The contribution of the ABCG2 C421A polymorphism to cancer susceptibility: a meta-analysis of the current literature

<p>Abstract</p> <p>Background</p> <p>ABCG2, also known as BCRP, is a half ATP-binding cassette (ABC) transporter that localizes to plasma membranes. Recently, a number of studies have investigated the relationship between the C421A polymorphism in ABCG2 and cancer risk...

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Main Authors: Chen Pin, Zhao Lin, Zou Peng, Xu Haitao, Lu Ailin, Zhao Peng
Format: Article
Language:English
Published: BMC 2012-09-01
Series:BMC Cancer
Online Access:http://www.biomedcentral.com/1471-2407/12/383
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author Chen Pin
Zhao Lin
Zou Peng
Xu Haitao
Lu Ailin
Zhao Peng
author_facet Chen Pin
Zhao Lin
Zou Peng
Xu Haitao
Lu Ailin
Zhao Peng
author_sort Chen Pin
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>ABCG2, also known as BCRP, is a half ATP-binding cassette (ABC) transporter that localizes to plasma membranes. Recently, a number of studies have investigated the relationship between the C421A polymorphism in ABCG2 and cancer risk in multiple populations and various types of cancers; however, this relationship remains unclear. Therefore, we performed a meta-analysis to further explore this association.</p> <p>Methods</p> <p>The meta-analysis incorporated 10 studies involving a total of 3593 cases and 5875 controls. Odds ratios (ORs) and 95% confidence intervals (CIs) were calculated based on the date extracted from the studies to evaluate the strength of association. We also analyzed the heterogeneity and sensitivity of each report and the publication bias of the studies.</p> <p>Results</p> <p>Overall, our results showed that there appeared to be a significant association between the ABCG2 C421A polymorphism and decreased cancer susceptibility (heterozygote-AC versus CC: OR = 0.759, 95%CI = 0.620-0.930; dominant effects model-AA/AC versus CC: OR = 0.771, 95%CI = 0.634-0.938; additive effects model-A allele versus C allele: OR = 0.809, 95%CI = 0.687-0.952). Similarly, decreased cancer risk was also found after stratification of the SNP data by cancer type, ethnicity and source of controls in heterozygote model, dominant effects model and additive effects model.</p> <p>Conclusions</p> <p>We found that the ABCG2 C421A polymorphism is a protective factor for developing cancer. The same relationship was found when the studies were stratified by cancer type, ethnicity and source of controls.</p>
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spelling doaj.art-c2eb135432c14a26b5d990a4aea847132022-12-22T01:42:05ZengBMCBMC Cancer1471-24072012-09-0112138310.1186/1471-2407-12-383The contribution of the ABCG2 C421A polymorphism to cancer susceptibility: a meta-analysis of the current literatureChen PinZhao LinZou PengXu HaitaoLu AilinZhao Peng<p>Abstract</p> <p>Background</p> <p>ABCG2, also known as BCRP, is a half ATP-binding cassette (ABC) transporter that localizes to plasma membranes. Recently, a number of studies have investigated the relationship between the C421A polymorphism in ABCG2 and cancer risk in multiple populations and various types of cancers; however, this relationship remains unclear. Therefore, we performed a meta-analysis to further explore this association.</p> <p>Methods</p> <p>The meta-analysis incorporated 10 studies involving a total of 3593 cases and 5875 controls. Odds ratios (ORs) and 95% confidence intervals (CIs) were calculated based on the date extracted from the studies to evaluate the strength of association. We also analyzed the heterogeneity and sensitivity of each report and the publication bias of the studies.</p> <p>Results</p> <p>Overall, our results showed that there appeared to be a significant association between the ABCG2 C421A polymorphism and decreased cancer susceptibility (heterozygote-AC versus CC: OR = 0.759, 95%CI = 0.620-0.930; dominant effects model-AA/AC versus CC: OR = 0.771, 95%CI = 0.634-0.938; additive effects model-A allele versus C allele: OR = 0.809, 95%CI = 0.687-0.952). Similarly, decreased cancer risk was also found after stratification of the SNP data by cancer type, ethnicity and source of controls in heterozygote model, dominant effects model and additive effects model.</p> <p>Conclusions</p> <p>We found that the ABCG2 C421A polymorphism is a protective factor for developing cancer. The same relationship was found when the studies were stratified by cancer type, ethnicity and source of controls.</p>http://www.biomedcentral.com/1471-2407/12/383
spellingShingle Chen Pin
Zhao Lin
Zou Peng
Xu Haitao
Lu Ailin
Zhao Peng
The contribution of the ABCG2 C421A polymorphism to cancer susceptibility: a meta-analysis of the current literature
BMC Cancer
title The contribution of the ABCG2 C421A polymorphism to cancer susceptibility: a meta-analysis of the current literature
title_full The contribution of the ABCG2 C421A polymorphism to cancer susceptibility: a meta-analysis of the current literature
title_fullStr The contribution of the ABCG2 C421A polymorphism to cancer susceptibility: a meta-analysis of the current literature
title_full_unstemmed The contribution of the ABCG2 C421A polymorphism to cancer susceptibility: a meta-analysis of the current literature
title_short The contribution of the ABCG2 C421A polymorphism to cancer susceptibility: a meta-analysis of the current literature
title_sort contribution of the abcg2 c421a polymorphism to cancer susceptibility a meta analysis of the current literature
url http://www.biomedcentral.com/1471-2407/12/383
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