The carcinogenesis bioassay in perspective: application in identifying human cancer hazards.

The selection process for chemicals tested in the rodent carcinogenicity bioassay has been biased toward chemicals suspected of potential carcinogenicity. Results from carcinogenicity bioassays of 400 chemicals tested by the National Cancer Institute/National Toxicology Program (NCI/NTP) were analyzed to determine the dependence of positive results on chemical selection criteria: those suspected of being carcinogenic and those selected based on large volumes produced and widespread exposures. Of these chemicals, 210 (52%) induced carcinogenicity in at least one organ of one sex of one species of the four sex/species groups typically used by NCI/NTP. Only 92 of the 400 chemicals (23%) were positive in two species and thus by international criteria are considered likely to pose a carcinogenic hazard to humans. A total of 267 chemicals (67%) were selected as suspect carcinogens, and 187 (68%) of these were carcinogenic. Suspect chemicals account for 86% of chemicals with at least one positive result and account for 90% of chemicals considered positive in two species. The International Agency for Research on Cancer (IARC) lists only 5 of the 400 chemicals as carcinogenic to humans (group 1) and 10 as probably carcinogenic to humans (group 2A). The majority (80%) of the 133 chemicals selected only on production/exposure considerations were not carcinogenic in animals, even when tested at the maximum tolerated (or minimally toxic) dose. Only 9 (6.8%) were positive in two species, and none is listed in IARC groups 1 or 2A. Thus, on the basis of our analyses we predict that less than 5-10% of the 75,000 chemicals in commercial use might be reasonably anticipated to be carcinogenic to humans. Imagesp680-a

[1]  A. Aitio,et al.  Human Carcinogens So Far Identified , 1989, Japanese journal of cancer research : Gann.

[2]  R W Tennant,et al.  Predicting chemical carcinogenesis in rodents. , 1993, Environmental health perspectives.

[3]  J. Huff,et al.  Issues and controversies surrounding qualitative strategies for identifying and forecasting cancer causing agents in the human environment. , 1993, Pharmacology & toxicology.

[4]  J. Huff,et al.  Absence of morphologic correlation between chemical toxicity and chemical carcinogenesis. , 1993, Environmental health perspectives.

[5]  L. Tomatis The predictive value of rodent carcinogenicity tests in the evaluation of human risks. , 1979, Annual review of pharmacology and toxicology.

[6]  J. Huff Design strategies, results and evaluations of long-term chemical carcinogenesis studies. , 1992, Scandinavian journal of work, environment & health.

[7]  J. Huff,et al.  Cellular and molecular mechanisms of hormonal carcinogenesis. Environmental influences. , 1996, Progress in clinical and biological research.

[8]  G Zbinden,et al.  Predictive value of animal studies in toxicology. , 1991, Regulatory toxicology and pharmacology : RTP.

[9]  D G Hoel,et al.  Predictive strategies for selecting 379 NCI/NTP chemicals evaluated for carcinogenic potential: scientific and public health impact. , 1993, Fundamental and applied toxicology : official journal of the Society of Toxicology.

[10]  J. Huff,et al.  Chemicals and cancer in humans: first evidence in experimental animals. , 1993, Environmental health perspectives.

[11]  J M Ward,et al.  Factors in the evaluation of 200 National Cancer Institute carcinogen bioassays. , 1981, Journal of toxicology and environmental health.

[12]  J. Kaldor,et al.  Response of experimental animals to human carcinogens: an analysis based upon the IARC Monographs programme. , 1986, Carcinogenesis.

[13]  M. Pike,et al.  Increased cell division as a cause of human cancer. , 1990, Cancer research.

[14]  J. Huff,et al.  Liver Carcinogenesis is Not a Predicted Outcome of Chemically Induced Hepatocyte Proliferation , 1993, Toxicology and industrial health.

[15]  Mechanisms of action of known human carcinogens. , 1992, IARC scientific publications.

[16]  R. Tennant,et al.  Prediction of the outcome of rodent carcinogenicity bioassays currently being conducted on 44 chemicals by the National Toxicology Program. , 1990, Mutagenesis.

[17]  L. Kolonel,et al.  Rationale and strategies for chemoprevention of cancer in humans. , 1987, Cancer research.

[18]  E. Weisburger History of the Bioassay Program of the National Cancer Institute. , 1983, Progress in experimental tumor research.

[19]  H. Vainio Mechanisms of Carcinogenesis in Risk Identification , 1992 .

[20]  J. Huff,et al.  Cell proliferation and chemical carcinogenesis: symposium overview. , 1993, Environmental health perspectives.

[21]  J. Huff,et al.  Perspective and overview of the concepts and value of hazard identification as the initial phase of risk assessment for cancer and human health. , 1992, Scandinavian journal of work, environment & health.

[22]  Huff Je Chemical toxicity and chemical carcinogenesis. Is there a causal connection? A comparative morphological evaluation of 1500 experiments. , 1992 .

[23]  J. Huff,et al.  Carcinogenesis Studies: Results of 398 Experiments on 104 Chemicals from the U. S. National Toxicology Program , 1988, Annals of the New York Academy of Sciences.

[24]  J. Selkirk,et al.  An overview of prechronic and chronic toxicity/carcinogenicity experimental study designs and criteria used by the National Toxicology Program. , 1990, Environmental health perspectives.

[25]  J. Barrett,et al.  Genetic and cellular basis of multistep carcinogenesis. , 1990, Pharmacology & therapeutics.

[26]  J. Huff,et al.  Scientific concepts, value, and significance of chemical carcinogenesis studies. , 1991, Annual review of pharmacology and toxicology.

[27]  E. Somers International Agency for Research on Cancer. , 1985, CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne.

[28]  I. Weinstein,et al.  Mitogenesis is only one factor in carcinogenesis. , 1991, Science.

[29]  R. Tennant,et al.  Stratification of rodent carcinogenicity bioassay results to reflect relative human hazard. , 1993, Mutation research.

[30]  J. Barrett,et al.  Mechanisms of multistep carcinogenesis and carcinogen risk assessment. , 1993, Environmental health perspectives.

[31]  J. Huff,et al.  Mechanisms, chemical carcinogenesis, and risk assessment: cell proliferation and cancer. , 1995, American journal of industrial medicine.

[32]  W. Lijinsky Species differences in carcinogenesis. , 1993, In vivo.

[33]  N. Page,et al.  Guidelines for carcinogen bioassay in small rodents. , 1976, National Cancer Institute carcinogenesis technical report series.

[34]  Dennis Bahler,et al.  The Induction of Rules for Predicting Chemical Carcinogenesis in Rodents , 1993, ISMB.

[35]  B. Ames,et al.  Too many rodent carcinogens: mitogenesis increases mutagenesis. , 1990, Science.

[36]  J. Huff Chemical toxicity and chemical carcinogenesis. Is there a causal connection? A comparative morphological evaluation of 1500 experiments. , 1992, IARC scientific publications.