Compendium of chemical carcinogens by target organ: results of chronic bioassays in rats, mice, hamsters, dogs, and monkeys
- PMID: 11794380
- DOI: 10.1080/019262301753385979
Compendium of chemical carcinogens by target organ: results of chronic bioassays in rats, mice, hamsters, dogs, and monkeys
Abstract
A compendium of carcinogenesis bioassay results organized by target organ is presented for 738 chemicals that are carcinogenic in chronic-exposure, long-term bioassays in at least 1 species. This compendium is based primarily on experiments in rats or mice; results in hamsters, monkeys, and dogs are also reported. The compendium can be used to identify chemicals that induce tumors at particular sites and to determine whether target sites are the same for chemicals positive in more than 1 species. The source of information is the Carcinogenic Potency Database (CPDB). which includes results of 6073 experiments on 1458 chemicals (positive or negative for carcinogenicity) that have been reported in Technical Reports of the National Cancer Institute/National Toxicology Program or in papers in the general published literature. The published CPDB includes detailed analyses of each test and citations. The CPDB is publicly available in several formats (http://potency.berkeley.edu). Chemical carcinogens are reported for 35 different target organs in rats or mice. Target organs in humans are also summarized for 82 agents that have been evaluated as human carcinogens at a particular target site by the International Agency for Research on Cancer (IARC). Comparisons are provided of target organs for mutagens versus nonmutagens and rats versus mice.
Similar articles
-
Target organs in chronic bioassays of 533 chemical carcinogens.Environ Health Perspect. 1991 Jun;93:233-46. doi: 10.1289/ehp.9193233. Environ Health Perspect. 1991. PMID: 1773795 Free PMC article. Review.
-
Supplement to the Carcinogenic Potency Database (CPDB): results of animal bioassays published in the general literature in 1993 to 1994 and by the National Toxicology Program in 1995 to 1996.Environ Health Perspect. 1999 Aug;107 Suppl 4(Suppl 4):527-600. doi: 10.1289/ehp.99107s4527. Environ Health Perspect. 1999. PMID: 10421768 Free PMC article.
-
Supplement to the Carcinogenic Potency Database (CPDB): results of animal bioassays published in the general literature through 1997 and by the National Toxicology Program in 1997-1998.Toxicol Sci. 2005 Jun;85(2):747-808. doi: 10.1093/toxsci/kfi161. Epub 2005 Mar 30. Toxicol Sci. 2005. PMID: 15800034
-
Sixth plot of the carcinogenic potency database: results of animal bioassays published in the General Literature 1989 to 1990 and by the National Toxicology Program 1990 to 1993.Environ Health Perspect. 1995 Nov;103 Suppl 8(Suppl 8):3-122. doi: 10.1289/ehp.95103s83. Environ Health Perspect. 1995. PMID: 8741772 Free PMC article. Review.
-
The Carcinogenic Potency Database: analyses of 4000 chronic animal cancer experiments published in the general literature and by the U.S. National Cancer Institute/National Toxicology Program.Environ Health Perspect. 1991 Dec;96:11-5. doi: 10.1289/ehp.919611. Environ Health Perspect. 1991. PMID: 1820251 Free PMC article.
Cited by
-
The EDA-deficient mouse has Zymbal's gland hypoplasia and acute otitis externa.Dis Model Mech. 2022 Mar 1;15(3):dmm049034. doi: 10.1242/dmm.049034. Epub 2022 Mar 30. Dis Model Mech. 2022. PMID: 35107126 Free PMC article.
-
Using liver models generated from human-induced pluripotent stem cells (iPSCs) for evaluating chemical-induced modifications and disease across liver developmental stages.Toxicol In Vitro. 2022 Sep;83:105412. doi: 10.1016/j.tiv.2022.105412. Epub 2022 Jun 7. Toxicol In Vitro. 2022. PMID: 35688329 Free PMC article. Review.
-
A novel support vector machine-based 1-day, single-dose prediction model of genotoxic hepatocarcinogenicity in rats.Arch Toxicol. 2024 Aug;98(8):2711-2730. doi: 10.1007/s00204-024-03755-w. Epub 2024 May 18. Arch Toxicol. 2024. PMID: 38762666
-
Preclinical evaluation of efficacy and safety of an improved lentiviral vector for the treatment of β-thalassemia and sickle cell disease.Curr Gene Ther. 2015;15(1):64-81. doi: 10.2174/1566523214666141127095336. Curr Gene Ther. 2015. PMID: 25429463 Free PMC article.
-
Application of humanized mice to toxicology studies: Evaluation of the human relevance of the mode of action for rodent liver tumor formation by activators of the constitutive androstane receptor (CAR).J Toxicol Pathol. 2021 Oct;34(4):283-297. doi: 10.1293/tox.2021-0027. Epub 2021 Jun 27. J Toxicol Pathol. 2021. PMID: 34629731 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources