Cargando…
PAI-1 promoter 4G/5G polymorphism (rs1799768) contributes to tumor susceptibility: Evidence from meta-analysis
Plasminogen activator inhibitor-1 (PAI-1), belonging to the urokinase plasminogen activation (uPA) system, is involved in cancer development and progression. The PAI-1 promoter 4G/5G polymorphism was shown to contribute to genetic susceptibility to cancer, although the results were inconsistent. To...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3494103/ https://www.ncbi.nlm.nih.gov/pubmed/23226787 http://dx.doi.org/10.3892/etm.2012.734 |
_version_ | 1782249360217604096 |
---|---|
author | XU, XIN XIE, YANQI LIN, YIWEI XU, XIANGLAI ZHU, YI MAO, YEQING HU, ZHENGHUI WU, JIAN CHEN, HONG ZHENG, XIANGYI QIN, JIE XIE, LIPING |
author_facet | XU, XIN XIE, YANQI LIN, YIWEI XU, XIANGLAI ZHU, YI MAO, YEQING HU, ZHENGHUI WU, JIAN CHEN, HONG ZHENG, XIANGYI QIN, JIE XIE, LIPING |
author_sort | XU, XIN |
collection | PubMed |
description | Plasminogen activator inhibitor-1 (PAI-1), belonging to the urokinase plasminogen activation (uPA) system, is involved in cancer development and progression. The PAI-1 promoter 4G/5G polymorphism was shown to contribute to genetic susceptibility to cancer, although the results were inconsistent. To assess this relationship more precisely, a meta-analysis was performed. The electronic databases PubMed, Scopus, Web of Science and Chinese National Knowledge Infrastructure (CNKI) were searched; data were extracted and analyzed independently by two reviewers. Ultimately, 21 eligible case-control studies with a total of 8,415 cancer cases and 9,208 controls were included. The overall odds ratio (OR) with its 95% confidence interval (CI) showed a statistically significant association between the PAI-1 promoter 4G/5G polymorphism and cancer risk (4G/4G vs. 5G/5G: OR=1.25, 95% CI=1.07–1.47, P(heterogeneity)=0.001; 4G/4G vs. 4G/5G+5G/5G: OR=1.10, 95% CI=1.03–1.17, P(heterogeneity)=0.194; 4G/4G+4G/5G vs. 5G/5G: OR=1.17, 95% CI=1.01–1.35, P(heterogeneity)=0.041). In further subgroup analyses, the increased risk of cancer was observed in a subgroup of Caucasians with regards to endometrial cancer. Our meta-analysis suggests that the PAI-1 4G/5G polymorphism most likely contributes to susceptibility to cancer, particularly in Caucasians. Furthermore, the 4G allele may be associated with an increased risk of endometrial cancer. |
format | Online Article Text |
id | pubmed-3494103 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-34941032012-12-06 PAI-1 promoter 4G/5G polymorphism (rs1799768) contributes to tumor susceptibility: Evidence from meta-analysis XU, XIN XIE, YANQI LIN, YIWEI XU, XIANGLAI ZHU, YI MAO, YEQING HU, ZHENGHUI WU, JIAN CHEN, HONG ZHENG, XIANGYI QIN, JIE XIE, LIPING Exp Ther Med Articles Plasminogen activator inhibitor-1 (PAI-1), belonging to the urokinase plasminogen activation (uPA) system, is involved in cancer development and progression. The PAI-1 promoter 4G/5G polymorphism was shown to contribute to genetic susceptibility to cancer, although the results were inconsistent. To assess this relationship more precisely, a meta-analysis was performed. The electronic databases PubMed, Scopus, Web of Science and Chinese National Knowledge Infrastructure (CNKI) were searched; data were extracted and analyzed independently by two reviewers. Ultimately, 21 eligible case-control studies with a total of 8,415 cancer cases and 9,208 controls