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HPRT Mutations in Lymphocytes from 1,3-Butadiene-Exposed Workers in China

BACKGROUND: 1,3-Butadiene (BD) is an important industrial chemical and an environmental and occupational pollutant. The carcinogenicity of BD in rodents has been proved, but its carcinogenic and mutagenic molecular mechanism(s) are not fully elucidated in humans. OBJECTIVES: In the present study, we...

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Autores principales: Liu, Shengxue, Ao, Lin, Du, Bing, Zhou, Yanhong, Yuan, Jian, Bai, Yang, Zhou, Ziyuan, Cao, Jia
Formato: Texto
Lenguaje:English
Publicado: National Institute of Environmental Health Sciences 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2235214/
https://www.ncbi.nlm.nih.gov/pubmed/18288319
http://dx.doi.org/10.1289/ehp.10353
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author Liu, Shengxue
Ao, Lin
Du, Bing
Zhou, Yanhong
Yuan, Jian
Bai, Yang
Zhou, Ziyuan
Cao, Jia
author_facet Liu, Shengxue
Ao, Lin
Du, Bing
Zhou, Yanhong
Yuan, Jian
Bai, Yang
Zhou, Ziyuan
Cao, Jia
author_sort Liu, Shengxue
collection PubMed
description BACKGROUND: 1,3-Butadiene (BD) is an important industrial chemical and an environmental and occupational pollutant. The carcinogenicity of BD in rodents has been proved, but its carcinogenic and mutagenic molecular mechanism(s) are not fully elucidated in humans. OBJECTIVES: In the present study, we compared the mutation frequencies and exon deletions of BD-exposed workers with that of control subjects in China to identify the characteristic mutations associated with BD exposure in the human HPRT (hypoxanthine–guanine–phosphoribosyltransferase) gene. METHODS: Seventy-four workers exposed to BD via inhalation and 157 matched controls were evaluated in Nanjing, China. Molecular analysis of HPRT mutant T lymphocytes from BD-exposed workers and nonexposed control subjects was conducted to identify changes in the structure of the HPRT gene. A total of 783 HPRT mutants were analyzed by multiplex polymerase chain reaction, in which 368 HPRT mutants were isolated from BD-exposed workers and 415 mutants from control subjects. RESULTS: The BD-exposed workers showed a higher mutation frequency (18.2 ± 9.4 × 10(−6)) than the control subjects (12.7 ± 7.3 × 10(−6)), but the difference was not significant (p > 0.05). The frequency of exon deletions in BD-exposed workers (27.4%) was significantly higher than that in control subjects (12.5%) (p < 0.05), which mainly included multiplex exon deletions (2–8 exons). CONCLUSIONS: The results of the present study suggest that BD should increase the frequency of large deletions of HPRT gene in human lymphocytes This change confirms and supports the previous findings in BD-exposed workers.
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spelling pubmed-22352142008-02-20 HPRT Mutations in Lymphocytes from 1,3-Butadiene-Exposed Workers in China Liu, Shengxue Ao, Lin Du, Bing Zhou, Yanhong Yuan, Jian Bai, Yang Zhou, Ziyuan Cao, Jia Environ Health Perspect Research BACKGROUND: 1,3-Butadiene (BD) is an important industrial chemical and an environmental and occupational pollutant. The carcinogenicity of BD in rodents has been proved, but its carcinogenic and mutagenic molecular mechanism(s) are not fully elucidated in humans. OBJECTIVES: In the present study, we compared the mutation frequencies and exon deletions of BD-exposed workers with that of control subjects in China to identify the characteristic mutations associated with BD exposure in the human HPRT (hypoxanthine–guanine–phosphoribosyltransferase) gene. METHODS: Seventy-four workers exposed to BD via inhalation and 157 matched controls were evaluated in Nanjing, China. Molecular analysis of HPRT mutant T lymphocytes from BD-exposed workers and nonexposed control subjects was conducted to identify changes in the structure of the HPRT gene. A total of 783 HPRT mutants were analyzed by multiplex polymerase chain reaction, in which 368 HPRT mutants were isolated from BD-exposed workers and 415 mutants from control subjects. RESULTS: The BD-exposed workers showed a higher mutation frequency (18.2 ± 9.4 × 10(−6)) than the control subjects (12.7 ± 7.3 × 10(−6)), but the difference was not significant (p > 0.05). The frequency of exon deletions in BD-exposed workers (27.4%) was significantly higher than that in control subjects (12.5%) (p < 0.05), which mainly included multiplex exon deletions (2–8 exons). CONCLUSIONS: The results of the present study suggest that BD should increase the frequency of large deletions of HPRT gene in human lymphocytes This change confirms and supports the previous findings in BD-exposed workers. National Institute of Environmental Health Sciences 2008-02 2007-11-12 /pmc/articles/PMC2235214/ /pubmed/18288319 http://dx.doi.org/10.1289/ehp.10353 Text en http://creativecommons.org/publicdomain/mark/1.0/ Publication of EHP lies in the public domain and is therefore without copyright. All text from EHP may be reprinted freely. Use of materials published in EHP should be acknowledged (for example, ?Reproduced with permission from Environmental Health Perspectives?); pertinent reference information should be provided for the article from which the material was reproduced. Articles from EHP, especially the News section, may contain photographs or illustrations copyrighted by other commercial organizations or individuals that may not be used without obtaining prior approval from the holder of the copyright.
spellingShingle Research
Liu, Shengxue
Ao, Lin
Du, Bing
Zhou, Yanhong
Yuan, Jian
Bai, Yang
Zhou, Ziyuan
Cao, Jia
HPRT Mutations in Lymphocytes from 1,3-Butadiene-Exposed Workers in China
title HPRT Mutations in Lymphocytes from 1,3-Butadiene-Exposed Workers in China
title_full HPRT Mutations in Lymphocytes from 1,3-Butadiene-Exposed Workers in China
title_fullStr HPRT Mutations in Lymphocytes from 1,3-Butadiene-Exposed Workers in China
title_full_unstemmed HPRT Mutations in Lymphocytes from 1,3-Butadiene-Exposed Workers in China
title_short HPRT Mutations in Lymphocytes from 1,3-Butadiene-Exposed Workers in China
title_sort hprt mutations in lymphocytes from 1,3-butadiene-exposed workers in china
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2235214/
https://www.ncbi.nlm.nih.gov/pubmed/18288319
http://dx.doi.org/10.1289/ehp.10353
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