An Association of UDP-Glucuronosyltransferase 2B7 C802T (His268Tyr) Polymorphism with Bladder Cancer in Benzidine-Exposed Workers in China
UDP-Glucuronyltransferase 2B7 (UGT2B7) is involved in benzidine metabolism, as demonstrated by in vitro experiments with liver slices. To evaluate the possible association of UGT2B7 gene polymorphism with bladder cancer risk for benzidine-exposed subjects, diagnosed bladder cancer cases (n = 36) who...
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Published in | Toxicological sciences Vol. 85; no. 1; pp. 502 - 506 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
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United States
Oxford University Press
01.05.2005
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Abstract | UDP-Glucuronyltransferase 2B7 (UGT2B7) is involved in benzidine metabolism, as demonstrated by in vitro experiments with liver slices. To evaluate the possible association of UGT2B7 gene polymorphism with bladder cancer risk for benzidine-exposed subjects, diagnosed bladder cancer cases (n = 36) who were members of a cohort of benzidine-exposed workers in the Chinese dyestuff industry were investigated. UGT2B7 polymorphism at locus C802T (His268Tyr) was detected using a PCR-RFLP based procedure. Nondiseased cohort members (156 men, 95 women) were taken as work-related control, and unexposed healthy individuals (113 men, 105 women) were taken as community control. The data showed that the polymorphism at locus UGT2B7 C802T in a general Chinese population significantly differs from that in a Caucasian population (p = 0.00018), displaying a distinctly lower frequency of T/T genotypes (9.2 vs. 25.3%), while no significant difference to a Japanese population could be detected (p = 0.17). A higher prevalence of T/T genotype carriers was found in the cancer cases, compared with unexposed healthy controls (25 vs. 9%, odds ratio [OR] 3.30, 95% confidence interval [95% CI] 1.37–7.98, p = 0.006). A higher presentation of T allele carriers in the patients group was also confirmed (46 vs. 33%, OR 1.73, 95% CI 1.05–2.87, p = 0.03). A higher portion of the T/T genotype was also observed in bladder cancer patients compared with nondiseased members of the same benzidine-exposed cohort, although some of them displayed different degrees of cellular alterations in their exfoliated urothelial cells. This study points for the first time to an association between a homozygous mutant genotype of human UDP-glucuronosyltransferase 2B7 catalyzing the biotransformation of benzidine and an elevated bladder cancer risk for formerly benzidine-exposed workers of the dyestuff industry. |
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AbstractList | UDP-Glucuronyltransferase 2B7 (UGT2B7) is involved in benzidine metabolism, as demonstrated by in vitro experiments with liver slices. To evaluate the possible association of UGT2B7 gene polymorphism with bladder cancer risk for benzidine-exposed subjects, diagnosed bladder cancer cases (n = 36) who were members of a cohort of benzidine-exposed workers in the Chinese dyestuff industry were investigated. UGT2B7 polymorphism at locus C802T (His268Tyr) was detected using a PCR-RFLP based procedure. Nondiseased cohort members (156 men, 95 women) were taken as work-related control, and unexposed healthy individuals (113 men, 105 women) were taken as community control. The data showed that the polymorphism at locus UGT2B7 C802T in a general Chinese population significantly differs from that in a Caucasian population (p = 0.00018), displaying a distinctly lower frequency of T/T genotypes (9.2 vs. 25.3%), while no significant difference to a Japanese population could be detected (p = 0.17). A higher prevalence of T/T genotype carriers was found in the cancer cases, compared with unexposed healthy controls (25 vs. 9%, odds ratio [OR] 3.30, 95% confidence interval [95% CI] 1.37-7.98, p = 0.006). A higher presentation of T allele carriers in the patients group was also confirmed (46 vs. 33%, OR 1.73, 95% CI 1.05-2.87, p = 0.03). A higher portion