were included. The overall odds ratio (OR) with its 95% confidence interval (CI) showed a statistically significant association between the PAI-1 promoter 4G/5G polymorphism and cancer risk (4G/4G vs. 5G/5G: OR=1.25, 95% CI=1.07–1.47, P(heterogeneity)=0.001; 4G/4G vs. 4G/5G+5G/5G: OR=1.10, 95% CI=1.03–1.17, P(heterogeneity)=0.194; 4G/4G+4G/5G vs. 5G/5G: OR=1.17, 95% CI=1.01–1.35, P(heterogeneity)=0.041). In further subgroup analyses, the increased risk of cancer was observed in a subgroup of Caucasians with regards to endometrial cancer. Our meta-analysis suggests that the PAI-1 4G/5G polymorphism most likely contributes to susceptibility to cancer, particularly in Caucasians. Furthermore, the 4G allele may be associated with an increased risk of endometrial cancer. D.A. Spandidos 2012-12 2012-10-02 /pmc/articles/PMC3494103/ /pubmed/23226787 http://dx.doi.org/10.3892/etm.2012.734 Text en Copyright © 2012, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited. |
spellingShingle | Articles XU, XIN XIE, YANQI LIN, YIWEI XU, XIANGLAI ZHU, YI MAO, YEQING HU, ZHENGHUI WU, JIAN CHEN, HONG ZHENG, XIANGYI QIN, JIE XIE, LIPING PAI-1 promoter 4G/5G polymorphism (rs1799768) contributes to tumor susceptibility: Evidence from meta-analysis |
title | PAI-1 promoter 4G/5G polymorphism (rs1799768) contributes to tumor susceptibility: Evidence from meta-analysis |
title_full | PAI-1 promoter 4G/5G polymorphism (rs1799768) contributes to tumor susceptibility: Evidence from meta-analysis |
title_fullStr | PAI-1 promoter 4G/5G polymorphism (rs1799768) contributes to tumor susceptibility: Evidence from meta-analysis |
title_full_unstemmed | PAI-1 promoter 4G/5G polymorphism (rs1799768) contributes to tumor susceptibility: Evidence from meta-analysis |
title_short | PAI-1 promoter 4G/5G polymorphism (rs1799768) contributes to tumor susceptibility: Evidence from meta-analysis |
title_sort | pai-1 promoter 4g/5g polymorphism (rs1799768) contributes to tumor susceptibility: evidence from meta-analysis |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3494103/ https://www.ncbi.nlm.nih.gov/pubmed/23226787 http://dx.doi.org/10.3892/etm.2012.734 |
work_keys_str_mv | AT xuxin pai1promoter4g5gpolymorphismrs1799768contributestotumorsusceptibilityevidencefrommetaanalysis AT xieyanqi pai1promoter4g5gpolymorphismrs1799768contributestotumorsusceptibilityevidencefrommetaanalysis AT linyiwei pai1promoter4g5gpolymorphismrs1799768contributestotumorsusceptibilityevidencefrommetaanalysis AT xuxianglai pai1promoter4g5gpolymorphismrs1799768contributestotumorsusceptibilityevidencefrommetaanalysis AT zhuyi pai1promoter4g5gpolymorphismrs1799768contributestotumorsusceptibilityevidencefrommetaanalysis AT maoyeqing pai1promoter4g5gpolymorphismrs1799768contributestotumorsusceptibilityevidencefrommetaanalysis AT huzhenghui pai1promoter4g5gpolymorphismrs1799768contributestotumorsusceptibilityevidencefrommetaanalysis AT wujian pai1promoter4g5gpolymorphismrs1799768contributestotumorsusceptibilityevidencefrommetaanalysis AT chenhong pai1promoter4g5gpolymorphismrs1799768contributestotumorsusceptibilityevidencefrommetaanalysis AT zhengxiangyi pai1promoter4g5gpolymorphismrs1799768contributestotumorsusceptibilityevidencefrommetaanalysis AT qinjie pai1promoter4g5gpolymorphismrs1799768contributestotumorsusceptibilityevidencefrommetaanalysis AT xieliping pai1promoter4g5gpolymorphismrs1799768contributestotumorsusceptibilityevidencefrommetaanalysis |