Literature DB >> 8013423

DNA lesions, inducible DNA repair, and cell division: three key factors in mutagenesis and carcinogenesis.

B N Ames1, M K Shigenaga, L S Gold.   

Abstract

DNA lesions that escape repair have a certain probability of giving rise to mutations when the cell divides. Endogenous DNA damage is high: 10(6) oxidative lesions are present per rat cell. An exogenous mutagen produces an increment in lesions over the background rate of endogenous lesions. The effectiveness of a particular lesion depends on whether it is excised by a DNA repair system and the probability that it gives rise to a mutation when the cell divides. When the cell divides, an unrepaired DNA lesion has a certain probability of giving rise to a mutation. Thus, an important factor in the mutagenic effect of an exogenous agent whether it is genotoxic or non-genotoxic, is the increment it causes over the background cell division rate (mitogenesis) in cells that appear to matter most in cancer, the stem cells, which are not on their way to being discarded. Increasing their cell division rate increases mutation and therefore cancer. There is little cancer from nondividing cells. Endogenous cell division rates can be influenced by hormone levels, decreased by calorie restriction, or increased by high doses of chemicals. If both the rate of DNA lesions and cell division are increased, then there will be a multiplicative effect on mutagenesis (and carcinogenesis), for example, by high doses of a mutagen that also increases mitogenesis through cell killing. The defense system against reactive electrophilic mutagens, such as the glutathione transferases, are also almost all inducible and buffer cells against increments in active forms of chemicals that can cause DNA lesions. A variety of DNA repair defense systems, almost all inducible, buffer the cell against any increment in DNA lesions. Therefore, the effect of a particular chemical insult depends on the level of each defense, which in turn depends on the past history of exposure. Exogenous agents can influence the induction and effectiveness of these defenses. Defenses can be partially disabled by lack of particular micronutrients in the diet (e.g., antioxidants).

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Year:  1993        PMID: 8013423      PMCID: PMC1519422          DOI: 10.1289/ehp.93101s535

Source DB:  PubMed          Journal:  Environ Health Perspect        ISSN: 0091-6765            Impact factor:   9.031


  136 in total

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Review 3.  The inheritance of epigenetic defects.

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Authors:  R Holliday
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6.  Urinary 8-hydroxy-2'-deoxyguanosine as a biological marker of in vivo oxidative DNA damage.

Authors:  M K Shigenaga; C J Gimeno; B N Ames
Journal:  Proc Natl Acad Sci U S A       Date:  1989-12       Impact factor: 11.205

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8.  Ascorbic acid protects against endogenous oxidative DNA damage in human sperm.

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9.  Two adjacent AP-1-like binding sites form the electrophile-responsive element of the murine glutathione S-transferase Ya subunit gene.

Authors:  R S Friling; S Bergelson; V Daniel
Journal:  Proc Natl Acad Sci U S A       Date:  1992-01-15       Impact factor: 11.205

10.  Second chronological supplement to the Carcinogenic Potency Database: standardized results of animal bioassays published through December 1984 and by the National Toxicology Program through May 1986.

Authors:  L S Gold; T H Slone; G M Backman; R Magaw; M Da Costa; P Lopipero; M Blumenthal; B N Ames
Journal:  Environ Health Perspect       Date:  1987-10       Impact factor: 9.031

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  49 in total

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Review 9.  Chemical and molecular mechanisms of antioxidants: experimental approaches and model systems.

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Review 10.  Assessment of the mode of action underlying development of rodent small intestinal tumors following oral exposure to hexavalent chromium and relevance to humans.

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