Skip Navigation

Publication Detail

Title: Genotoxic markers among butadiene polymer workers in China.

Authors: Hayes, R B; Zhang, L; Yin, S; Swenberg, J A; Xi, L; Wiencke, J; Bechtold, W E; Yao, M; Rothman, N; Haas, R; O'Neill, J P; Zhang, D; Wiemels, J; Dosemeci, M; Li, G; Smith, M T

Published In Carcinogenesis, (2000 Jan)

Abstract: While 1,3-butadiene is carcinogenic in rodents, cancer causation in humans is less certain. We examined a spectrum of genotoxic outcomes in 41 butadiene polymer production workers and 38 non-exposed controls, in China, to explore the role of butadiene in human carcinogenesis. Because in vitro studies suggest that genetic polymorphisms in glutathione S-transferase enzymes influence genotoxic effects of butadiene, we also related genotoxicity to genetic polymorphisms in GSTT1 and GSTM1. Among butadiene-exposed workers, median air exposure was 2 p.p.m. (6 h time-weighted average), due largely to intermittent high level exposures. Compared with unexposed subjects, butadiene-exposed workers had greater levels of hemoglobin N-(2,3,4-trihydroxybutyl)valine (THBVal) adducts (P < 0.0001) and adduct levels tended to correlate, among butadiene-exposed workers, with air measures (P = 0.03). Butadiene-exposed workers did not differ, however, from unexposed workers with respect to frequency of uninduced or diepoxybutane-induced sister chromatid exchanges, aneuploidy as measured by fluorescence in situ hybridization of chromosomes 1, 7, 8 and 12, glycophorin A variants or lymphocyte hprt somatic mutation. Also among the exposed, greater THBVal levels were not associated with increases in uninduced sister chromatid exchanges, aneuploidy, glycophorin A or hprt mutations. Butadiene-exposed workers had greater lymphocyte (P = 0.002) and platelet counts (P = 0.07) and lymphocytes as a percentage of white blood cells were moderately correlated with greater THBVal levels (Spearman's phi = 0.32, P = 0.07). Among butadiene-exposed workers, neither GSTM1 nor GSTT1 genotype status predicted urinary mercapturic acid butanediol formation, THBVal adducts, uninduced sister chromatid exchanges, aneuploidy or mutations in the glycophorin A or hprt genes. Overall, the study demonstrated exposure to butadiene in these workers, by a variety of short-term and long-term measures, but did not show specific genotoxic effects, at the chromosomal or gene levels, related to that exposure.

PubMed ID: 10607734 Exiting the NIEHS site

MeSH Terms: Adult; Biomarkers; Butadienes/toxicity*; Chromosome Aberrations; Female; Glutathione Transferase/genetics; Hemoglobins/metabolism; Humans; Male; Mutagens/toxicity*; Occupational Exposure*; Sister Chromatid Exchange; Valine/analogs & derivatives; Valine/metabolism

Back
to Top