Literature DB >> 10232953

Background DNA damage for endogenous and unavoidable exogenous carcinogens: a basis for spontaneous cancer incidence?

R C Gupta, W K Lutz.   

Abstract

It is undisputed today that DNA is constantly being damaged in the absence of any exposure to genotoxic carcinogens by a specific treatment or a particular habit. Damaging processes include endogenous and unavoidable exogenous sources. The list comprises chemical DNA instability (eg., depurination), spontaneous errors during DNA replication and repair, endogenous reactive chemicals (aldehydes, S-andenosylmethionine), numerous reactive oxygen species and products generated in consequence (e.g., lipid peroxides). Exogenous sources are ionizing and UV radiation, naturally occurring radioisotopes, and numerous genotoxic chemicals present in diet and air, both naturally or as contaminants. DNA repair and DNA replicative synthesis result in a constant reduction of the level of damage, but a certain steady-state level is measurable as a background at all times. The quantitative relationship between the background DNA damage and the spontaneous rates of mutation and cancer remains largely unknown. The quantitative relationship between the background DNA damange and the spontaneous rates of mutationa and caner remains largley unknown. In order to establish better correlations, more data have to be accumulated. This includes (i) measuring artefact-free levels of background DNA damage, (ii) investigating the mutagenic potency of the various lesions, (iii) including types of DNA damage other than adducts, and (iv) answer the question of organ-specific and cell type-specific +requirements for the primary DNA damage to be expressed as heritable genetic changes. The manuscripts put together for this Special Issue of Mutation Research describe the state of the art for these aspects. Copyright 1999 Elsevier Science B.V.

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Year:  1999        PMID: 10232953

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


  5 in total

1.  Endogenous oxidative DNA base modifications analysed with repair enzymes and GC/MS technique.

Authors:  P Jaruga; E Speina; D Gackowski; B Tudek; R Olinski
Journal:  Nucleic Acids Res       Date:  2000-03-15       Impact factor: 16.971

2.  Non-homologous end joining as an important mutagenic process in cell cycle-arrested cells.

Authors:  Erich Heidenreich; Rene Novotny; Bernd Kneidinger; Veronika Holzmann; Ulrike Wintersberger
Journal:  EMBO J       Date:  2003-05-01       Impact factor: 11.598

3.  ZNF365 promotes stalled replication forks recovery to maintain genome stability.

Authors:  Yuqing Zhang; Eunmi Park; Christopher S Kim; Ji-hye Paik
Journal:  Cell Cycle       Date:  2013-08-06       Impact factor: 4.534

Review 4.  Mode of action-based risk assessment of genotoxic carcinogens.

Authors:  Andrea Hartwig; Michael Arand; Bernd Epe; Sabine Guth; Gunnar Jahnke; Alfonso Lampen; Hans-Jörg Martus; Bernhard Monien; Ivonne M C M Rietjens; Simone Schmitz-Spanke; Gerlinde Schriever-Schwemmer; Pablo Steinberg; Gerhard Eisenbrand
Journal:  Arch Toxicol       Date:  2020-06-15       Impact factor: 5.153

Review 5.  What is the meaning of 'A compound is carcinogenic'?

Authors:  Dieter Schrenk
Journal:  Toxicol Rep       Date:  2018-04-07
  5 in total

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