Literature DB >> 18083609

Mechanism of oxidative DNA damage repair and relevance to human pathology.

Mariarosaria D'Errico1, Eleonora Parlanti, Eugenia Dogliotti.   

Abstract

Since DNA is prone to oxidative attack cells have evolved multiple protective strategies to prevent the deleterious effects of DNA oxidation. Base excision repair is the major mechanism for repair of DNA base damage by reactive oxygen species but recent evidence indicate that nucleotide excision repair proteins, that are mutated in human syndromes, are involved too. The mechanisms of repair dealing with the direct oxidation of DNA will be reviewed taking as prototype the oxidized base 7,8-dihydro-8-hydroxyguanine. The function of the individual repair components as inferred from model mice indicate that the ablation of two gene functions is mostly required to lead to accumulation of oxidative DNA damage, mutagenesis and cancer development. The recent identification of human diseases associated with mutations in oxidative damage repair show that defects in this pathway may lead to increased cancer but their major causative role seems to be in neurological diseases.

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Year:  2007        PMID: 18083609     DOI: 10.1016/j.mrrev.2007.10.003

Source DB:  PubMed          Journal:  Mutat Res        ISSN: 0027-5107            Impact factor:   2.433


  29 in total

Review 1.  Base excision repair and lesion-dependent subpathways for repair of oxidative DNA damage.

Authors:  David Svilar; Eva M Goellner; Karen H Almeida; Robert W Sobol
Journal:  Antioxid Redox Signal       Date:  2010-10-28       Impact factor: 8.401

2.  The polymerase eta translesion synthesis DNA polymerase acts independently of the mismatch repair system to limit mutagenesis caused by 7,8-dihydro-8-oxoguanine in yeast.

Authors:  Sarah V Mudrak; Caroline Welz-Voegele; Sue Jinks-Robertson
Journal:  Mol Cell Biol       Date:  2009-07-27       Impact factor: 4.272

Review 3.  DNA damage and autophagy.

Authors:  Humberto Rodriguez-Rocha; Aracely Garcia-Garcia; Mihalis I Panayiotidis; Rodrigo Franco
Journal:  Mutat Res       Date:  2011-03-17       Impact factor: 2.433

Review 4.  Back to the future: transgenerational transmission of xenobiotic-induced epigenetic remodeling.

Authors:  Josep C Jiménez-Chillarón; Mark J Nijland; António A Ascensão; Vilma A Sardão; José Magalhães; Michael J Hitchler; Frederick E Domann; Paulo J Oliveira
Journal:  Epigenetics       Date:  2015-03-16       Impact factor: 4.528

Review 5.  Modulation of mutagenesis in eukaryotes by DNA replication fork dynamics and quality of nucleotide pools.

Authors:  Irina S-R Waisertreiger; Victoria G Liston; Miriam R Menezes; Hyun-Min Kim; Kirill S Lobachev; Elena I Stepchenkova; Tahir H Tahirov; Igor B Rogozin; Youri I Pavlov
Journal:  Environ Mol Mutagen       Date:  2012-10-10       Impact factor: 3.216

6.  Silencing of RB1 but not of RB2/P130 induces cellular senescence and impairs the differentiation potential of human mesenchymal stem cells.

Authors:  Nicola Alessio; Wolfgang Bohn; Verena Rauchberger; Flavio Rizzolio; Marilena Cipollaro; Michael Rosemann; Martin Irmler; Johannes Beckers; Antonio Giordano; Umberto Galderisi
Journal:  Cell Mol Life Sci       Date:  2013-01-31       Impact factor: 9.261

7.  8-Oxo-7,8-dihydroguanine: links to gene expression, aging, and defense against oxidative stress.

Authors:  Zsolt Radak; Istvan Boldogh
Journal:  Free Radic Biol Med       Date:  2010-05-17       Impact factor: 7.376

8.  Unlike catalyzing error-free bypass of 8-oxodGuo, DNA polymerase λ is responsible for a significant part of Fapy·dG-induced G → T mutations in human cells.

Authors:  Paritosh Pande; Kazuhiro Haraguchi; Yu-Lin Jiang; Marc M Greenberg; Ashis K Basu
Journal:  Biochemistry       Date:  2015-03-06       Impact factor: 3.162

9.  Toward consensus in the analysis of urinary 8-oxo-7,8-dihydro-2'-deoxyguanosine as a noninvasive biomarker of oxidative stress.

Authors:  Mark D Evans; Ryszard Olinski; Steffen Loft; Marcus S Cooke
Journal:  FASEB J       Date:  2009-12-04       Impact factor: 5.191

10.  Pristanic acid provokes lipid, protein, and DNA oxidative damage and reduces the antioxidant defenses in cerebellum of young rats.

Authors:  Estela Natacha Brandt Busanello; Vannessa Gonçalves Araujo Lobato; Ângela Zanatta; Clarissa Günther Borges; Anelise Miotti Tonin; Carolina Maso Viegas; Vanusa Manfredini; César Augusto João Ribeiro; Carmen Regla Vargas; Diogo Onofre Gomes de Souza; Moacir Wajner
Journal:  Cerebellum       Date:  2014-12       Impact factor: 3.847

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