Literature DB >> 2197145

Refinement of long-term toxicity and carcinogenesis studies.

G N Rao1, J Huff.   

Abstract

The chance that alternatives will completely replace animals for toxicology research in the foreseeable future is nil. Continual refinement of animal toxicity and carcinogenesis studies, however, can be an effective means of reducing the numbers of animals used and conserving time and resources without compromising scientific quality. We must continue to strive to find species and strains that can metabolize chemicals similar to humans, are small enough to be housed in large numbers, and have low prevalence of spontaneous lesions with sufficient life span to express the toxic and carcinogenic potential of chemicals. Adequate care of animals with control of variables such as light, temperature, diet, bedding, diseases, and genetic characters of laboratory animals will decrease the variability. Humane considerations and euthanasia of animals with large masses and other conditions interfering with eating and drinking, major injuries and ulcers related to husbandry and treatment, and diseases indicating pain and suffering will help not only to alleviate further pain and distress but also to facilitate collection of tissues without secondary complications for detection of chemical treatment-related lesions. Limiting the duration of studies to decrease the variability due to age-associated changes will also refine long-term studies. Other considerations for refinement of carcinogenesis studies include selection of the most sensitive sex of one or more species for evaluation of selected chemicals in a class where toxic and carcinogenic potential of other representative chemicals are known. Genetically engineered animal models with known oncogenes may reduce the duration and increase the sensitivity of carcinogenesis studies with a reduction in the use of animals.

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Year:  1990        PMID: 2197145      PMCID: PMC7126419          DOI: 10.1016/0272-0590(90)90160-l

Source DB:  PubMed          Journal:  Fundam Appl Toxicol        ISSN: 0272-0590


  17 in total

1.  Fluorescent lighting enhances chemically induced papilloma formation and increases susceptibility to tumor challenge in mice.

Authors:  A Wiskemann; E Sturm; N W Klehr
Journal:  J Cancer Res Clin Oncol       Date:  1986       Impact factor: 4.553

2.  Safety evaluation of fish protein concentrate over five generations of rats.

Authors:  P M Newberne; O Glaser; L Friedman; B Stillings
Journal:  Toxicol Appl Pharmacol       Date:  1973-01       Impact factor: 4.219

3.  Prediction of chemical carcinogenicity in rodents from in vitro genetic toxicity assays.

Authors:  R W Tennant; B H Margolin; M D Shelby; E Zeiger; J K Haseman; J Spalding; W Caspary; M Resnick; S Stasiewicz; B Anderson
Journal:  Science       Date:  1987-05-22       Impact factor: 47.728

Review 4.  Mouse strains for chemical carcinogenicity studies: overview of a workshop.

Authors:  G N Rao; L S Birnbaum; J J Collins; R W Tennant; L C Skow
Journal:  Fundam Appl Toxicol       Date:  1988-04

5.  Lighting in the animal environment.

Authors:  R W Bellhorn
Journal:  Lab Anim Sci       Date:  1980-04

6.  Influence of viral infections on body weight, survival, and tumor prevalence in Fischer 344/NCr rats on two-year studies.

Authors:  G N Rao; J K Haseman; J Edmondson
Journal:  Lab Anim Sci       Date:  1989-09

7.  Neoplasms observed in untreated and corn oil gavage control groups of F344/N rats and (C57BL/6N X C3H/HeN)F1 (B6C3F1) mice.

Authors:  J K Haseman; J E Huff; G N Rao; J E Arnold; G A Boorman; E E McConnell
Journal:  J Natl Cancer Inst       Date:  1985-11       Impact factor: 13.506

8.  NTP Toxicology and Carcinogenesis Studies of Nalidixic Acid (CAS No. 389-08-2) in F344/N Rats and B6C3F1 Mice (Feed Studies).

Authors: 
Journal:  Natl Toxicol Program Tech Rep Ser       Date:  1989-10

9.  Influence of viral infections on body weight, survival, and tumor prevalence of B6C3F1 (C57BL/6N x C3H/HeN) mice in carcinogenicity studies.

Authors:  G N Rao; W W Piegorsch; D D Crawford; J Edmondson; J K Haseman
Journal:  Fundam Appl Toxicol       Date:  1989-07

10.  Sources of variability in rodent carcinogenicity studies.

Authors:  J K Haseman; J E Huff; G N Rao; S L Eustis
Journal:  Fundam Appl Toxicol       Date:  1989-05
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  2 in total

Review 1.  Chemicals associated with site-specific neoplasia in 1394 long-term carcinogenesis experiments in laboratory rodents.

Authors:  J Huff; J Cirvello; J Haseman; J Bucher
Journal:  Environ Health Perspect       Date:  1991-06       Impact factor: 9.031

2.  Long-term chemical carcinogenesis experiments for identifying potential human cancer hazards: collective database of the National Cancer Institute and National Toxicology Program (1976-1991).

Authors:  J Huff; J Haseman
Journal:  Environ Health Perspect       Date:  1991-12       Impact factor: 9.031

  2 in total

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