of the T/T genotype was also observed in bladder cancer patients compared with nondiseased members of the same benzidine-exposed cohort, although some of them displayed different degrees of cellular alterations in their exfoliated urothelial cells. This study points for the first time to an association between a homozygous mutant genotype of human UDP-glucuronosyltransferase 2B7 catalyzing the biotransformation of benzidine and an elevated bladder cancer risk for formerly benzidine-exposed workers of the dyestuff industry.UDP-Glucuronyltransferase 2B7 (UGT2B7) is involved in benzidine metabolism, as demonstrated by in vitro experiments with liver slices. To evaluate the possible association of UGT2B7 gene polymorphism with bladder cancer risk for benzidine-exposed subjects, diagnosed bladder cancer cases (n = 36) who were members of a cohort of benzidine-exposed workers in the Chinese dyestuff industry were investigated. UGT2B7 polymorphism at locus C802T (His268Tyr) was detected using a PCR-RFLP based procedure. Nondiseased cohort members (156 men, 95 women) were taken as work-related control, and unexposed healthy individuals (113 men, 105 women) were taken as community control. The data showed that the polymorphism at locus UGT2B7 C802T in a general Chinese population significantly differs from that in a Caucasian population (p = 0.00018), displaying a distinctly lower frequency of T/T genotypes (9.2 vs. 25.3%), while no significant difference to a Japanese population could be detected (p = 0.17). A higher prevalence of T/T genotype carriers was found in the cancer cases, compared with unexposed healthy controls (25 vs. 9%, odds ratio [OR] 3.30, 95% confidence interval [95% CI] 1.37-7.98, p = 0.006). A higher presentation of T allele carriers in the patients group was also confirmed (46 vs. 33%, OR 1.73, 95% CI 1.05-2.87, p = 0.03). A higher portion of the T/T genotype was also observed in bladder cancer patients compared with nondiseased members of the same benzidine-exposed cohort, although some of them displayed different degrees of cellular alterations in their exfoliated urothelial cells. This study points for the first time to an association between a homozygous mutant genotype of human UDP-glucuronosyltransferase 2B7 catalyzing the biotransformation of benzidine and an elevated bladder cancer risk for formerly benzidine-exposed workers of the dyestuff industry. UDP-Glucuronyltransferase 2B7 (UGT2B7) is involved in benzidine metabolism, as demonstrated by in vitro experiments with liver slices. To evaluate the possible association of UGT2B7 gene polymorphism with bladder cancer risk for benzidine-exposed subjects, diagnosed bladder cancer cases (n = 36) who were members of a cohort of benzidine-exposed workers in the Chinese dyestuff industry were investigated. UGT2B7 polymorphism at locus C802T (His268Tyr) was detected using a PCR-RFLP based procedure. Nondiseased cohort members (156 men, 95 women) were taken as work-related control, and unexposed healthy individuals (113 men, 105 women) were taken as community control. The data showed that the polymorphism at locus UGT2B7 C802T in a general Chinese population significantly differs from that in a Caucasian population (p = 0.00018), displaying a distinctly lower frequency of T/T genotypes (9.2 vs. 25.3%), while no significant difference to a Japanese population could be detected (p = 0.17). A higher prevalence of T/T genotype carriers was found in the cancer cases, compared with unexposed healthy controls (25 vs. 9%, odds ratio [OR] 3.30, 95% confidence interval [95% CI] 1.37–7.98, p = 0.006). A higher presentation of T allele carriers in the patients group was also confirmed (46 vs. 33%, OR 1.73, 95% CI 1.05–2.87, p = 0.03). A higher portion of the T/T genotype was also observed in bladder cancer patients compared with nondiseased members of the same benzidine-exposed cohort, although some of them displayed different degrees of cellular alterations in their exfoliated urothelial cells. This study points for the first time to an association between a homozygous mutant genotype of human UDP-glucuronosyltransferase 2B7 catalyzing the biotransformation of benzidine and an elevated bladder cancer risk for formerly benzidine-exposed workers of the dyestuff industry. |
