The Use of Human Cells for the Evaluation of Risk from Physical and Chemical Agents pp 767-771 | Cite as
In Vitro Studies on Chemical Carcinogenesis in BALB/c 3T3 Cells
Chapter
Abstract
During the last decade many in vitro systems have been developed as short-term tests for chemical, viral and physical carcinogenesis. A complete battery of such tests should include bacterial and mammalian mutagenesis, chromosome tests, DNA repair and cell transformation. These tests have been developed on the assumption that the oncogenic event is based on a genotoxic mechanism, the endpoint of which is detectable in a qualitative or quantitative way in each system.
Keywords
Transformation Frequency Chemical Carcinogen Chemical Carcinogenesis Mouse Embryo Fibroblast Cell Chromosome Test
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References
- 1.B. N. Ames, J. McCann, and E. Yamasaki, Methods for detecting carcinogens and mutagens with the Salmonella/mammalian-microsome mutagenicity test, Mut. Res., 31: 347 (1975).Google Scholar
- 2.U. Saffiotti, P. J. Donovan, J. M. Rice, and E. Cortesi, Mutual synergism in Salmonella mutagenesis by aflatoxin B1, benzidine, benzo[a]pyrene and safrole, Teratogenesis, Carcinogenesis, and Mutagenesis (in press).Google Scholar
- 3.S. A. Aaronson and G. J. Todaro, Development of 3T3-like lines from BALB/c mouse embryo cultures: transformation susceptibility to SV 40, Science, 162: 1024 (1968).PubMedCrossRefGoogle Scholar
- 4.J. A. Di Paolo, K. Takano, and N. C. Popescu, Quantitation of chemically induced neoplastic transformation of BALB/3T3 cloned cell lines, Cancer Res., 32: 2686 (1970).Google Scholar
- 5.T. Kakunaga and J. Kamohora, Process of neoplastic transformation of cultured mammalian cell by chemical carcinogens, J. Cancer Assoc. Proc. Symp. 29th, p. 42 (1970).Google Scholar
- 6.T. Kakunaga and K. Miyashita, The involvement of DNA lesions and repair system in the cell transformation by chemical carcinogens, Symp. Cell Biol., Vol. 23: 95 (1972).Google Scholar
- 7.T. Kakunaga, A quantitative system for assay of maligant transformation by chemical carcinogens using a clone derived from BALB/3T3, Int. J. Cancer, 12: 463 (1973).PubMedCrossRefGoogle Scholar
- 8.T. Kakunaga and J. D. Crow, Cell variants showing differential susceptibility to ultraviolet light-induced-transformation, Science, 209: 505 (1980).PubMedCrossRefGoogle Scholar
- 9.A. Sivak et al., BALB/c-3T3 cells as target cells for chemically induced neoplastic transformation, Adv. Environ. Toxicol. (in press).Google Scholar
- 10.L. M. Schechtman and R. E. Kouri, Control of benzo(a)pyrene induced mammalian cell cytotoxicity, mutagenesis,and transformation by exogenous enzyme fractions, Progress in Genetic Toxicology: 307 (1977).Google Scholar
- 11.T. V. Zenser, M. B. Mattammal, H. J. Armbrecht, and B. B. David, Benzidine binding to nucleic acids mediated by the per-oxidative activity of prostaglandin endoperoxidase synthetase, Cancer Res., 40: 2839 (1980).PubMedGoogle Scholar
- 12.E. Cortesi, U. Saffiotti, P. J. Donovan, J. M. Rice, and T. Kakunaga, Dose–response studies on neoplastic transformation of BALB/c 3T3 clone A31–1–1 cells by aflatoxin Bi, benzidine, benzo(a)pyrene, 3–methylcholantrene and N–methyl–N’–nitro–Nnitrosoguanidine, Teratogenesis, Carcinogenesis, and Muta–genesis (in press).Google Scholar
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© Springer Science+Business Media New York 1983