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Association between CYP17 T-34C rs743572 and breast cancer risk
Association between CYP17 T-34C (rs743572) polymorphism and breast cancer (BC) risk was controversial. In order to derive a more definitive conclusion, we performed this meta-analysis. We searched in the databases of PubMed, EMBASE and Cochrane for eligible publications. Pooled odds ratios (ORs) wit...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5790532/ https://www.ncbi.nlm.nih.gov/pubmed/29423115 http://dx.doi.org/10.18632/oncotarget.23688 |
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author | Sun, Jing Zhang, Hong Gao, Meiyan Tang, Zhishu Guo, Dongyan Zhang, Xiaofei Wang, Zhu Li, Ruiping Liu, Yan Sun, Wansen Sun, Xi |
author_facet | Sun, Jing Zhang, Hong Gao, Meiyan Tang, Zhishu Guo, Dongyan Zhang, Xiaofei Wang, Zhu Li, Ruiping Liu, Yan Sun, Wansen Sun, Xi |
author_sort | Sun, Jing |
collection | PubMed |
description | Association between CYP17 T-34C (rs743572) polymorphism and breast cancer (BC) risk was controversial. In order to derive a more definitive conclusion, we performed this meta-analysis. We searched in the databases of PubMed, EMBASE and Cochrane for eligible publications. Pooled odds ratios (ORs) with 95% confidence intervals (95% CIs) were used to assess the strength of association between CYP17 T-34C polymorphism and breast cancer risk. Forty-nine studies involving 2,7104 cases and 3,4218 control subjects were included in this meta-analysis. In overall, no significant association between CYP17 T-34C polymorphism and breast cancer susceptibility was found among general populations. In the stratified analysis by ethnicity and source, significant associations were still not detected in all genetic models; besides, limiting the analysis to studies with controls in agreement with HWE, we also observed no association between CYP17 T-34C polymorphism and breast cancer risk. For premenopausal women, we didn't detect an association between rs743572 and breast cancer risk; however, among postmenopausal women, we observed that the association was statistically significant under the allele contrast genetic model (OR = 1.10, 95% CI = 1.03–1.17, P = 0.003), but not in other four models. In conclusion, rs743572 may increase breast cancer risk in postmenopausal individuals, but not in premenopausal folks and general populations. |
format | Online Article Text |
id | pubmed-5790532 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-57905322018-02-08 Association between CYP17 T-34C rs743572 and breast cancer risk Sun, Jing Zhang, Hong Gao, Meiyan Tang, Zhishu Guo, Dongyan Zhang, Xiaofei Wang, Zhu Li, Ruiping Liu, Yan Sun, Wansen Sun, Xi Oncotarget Research Paper Association between CYP17 T-34C (rs743572) polymorphism and breast cancer (BC) risk was controversial. In order to derive a more definitive conclusion, we performed this meta-analysis. We searched in the databases of PubMed, EMBASE and Cochrane for eligible publications. Pooled odds ratios (ORs) with 95% confidence intervals (95% CIs) were used to assess the strength of association between CYP17 T-34C polymorphism and breast cancer risk. Forty-nine studies involving 2,7104 cases and 3,4218 control subjects were included in this meta-analysis. In overall, no significant association between CYP17 T-34C polymorphism and breast cancer susceptibility was found among general populations. In the stratified analysis by ethnicity and source, significant associations were still not detected in all genetic models; besides, limiting the analysis to studies with controls in agreement with HWE, we also observed no association between CYP17 T-34C polymorphism and breast cancer risk. For premenopausal women, we didn't detect an association between rs743572 and breast cancer risk; however, among postmenopausal women, we observed that the association was statistically significant under the allele contrast genetic model (OR = 1.10, 95% CI = 1.03–1.17, P = 0.003), but not in other four models. In conclusion, rs743572 may increase breast cancer risk in postmenopausal individuals, but not in premenopausal folks and general populations. Impact Journals LLC 2017-12-26 /pmc/articles/PMC5790532/ /pubmed/29423115 http://dx.doi.org/10.18632/oncotarget.23688 Text en Copyright: © 2018 Sun et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Sun, Jing Zhang, Hong Gao, Meiyan Tang, Zhishu Guo, Dongyan Zhang, Xiaofei Wang, Zhu Li, Ruiping Liu, Yan Sun, Wansen Sun, Xi Association between CYP17 T-34C rs743572 and breast cancer risk |
title | Association between CYP17 T-34C rs743572 and breast cancer risk |
title_full | Association between CYP17 T-34C rs743572 and breast cancer risk |
title_fullStr | Association between CYP17 T-34C rs743572 and breast cancer risk |
title_full_unstemmed | Association between CYP17 T-34C rs743572 and breast cancer risk |
title_short | Association between CYP17 T-34C rs743572 and breast cancer risk |
title_sort | association between cyp17 t-34c rs743572 and breast cancer risk |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5790532/ https://www.ncbi.nlm.nih.gov/pubmed/29423115 http://dx.doi.org/10.18632/oncotarget.23688 |
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