Literature DB >> 9370513

The significance of mouse liver tumor formation for carcinogenic risk assessment: results and conclusions from a survey of ten years of testing by the agrochemical industry.

N G Carmichael1, H Enzmann, I Pate, F Waechter.   

Abstract

A survey was performed on the results of 138 carcinogenicity studies conducted in various mouse strains by the agrochemical industry over the period 1983-1993. Data for liver tumor incidence, liver weight, and histopathology were collected along with data on genotoxicity. Studies were judged positive or negative for liver tumor formation on the basis of apparent dose response, malignancy, and difference from historical control values using a weight of evidence approach. Thirty-seven studies were judged to be positive for liver tumorigenicity in one or both sexes. There was no evidence showing an influence of the mouse strain and the duration of the study on the proportion of positive studies. Although 8 of the chemicals tested in the 138 studies were positive in the Ames test, only one of these was judged positive for carcinogenicity. Only 6 of the 37 positive chemicals had any other reported positive genotoxicity findings. A clear relationship between hepatomegaly at 1 year after exposure and a positive tumorigenic outcome at 18 months or 2 years after exposure was demonstrated. Whereas the average relative liver weight of top dose animals was 110% of control in negative studies, it was 150% in positive studies. Likewise, very few negative studies demonstrated significant pathological findings after 1 year, whereas the majority of positive studies had significant liver pathology. The implications of these findings for extrapolation to humans are discussed.

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Year:  1997        PMID: 9370513      PMCID: PMC1470341          DOI: 10.1289/ehp.971051196

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


  36 in total

Review 1.  Hepatitis B virus. The major etiology of hepatocellular carcinoma.

Authors:  R P Beasley
Journal:  Cancer       Date:  1988-05-15       Impact factor: 6.860

Review 2.  Liver lesions in B6C3F1 mice: the National Toxicology Program, experience and position.

Authors:  R R Maronpot; J K Haseman; G A Boorman; S E Eustis; G N Rao; J E Huff
Journal:  Arch Toxicol Suppl       Date:  1987

3.  Hepatocellular carcinoma and its risk factors--their annual changes and effects on the age at onset.

Authors:  G Yamaguchi
Journal:  Kurume Med J       Date:  1993

4.  Occupational risks for primary liver cancer in Shanghai, China.

Authors:  W H Chow; J K McLaughlin; W Zheng; W J Blot; Y T Gao
Journal:  Am J Ind Med       Date:  1993-07       Impact factor: 2.214

5.  Drug metabolism in man and its relationship to that in three rodent species: monooxygenase, epoxide hydrolase, and glutathione S-transferase activities in subcellular fractions of lung and liver.

Authors:  J Lorenz; H R Glatt; R Fleischmann; R Ferlinz; F Oesch
Journal:  Biochem Med       Date:  1984-08

6.  Hepatitis B virus, cigarette smoking and alcohol consumption in the development of hepatocellular carcinoma: a case-control study in Fukuoka, Japan.

Authors:  K Tanaka; T Hirohata; S Takeshita; I Hirohata; S Koga; K Sugimachi; T Kanematsu; F Ohryohji; H Ishibashi
Journal:  Int J Cancer       Date:  1992-06-19       Impact factor: 7.396

7.  Alcohol consumption as a risk factor for hepatocellular carcinoma in urban southern African blacks.

Authors:  A E Mohamed; M C Kew; H T Groeneveld
Journal:  Int J Cancer       Date:  1992-06-19       Impact factor: 7.396

8.  Correlations between chemically related site-specific carcinogenic effects in long-term studies in rats and mice.

Authors:  J K Haseman; A M Lockhart
Journal:  Environ Health Perspect       Date:  1993-04-22       Impact factor: 9.031

Review 9.  Target organs in chronic bioassays of 533 chemical carcinogens.

Authors:  L S Gold; T H Slone; N B Manley; L Bernstein
Journal:  Environ Health Perspect       Date:  1991-06       Impact factor: 9.031

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  5 in total

1.  Thiamethoxam induced hepatotoxicity and pro-carcinogenicity in rabbits via motivation of oxidative stress, inflammation, and anti-apoptotic pathway.

Authors:  Osama S El Okle; Omnia I El Euony; Asmaa F Khafaga; Mohamed A Lebda
Journal:  Environ Sci Pollut Res Int       Date:  2017-12-01       Impact factor: 4.223

2.  Biological Basis of Differential Susceptibility to Hepatocarcinogenesis among Mouse Strains.

Authors:  Robert R Maronpot
Journal:  J Toxicol Pathol       Date:  2009-04-06       Impact factor: 1.628

3.  The p53 heterozygous knockout mouse as a model for chemical carcinogenesis in vascular tissue.

Authors:  N G Carmichael; E L Debruyne; D Bigot-Lasserre
Journal:  Environ Health Perspect       Date:  2000-01       Impact factor: 9.031

Review 4.  Prediction of the Carcinogenic Potential of Human Pharmaceuticals Using Repeated Dose Toxicity Data and Their Pharmacological Properties.

Authors:  Jan Willem van der Laan; Wenny H W Buitenhuis; Laura Wagenaar; Ans E M F Soffers; Eugene P van Someren; Cyrille A M Krul; Ruud A Woutersen
Journal:  Front Med (Lausanne)       Date:  2016-10-14

5.  Harmful Algal Bloom Toxicity in Lithobates catesbeiana Tadpoles.

Authors:  Robin C Su; Casey M Meyers; Emily A Warner; Jessica A Garcia; Jeanine M Refsnider; Apurva Lad; Joshua D Breidenbach; Nikolai Modyanov; Deepak Malhotra; Steven T Haller; David J Kennedy
Journal:  Toxins (Basel)       Date:  2020-06-08       Impact factor: 4.546

  5 in total

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