The DNA Damage Response-Repair or Despair?

被引:36
作者
Ljungman, Mats [1 ,2 ]
机构
[1] Univ Michigan, Dept Radiat Oncol, Ctr Comprehens Canc, Div Radiat & Canc Biol, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Sch Publ Hlth, Dept Environm Hlth Sci, Ann Arbor, MI 48109 USA
关键词
DNA repair; cell cycle checkpoints; apoptosis; aging; review; cancer; NUCLEOTIDE EXCISION-REPAIR; LIGHT-INDUCED APOPTOSIS; DOUBLE-STRAND BREAKS; MONOCHROMATIC ULTRAVIOLET-RADIATION; TRANSCRIPTION-COUPLED REPAIR; CELL-CYCLE REGULATION; LI-FRAUMENI SYNDROME; RNA-POLYMERASE-II; XERODERMA-PIGMENTOSUM; ESCHERICHIA-COLI;
D O I
10.1002/em.20597
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The term "the DNA damage response" (DDR) encompasses a sophisticated array of cellular initiatives set in motion as cells are exposed to DNA-damaging events. It has been known for over half a century that all organisms have the ability to restore genomic integrity through DNA repair. More recent discoveries of signal transduction pathways linking DNA damage to cell cycle arrest and apoptosis have greatly expanded our views of how cells and tissues limit mutagenesis and tumorigenesis. DNA repair not only plays a pivotal role in suppressing mutagenesis but also in the reversal of signals inducing the stress response. If repair is faulty or the cell is overwhelmed by damage, chances are that the cell will despair and be removed by apoptosis. This final fate is determined by intricate cellular dosimeters that are yet to be fully understood. Here, key findings leading to our current view of DDR are discussed as well as potential areas of importance for future studies. Environ. Mol. Mutagen. 51:879-889, 2010. (c) 2010 Wiley-Liss, Inc.
引用
收藏
页码:879 / 889
页数:11
相关论文
共 131 条
[61]   Radiation-induced gene translation profiles reveal tumor type and cancer-specific components [J].
Kumaraswamy, Sandhya ;
Chinnaiyan, Prakash ;
Shankavaram, Uma T. ;
Lue, Xing ;
Camphausen, Kevin ;
Tofilon, Philip J. .
CANCER RESEARCH, 2008, 68 (10) :3819-3826
[62]   p38 Mitogen-Activated Protein Kinase- and HuR-Dependent Stabilization of p21Cip1 mRNA Mediates the G1/S Checkpoint [J].
Lafarga, Vanesa ;
Cuadrado, Ana ;
Lopez de Silanes, Isabel ;
Bengoechea, Rocio ;
Fernandez-Capetillo, Oscar ;
Nebreda, Angel R. .
MOLECULAR AND CELLULAR BIOLOGY, 2009, 29 (16) :4341-4351
[63]   Posttranscriptional derepression of GADD45α by genotoxic stress [J].
Lal, A ;
Abdelmohsen, K ;
Pullmann, R ;
Kawai, T ;
Galban, S ;
Yang, XL ;
Brewer, G ;
Gorospe, M .
MOLECULAR CELL, 2006, 22 (01) :117-128
[64]   T-ANTIGEN IS BOUND TO A HOST PROTEIN IN SV40-TRANSFORMED CELLS [J].
LANE, DP ;
CRAWFORD, LV .
NATURE, 1979, 278 (5701) :261-263
[65]   N-GLYCOSIDASE FROM ESCHERICHIA-COLI THAT RELEASES FREE URACIL FROM DNA CONTAINING DEAMINATED CYTOSINE RESIDUES [J].
LINDAHL, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1974, 71 (09) :3649-3653
[66]   CHARACTERIZATION OF A 54K DALTON CELLULAR SV40 TUMOR-ANTIGEN PRESENT IN SV40-TRANSFORMED CELLS AND UNINFECTED EMBRYONAL CARCINOMA-CELLS [J].
LINZER, DIH ;
LEVINE, AJ .
CELL, 1979, 17 (01) :43-52
[67]   LOCALIZED TORSIONAL TENSION IN THE DNA OF HUMAN-CELLS [J].
LJUNGMAN, M ;
HANAWALT, PC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (13) :6055-6059
[68]   Induction of ser15 and lys382 modifications of p53 by blockage of transcription elongation [J].
Ljungman, M ;
O'Hagan, HM ;
Paulsen, MT .
ONCOGENE, 2001, 20 (42) :5964-5971
[69]  
Ljungman M, 1996, ONCOGENE, V13, P823
[70]   Activation of DNA damage signaling [J].
Ljungman, M .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2005, 577 (1-2) :203-216