Evidence of the mutagenicity of ethylene dichloride and structurally related compounds

Fabricant, JD; Chalmers JH Jr

HERO ID

62604

Reference Type

Book/Book Chapter

Year

1980

Language

English

HERO ID 62604
Year 1980
Title Evidence of the mutagenicity of ethylene dichloride and structurally related compounds
Book Title Banbury Report 5: Ethylene Dichloride: A Potential Health Risk?
Authors Fabricant, JD; Chalmers JH Jr
Editor B Ames; P Infante; R Reitz
Publisher Text Cold Spring Harbor Laboratory
City Cold Spring Harbor, NY
Volume 5
Page Numbers 309-329
Abstract A number of short-term methods have been developed in recent years to test chemical compounds and other agents for metagenic activity. These tests involve a number of species, both mammalian and nonmammalian, and are conducted both in vivo and in vitro. A correlation has been shown between the mutagenicity and the carcinogenicity of a compund. It has been estimated that approximately 80% (B.N. Ames, pers. comm.; M.S. Legator, pers. comm.) of all mutagenic compounds are also carcinogenic, although not all carcinogens are mutagens. Therefore, the value of tests to determine the mutagenicity of a compound is important in that these tests may, at least in some cases, give some indication of the carcinogenicity of that chemical as well. The mutagenicity tests alone, however, cannot difinitively identify a carcinogen. However, some of these test can be used for monitoring at-risk population groups and to aid in the evaluation of acceptable exposure standards. Mutational events may occur either at the gene level, where they result in mutant alleles, or at the chromosome level, where they cause chromosomal aberrations (usually the deletions or addition of some part of the chromosome arm). These may occur either during meiosis (in germ cells resulting in possible genetic transmission of that mutation) or during mitosis (occurring in somatic cells and not hereditary). Chromosomal aberrations may be either numerical or structural. Numerical abberations affect the whole chromosome set by the addition or deletion of one or more chromosomes from the cell. Structural anomalies, however, are generally deletions, breaks, gaps, or translocations in choromosomes and do not affect the chromosome number. Although many of these mutational events may result in cellular death, many may be repaired. In addition to the genetic end points of gene mutation or chromosomal aberration primary DNA damage may result from chemical mutagenesis. There are a number of tests that evaluate damage-induced genetic recombination. These include mitotic crossing over, gene coversion, sister chromatid exchange, and unscheduled DNA synthesis, as well as others.
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Comments In: Ames, B.; Infante, P.; Reitz, R., eds. Ethylene dichloride: a potential health risk? Cold Spring Harbor, NY: Cold Spring Harbor Laboratory; pp. 309-329. (Banbury report 5).
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Language Text English
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