1 ,2 ]
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, David Geffen Sch Med, Dept Human Genet, Los Angeles, CA 90095 USA
关键词
microRNA; DNA damage response; radiosensitivity; stem cells; CANCER STEM-CELLS; GENE-EXPRESSION; IONIZING-RADIATION; NUCLEAR EXPORT; P53; IDENTIFICATION; APOPTOSIS; TRANSCRIPTION; MODULATION; INDUCTION;
D O I
10.1093/jmcb/mjq042
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
The DNA damage response (DDR) is a signal transduction pathway that decides the cell's fate either to repair DNA damage or to undergo apoptosis if there is too much damage. Post-translational modifications modulate the assembly and activity of protein complexes during the DDR pathways. MicroRNAs (miRNAs) are emerging as a class of endogenous gene modulators that control protein levels, thereby adding a new layer of regulation to the DDR. In this review, we describe a new role for miRNAs in regulating the cellular response to DNA damage with a focus on DNA double-strand break damage. We also discuss the implications of miRNA's role in the DDR to stem cells, including embryonic stem cells and cancer stem cells, stressing the potential applications for miRNAs to be used as sensitizers for cancer radiotherapy and chemotherapy.
引用
收藏
页码:151 / 158
页数:8
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