Prevalence of genotoxic chemicals among animal and human carcinogens evaluated in the IARC Monograph series.
- 1 June 1989
- journal article
- research article
- Published by Springer Nature in Cell Biology and Toxicology
- Vol. 5 (2) , 115-127
- https://doi.org/10.1007/bf00122647
Abstract
To determine whether genotoxic and non-genotoxic carcinogens contribute similarly to the cancer burden in humans, an analysis was performed on agents that were evaluated in Supplements 6 and 7 to the IARC Monographs for their carcinogenic effects in humans and animals and for the activity in short-term genotoxicity tests. The prevalence of genotoxic carcinogens on four groups of agents, consisting of established human carcinogens (group 1, n = 30), probable human carcinogens (group 2A, n = 37), possible human carcinogens (group 2B, n = 113) and on agents with limited evidence of carcinogenicity in animals (a subset of group 3, n = 149) was determined. A high prevalence in the order of 80 to 90% of genotoxic carcinogens was found in each of the groups 1, 2A and 2B, which were also shown to be multi-species/multi-tissues carcinogens. The distribution of carcinogenic potency in rodents did not reveal any specific characteristic of the human carcinogens in group 1 that would differentiate them from agents in groups 2A, 2B and 3. The results of this analysis indicate that (a) an agent with unknown carcinogenic potential showing sufficient evidence of activity in in vitro / in vivo genotoxicity assays (involving as endpoints DNA damage and chromosomal/mutational damage) may represent a hazard to humans; and (b) an agent showing lack of activity in this spectrum of genotoxicity assays should undergo evaluation for carcinogenicity by rodent bioassay, in view of the present lack of validated short-term tests for non-genotoxic carcinogens. Overall, this analysis implies that genotoxic carcinogens add more to the cancer burden in man than non-genotoxic carcinogens. Thus, identification of such genotoxic carcinogens and subsequent lowering of exposure will remain the main goal for primary cancer prevention in man.Keywords
This publication has 12 references indexed in Scilit:
- Quantifying the carcinogenicity of antineoplastic drugsEuropean Journal of Cancer and Clinical Oncology, 1988
- Chemical structure, Salmonella mutagenicity and extent of carcinogenicity as indicators of genotoxic carcinogenesis among 222 chemicals tested in rodents by the U.S. NCI/NTPMutation Research/Genetic Toxicology, 1988
- The genetic toxicity of human carcinogens and its implicationsMutation Research/Genetic Toxicology, 1988
- Commentary on the status of short‐term tests for chemical carcinogensEnvironmental and Molecular Mutagenesis, 1988
- Utility of short‐term tests for genetic toxicity in the aftermath of the NTP's analysis of 73 chemicalsEnvironmental and Molecular Mutagenesis, 1988
- Prediction of Chemical Carcinogenicity in Rodents from in Vitro Genetic Toxicity AssaysScience, 1987
- Performance of short-term tests for detection of human carcinogensMutagenesis, 1987
- Overall evaluations of carcinogenicity: an updating of IARC Monographs volumes 1 to 42.1987
- The Salmonella typhimurium/mammalian microsomal assayMutation Research/Reviews in Genetic Toxicology, 1986
- A carcinogenic potency database of the standardized results of animal bioassaysEnvironmental Health Perspectives, 1984