Literature DB >> 1486853

Nongenotoxic carcinogens: an extension of the perspective provided by Perera.

J Ashby1, I F Purchase.   

Abstract

Perera recently discussed the very real problems that accompany any attempt to classify rodent carcinogens into two groups--genotoxic or nongenotoxic. Not the least of these problems is that no agreed definition of these two terms exist. Nonetheless, the current carcinogen databases, for example, that of the U.S. National Toxicology Program (NTP), clearly comprise two broad groups of carcinogens--DNA reactive, mutagenic and multiply carcinogenic chemicals, and others. The others appear to be nonreactive to DNA, are inactive in the primary mutagenicity assays, and usually elicit highly selective carcinogenic responses in animals. These two classes of carcinogen are illustrated by examples taken from the NTP database and are discussed within the possible context of the latter group not being active in humans or, if they are, only when a threshold dose has been exceeded, chronically.

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Year:  1992        PMID: 1486853      PMCID: PMC1519611          DOI: 10.1289/ehp.9298223

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


  10 in total

1.  Activation of a member of the steroid hormone receptor superfamily by peroxisome proliferators.

Authors:  I Issemann; S Green
Journal:  Nature       Date:  1990-10-18       Impact factor: 49.962

2.  More pieces in the dioxin puzzle.

Authors:  L Roberts
Journal:  Science       Date:  1991-10-18       Impact factor: 47.728

3.  Detection of human carcinogens.

Authors:  J Ashby; R S Morrod
Journal:  Nature       Date:  1991-07-18       Impact factor: 49.962

4.  In reply: carcinogenic risk estimation.

Authors:  B N Ames; L S Gold
Journal:  Science       Date:  1988-05-20       Impact factor: 47.728

Review 5.  Too many rodent carcinogens: mitogenesis increases mutagenesis.

Authors:  B N Ames; L S Gold
Journal:  Science       Date:  1990-08-31       Impact factor: 47.728

Review 6.  Preneoplastic lesions in rodent kidney induced spontaneously or by non-genotoxic agents: predictive nature and comparison to lesions induced by genotoxic carcinogens.

Authors:  D R Dietrich; J A Swenberg
Journal:  Mutat Res       Date:  1991-06       Impact factor: 2.433

7.  Definitive relationships among chemical structure, carcinogenicity and mutagenicity for 301 chemicals tested by the U.S. NTP.

Authors:  J Ashby; R W Tennant
Journal:  Mutat Res       Date:  1991-05       Impact factor: 2.433

8.  Targets for dioxin: genes for plasminogen activator inhibitor-2 and interleukin-1 beta.

Authors:  T R Sutter; K Guzman; K M Dold; W F Greenlee
Journal:  Science       Date:  1991-10-18       Impact factor: 47.728

Review 9.  Perspectives on the risk assessment for nongenotoxic carcinogens and tumor promoters.

Authors:  F P Perera
Journal:  Environ Health Perspect       Date:  1991-08       Impact factor: 9.031

Review 10.  Predicting the carcinogenicity of chemicals in humans from rodent bioassay data.

Authors:  G Goodman; R Wilson
Journal:  Environ Health Perspect       Date:  1991-08       Impact factor: 9.031

  10 in total
  1 in total

1.  Promotion by sodium L-ascorbate in rat two-stage urinary bladder carcinogenesis is dependent on the interval of administration.

Authors:  T X Chen; H Wanibuchi; T Murai; M Kitano; S Yamamoto; S Fukushima
Journal:  Jpn J Cancer Res       Date:  1999-01
  1 in total

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