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Case–control study and meta-analysis of SULT1A1 Arg(213)His polymorphism for gene, ethnicity and environment interaction for cancer risk

Cytosolic sulphotransferase SULT1A1 plays a dual role in the activation of some carcinogens and inactivation of others. A functional polymorphism leading to Arg(213)His substitution (SULT1A1*2) affects its catalytic activity and thermostability. To study the association of SULT1A1*2 polymorphism wit...

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Autores principales: Kotnis, A, Kannan, S, Sarin, R, Mulherkar, R
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2570530/
https://www.ncbi.nlm.nih.gov/pubmed/18854828
http://dx.doi.org/10.1038/sj.bjc.6604683
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author Kotnis, A
Kannan, S
Sarin, R
Mulherkar, R
author_facet Kotnis, A
Kannan, S
Sarin, R
Mulherkar, R
author_sort Kotnis, A
collection PubMed
description Cytosolic sulphotransferase SULT1A1 plays a dual role in the activation of some carcinogens and inactivation of others. A functional polymorphism leading to Arg(213)His substitution (SULT1A1*2) affects its catalytic activity and thermostability. To study the association of SULT1A1*2 polymorphism with tobacco-related cancers (TRCs), a case–control study comprising 132 patients with multiple primary neoplasm (MPN) involving TRC and 198 cancer-free controls was carried out. One hundred and thirteen MPN patients had at least one cancer in upper aerodigestive tract including lung (UADT-MPN). SULT1A1*2 showed significant risk association with UADT-MPN (odds ratio (OR)=5.50, 95% confidence interval (CI): 1.09, 27.7). Meta-analysis was conducted combining the data with 34 published studies that included 11 962 cancer cases and 14 673 controls in diverse cancers. The SULT1A1*2 revealed contrasting risk association for UADT cancers (OR=1.62, 95% CI: 1.12, 2.34) and genitourinary cancers (OR=0.73, 95% CI: 0.58, 0.92). Furthermore, although SULT1A1*2 conferred significant increased risk of breast cancer to Asian women (OR=1.91, 95% CI: 1.08, 3.40), it did not confer increased risk to Caucasian women (OR=0.92, 95% CI: 0.71, 1.18). Thus risk for different cancers in distinct ethnic groups could be modulated by interaction between genetic variants and different endogenous and exogenous carcinogens.
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spelling pubmed-25705302009-10-21 Case–control study and meta-analysis of SULT1A1 Arg(213)His polymorphism for gene, ethnicity and environment interaction for cancer risk Kotnis, A Kannan, S Sarin, R Mulherkar, R Br J Cancer Genetics and Genomics Cytosolic sulphotransferase SULT1A1 plays a dual role in the activation of some carcinogens and inactivation of others. A functional polymorphism leading to Arg(213)His substitution (SULT1A1*2) affects its catalytic activity and thermostability. To study the association of SULT1A1*2 polymorphism with tobacco-related cancers (TRCs), a case–control study comprising 132 patients with multiple primary neoplasm (MPN) involving TRC and 198 cancer-free controls was carried out. One hundred and thirteen MPN patients had at least one cancer in upper aerodigestive tract including lung (UADT-MPN). SULT1A1*2 showed significant risk association with UADT-MPN (odds ratio (OR)=5.50, 95% confidence interval (CI): 1.09, 27.7). Meta-analysis was conducted combining the data with 34 published studies that included 11 962 cancer cases and 14 673 controls in diverse cancers. The SULT1A1*2 revealed contrasting risk association for UADT cancers (OR=1.62, 95% CI: 1.12, 2.34) and genitourinary cancers (OR=0.73, 95% CI: 0.58, 0.92). Furthermore, although SULT1A1*2 conferred significant increased risk of breast cancer to Asian women (OR=1.91, 95% CI: 1.08, 3.40), it did not confer increased risk to Caucasian women (OR=0.92, 95% CI: 0.71, 1.18). Thus risk for different cancers in distinct ethnic groups could be modulated by interaction between genetic variants and different endogenous and exogenous carcinogens. Nature Publishing Group 2008-10-21 2008-10-14 /pmc/articles/PMC2570530/ /pubmed/18854828 http://dx.doi.org/10.1038/sj.bjc.6604683 Text en Copyright © 2008 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Genetics and Genomics
Kotnis, A
Kannan, S
Sarin, R
Mulherkar, R
Case–control study and meta-analysis of SULT1A1 Arg(213)His polymorphism for gene, ethnicity and environment interaction for cancer risk
title Case–control study and meta-analysis of SULT1A1 Arg(213)His polymorphism for gene, ethnicity and environment interaction for cancer risk
title_full Case–control study and meta-analysis of SULT1A1 Arg(213)His polymorphism for gene, ethnicity and environment interaction for cancer risk
title_fullStr Case–control study and meta-analysis of SULT1A1 Arg(213)His polymorphism for gene, ethnicity and environment interaction for cancer risk
title_full_unstemmed Case–control study and meta-analysis of SULT1A1 Arg(213)His polymorphism for gene, ethnicity and environment interaction for cancer risk
title_short Case–control study and meta-analysis of SULT1A1 Arg(213)His polymorphism for gene, ethnicity and environment interaction for cancer risk
title_sort case–control study and meta-analysis of sult1a1 arg(213)his polymorphism for gene, ethnicity and environment interaction for cancer risk
topic Genetics and Genomics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2570530/
https://www.ncbi.nlm.nih.gov/pubmed/18854828
http://dx.doi.org/10.1038/sj.bjc.6604683
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