Author | Lin, Guo-fang Chen, Ji-gang Qin, Yi-qing Ma, Qing-wen Lu, Da-ru Guo, Wei-chao Golka, Klaus Xiang, Cui-qing Shen, Jian-hua |
Author_xml | – sequence: 1 givenname: Guo-fang surname: Lin fullname: Lin, Guo-fang organization: Institute of Plant Physiology and Ecology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200032, China – sequence: 2 givenname: Wei-chao surname: Guo fullname: Guo, Wei-chao organization: Institute of Plant Physiology and Ecology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200032, China – sequence: 3 givenname: Ji-gang surname: Chen fullname: Chen, Ji-gang organization: Municipal Center for Disease Prevention and Control, Shanghai 200236, China – sequence: 4 givenname: Yi-qing surname: Qin fullname: Qin, Yi-qing organization: Municipal Center for Disease Prevention and Control, Shanghai 200236, China – sequence: 5 givenname: Klaus surname: Golka fullname: Golka, Klaus organization: Institute for Occupational Physiology at the University of Dortmund, 44139 Dortmund, Germany; and – sequence: 6 givenname: Cui-qing surname: Xiang fullname: Xiang, Cui-qing organization: Municipal Center for Disease Prevention and Control, Shanghai 200236, China – sequence: 7 givenname: Qing-wen surname: Ma fullname: Ma, Qing-wen organization: Institute of Plant Physiology and Ecology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200032, China – sequence: 8 givenname: Da-ru surname: Lu fullname: Lu, Da-ru organization: Institute of Genetics, Fudan University, Shanghai 200333, China – sequence: 9 givenname: Jian-hua surname: Shen fullname: Shen, Jian-hua email: To whom correspondence should be addressed at Laboratory of Toxicology, Institute of Plant Physiology and Ecology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, 300 Fenglin Road, Shanghai 200032, China. Fax: +86-21-5492-4015. jhshen@sibs.ac.cn. organization: Institute of Plant Physiology and Ecology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200032, China |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/15615884$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1016/j.abb.2004.02.004 10.1126/science.95.2469.438 10.1093/toxsci/kfh068 10.1016/S0140-6736(82)90810-8 10.1097/00008571-200011000-00002 10.1126/science.101.2629.519 10.1016/S0378-4274(01)00544-6 10.1093/carcin/14.12.2637 10.1097/00008571-200307000-00006 10.1016/j.toxlet.2003.11.015 10.2174/1389200013338379 10.5271/sjweh.150 10.1007/s00204-001-0281-y 10.1016/S0009-9236(03)00053-5 10.1007/s002040050528 10.1007/s00228-002-0490-1 10.1124/dmd.31.9.1125 10.1097/00008571-199708000-00001 10.1093/carcin/16.12.3069 10.1016/S0027-5107(02)00149-5 10.1093/carcin/20.10.1963 10.1093/carcin/14.4.675 10.1097/00008571-200308000-00010 10.1179/107735297800407686 10.1097/00008571-200004000-00006 |
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Snippet | UDP-Glucuronyltransferase 2B7 (UGT2B7) is involved in benzidine metabolism, as demonstrated by in vitro experiments with liver slices. To evaluate the possible... |
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SubjectTerms | aromatic amines Asian Continental Ancestry Group - genetics Benzidines - toxicity Carcinoma, Transitional Cell - chemically induced Carcinoma, Transitional Cell - enzymology Carcinoma, Transitional Cell - genetics Chemical Industry China Chinese Cohort Studies Female Gene Frequency Genetic Predisposition to Disease glucuronidation Glucuronosyltransferase - genetics Homozygote Humans Male Occupational Exposure - adverse effects Polymorphism, Genetic transitional cell carcinoma Urinary Bladder Neoplasms - chemically induced Urinary Bladder Neoplasms - enzymology Urinary Bladder Neoplasms - genetics |
Title | An Association of UDP-Glucuronosyltransferase 2B7 C802T (His268Tyr) Polymorphism with Bladder Cancer in Benzidine-Exposed Workers in China |
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