MicroRNAs and DNA damage response Implications for cancer therapy

被引:81
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
相关论文
共 150 条
[71]   A double-strand break repair defect in ATM-deficient cells contributes to radiosensitivity [J].
Kühne, M ;
Riballo, E ;
Rief, N ;
Rothkamm, K ;
Jeggo, PA ;
Löbrich, M .
CANCER RESEARCH, 2004, 64 (02) :500-508
[72]   Negative regulation of the tumor suppressor p53 gene by microRNAs [J].
Kumar, M. ;
Lu, Z. ;
Takwi, A. A. L. ;
Chen, W. ;
Callander, N. S. ;
Ramos, K. S. ;
Young, K. H. ;
Li, Y. .
ONCOGENE, 2011, 30 (07) :843-853
[73]   miR-24 Inhibits Cell Proliferation by Targeting E2F2, MYC, and Other Cell-Cycle Genes via Binding to "Seedless" 3′UTR MicroRNA Recognition Elements [J].
Lal, Ashish ;
Navarro, Francisco ;
Maher, Christopher A. ;
Maliszewski, Laura E. ;
Yan, Nan ;
O'Day, Elizabeth ;
Chowdhury, Dipanjan ;
Dykxhoorn, Derek M. ;
Tsai, Perry ;
Hofmann, Oliver ;
Becker, Kevin G. ;
Gorospe, Myriam ;
Hide, Winston ;
Lieberman, Judy .
MOLECULAR CELL, 2009, 35 (05) :610-625
[74]   miR-24-mediated downregulation of H2AX suppresses DNA repair in terminally differentiated blood cells [J].
Lal, Ashish ;
Pan, Yunfeng ;
Navarro, Francisco ;
Dykxhoorn, Derek M. ;
Moreau, Lisa ;
Meire, Eti ;
Bentwich, Zvi ;
Lieberman, Judy ;
Chowdhury, Dipanjan .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2009, 16 (05) :492-498
[75]   MicroRNAs in Mutagenesis, Genomic Instability, and DNA Repair [J].
Landau, Dan-Avi ;
Slack, Frank J. .
SEMINARS IN ONCOLOGY, 2011, 38 (06) :743-751
[76]   MicroRNA-125b is a novel negative regulator of p53 [J].
Le, Minh T. N. ;
Teh, Cathleen ;
Shyh-Chang, Ng ;
Xie, Huangming ;
Zhou, Beiyan ;
Korzh, Vladimir ;
Lodish, Harvey F. ;
Lim, Bing .
GENES & DEVELOPMENT, 2009, 23 (07) :862-876
[77]   Regulation of the p27Kip1 tumor suppressor by miR-221 and miR-222 promotes cancer cell proliferation [J].
le Sage, Carlos ;
Nagel, Remco ;
Egan, David A. ;
Schrier, Mariette ;
Mesman, Elly ;
Mangiola, Annunziato ;
Anile, Corrado ;
Maira, Giulio ;
Mercatelli, Neri ;
Ciafre, Silvia Anna ;
Farace, Maria Giulia ;
Agami, Reuven .
EMBO JOURNAL, 2007, 26 (15) :3699-3708
[78]  
Lee H, 2012, NAT NANOTECHNOL, V7, P389, DOI [10.1038/nnano.2012.73, 10.1038/NNANO.2012.73]
[79]   let-7 Overexpression Leads to an Increased Fraction of Cells in G2/M, Direct Down-regulation of Cdc34, and Stabilization of Wee1 Kinase in Primary Fibroblasts [J].
Legesse-Miller, Aster ;
Elemento, Olivier ;
Pfau, Sarah J. ;
Forman, Joshua J. ;
Tavazoie, Saeed ;
Coller, Hilary A. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2009, 284 (11) :6605-6609
[80]   Emerging common themes in regulation of PIKKs and PI3Ks [J].
Lempiaeinen, Harri ;
Halazonetis, Thanos D. .
EMBO JOURNAL, 2009, 28 (20) :3067-3073