Abstract
Human diploid fibroblasts in culture can be very useful for examining the cytotoxic and mutagenic effects of environmental agents (Albertini and DeMars, 1973; Buchwald, 1977; Cox and Masson 1976; Glover et al., 1979; Jacobs and DeMars, 1978; Maher and McCormick, 1976, 1980; Maher and Wessel, 1975; Maher et al., 1975, 1976a,b,c, 1977, 1979; Mankovitz et al., 1974). Studies with these human cells provide a bridge between studies conducted with animal cells in culture and whole animals, on the one hand, and epidemiological studies of the accidental exposure of humans to various agents on the other. In addition, the use of human cells makes it possible to carry out comparative studies designed to elucidate the role of DNA repair in somatic cell mutagenesis (and carcinogenesis) because of the availability of repair-deficient strains derived from individuals with various inherited DNA-repair-deficiency diseases (Fujiwara et al., 1977; German, 1972; Lehmann et al., 1975; Robbins et al., 1974; Taylor et al, 1975).
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Abbreviations
- NF:
-
(normal fibroblasts) i.e., diploid fibroblasts derived from normal individuals
- XP:
-
xeroderma pigmentosum
- AG, 8:
-
azaguanine
- TG, 6:
-
thioguanine
- HX:
-
hypoxanthine
- HPRT:
-
hypoxanthine(guanine) phosphoribosyltransferase
- PBS:
-
phosphate buffered saline, pH 7.2.
References
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McCormick, J.J., Maher, V.M. (1981). Mutagenesis Studies in Diploid Human Cells with Different DNA-Repair Capacities. In: Stich, H.F., San, R.H.C. (eds) Short-Term Tests for Chemical Carcinogens. Topics in Environmental Physiology and Medicine. Springer, New York, NY. https://doi.org/10.1007/978-1-4612-5847-6_24
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DOI: https://doi.org/10.1007/978-1-4612-5847-6_24
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