Redox Environment, Free Radical, and Oxidative DNA Damage

被引:87
作者
Storr, Sarah J. [1 ]
Woolston, Caroline M. [1 ]
Zhang, Yimin [1 ]
Martin, Stewart G. [1 ]
机构
[1] Univ Nottingham, Nottingham Univ Hosp Trust, Sch Mol Med Sci, Nottingham NG5 1PB, England
关键词
BASE-EXCISION-REPAIR; HUMAN AP ENDONUCLEASE-1; HUMAN 8-OXOGUANINE-DNA GLYCOSYLASE; HOGG1 SER326CYS POLYMORPHISM; UP-REGULATED PROTEIN-1; SUPEROXIDE-DISMUTASE; CELL-GROWTH; FACTOR-I; APURINIC/APYRIMIDINIC ENDONUCLEASE; POLY(ADP-RIBOSE) POLYMERASE;
D O I
10.1089/ars.2012.4920
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Significance: Effective redox homeostasis is critical, and disruption of this process can have important cellular consequences. An array of systems protect the cell from potentially damaging reactive oxygen species (ROS), however if these systems are overwhelmed, for example, in aberrantly functioning cells, ROS can have a number of detrimental consequences, including DNA damage. Oxidative DNA damage can be repaired by a number of DNA repair pathways, such as base excision repair (BER). Recent Advances: The role of ROS in oxidative DNA damage is well established, however, there is an emerging role for ROS and the redox environment in modulating the efficiency of DNA repair pathways targeting oxidative DNA lesions. Critical Issues: Oxidative DNA damage and modulation of DNA damage and repair by the redox environment are implicated in a number of diseases. Understanding how the redox environment plays such a critical role in DNA damage and repair will allow us to further understand the far reaching cellular consequence of ROS. Future Directions: In this review, we discuss the detrimental effects of ROS, oxidative DNA damage repair, and the redox systems that exist to control redox homeostasis. We also describe how DNA pathways can be modulated by the redox environment and how the redox environment and oxidative DNA damage plays a role in disease.
引用
收藏
页码:2399 / 2408
页数:10
相关论文
共 117 条
[1]   ATM signals to TSC2 in the cytoplasm to regulate mTORC1 in response to ROS [J].
Alexander, Angela ;
Cai, Sheng-Li ;
Kim, Jinhee ;
Nanez, Adrian ;
Sahin, Mustafa ;
MacLean, Kirsteen H. ;
Inoki, Ken ;
Guan, Kun-Liang ;
Shen, Jianjun ;
Person, Maria D. ;
Kusewitt, Donna ;
Mills, Gordon B. ;
Kastan, Michael B. ;
Walker, Cheryl Lyn .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2010, 107 (09) :4153-4158
[2]   Kinetic analysis of the Ku-DNA binding activity reveals a redox-dependent alteration in protein structure that stimulates dissociation of the Ku-DNA complex [J].
Andrews, BJ ;
Lehman, JA ;
Turchi, JJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (19) :13596-13603
[3]   Molecular Mechanisms of Thioredoxin and Glutaredoxin as Hydrogen Donors for Mammalian S Phase Ribonucleotide Reductase [J].
Avval, Farnaz Zahedi ;
Holmgren, Arne .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2009, 284 (13) :8233-8240
[4]   Mutation in the glucose-6-phosphate dehydrogenase gene leads to inactivation of Ku DNA end binding during oxidative stress [J].
Ayene, IS ;
Stamato, TD ;
Mauldin, SK ;
Biaglow, JE ;
Tuttle, SW ;
Jenkins, SF ;
Koch, CJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (12) :9929-9935
[5]   BRCA1 induces antioxidant gene expression and resistance to oxidative stress [J].
Bae, I ;
Fan, S ;
Meng, QH ;
Rih, JK ;
Kim, HJ ;
Kang, HJ ;
Xu, JW ;
Goldberg, ID ;
Jaiswal, AK ;
Rosen, EM .
CANCER RESEARCH, 2004, 64 (21) :7893-7909
[6]   Molecular analysis of Ku redox regulation [J].
Bennett, Sara M. ;
Neher, Tracy M. ;
Shatilla, Andrea ;
Turchi, John J. .
BMC MOLECULAR BIOLOGY, 2009, 10 :86
[7]   Acetylation of human 8-oxoguanine-DNA glycosylase by p300 and its role in 8-oxoguanine repair in vivo [J].
Bhakat, KK ;
Mokkapati, SK ;
Boldogh, I ;
Hazra, TK ;
Mitra, S .
MOLECULAR AND CELLULAR BIOLOGY, 2006, 26 (05) :1654-1665
[8]   Redox regulation of human OGG1 activity in response to cellular oxidative stress [J].
Bravard, Anne ;
Vacher, Monique ;
Gouget, Barbara ;
Coutant, Alexandre ;
de Boisferon, Florence Hillairet ;
Marsin, Stephanie ;
Chevillard, Sylvie ;
Radicella, J. Pablo .
MOLECULAR AND CELLULAR BIOLOGY, 2006, 26 (20) :7430-7436
[9]   Oxidation Status of Human OGG1-S326C Polymorphic Variant Determines Cellular DNA Repair Capacity [J].
Bravard, Anne ;
Vacher, Monique ;
Moritz, Eva ;
Vaslin, Laurence ;
Hall, Janet ;
Epe, Bernd ;
Radicella, J. Pablo .
CANCER RESEARCH, 2009, 69 (08) :3642-3649
[10]   Structural basis for recognition and repair of the endogenous mutagen 8-oxoguanine in DNA [J].
Bruner, SD ;
Norman, DPG ;
Verdine, GL .
NATURE, 2000, 403 (6772) :859-866