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Association of mTOR Polymorphisms with Cancer Risk and Clinical Outcomes: A Meta-Analysis
Genetic polymorphisms in mTOR gene may be associated with cancer risk and clinical outcomes of cancer patients by affecting mTOR gene expression or its activation. However, inconsistent results have been reported. The aim of this study is to systematically evaluate the association between mTOR polym...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4016248/ https://www.ncbi.nlm.nih.gov/pubmed/24816861 http://dx.doi.org/10.1371/journal.pone.0097085 |
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author | Shao, Jianbo Li, Ying Zhao, Peiwei Yue, Xin Jiang, Jun Liang, Xiaohui He, Xuelian |
author_facet | Shao, Jianbo Li, Ying Zhao, Peiwei Yue, Xin Jiang, Jun Liang, Xiaohui He, Xuelian |
author_sort | Shao, Jianbo |
collection | PubMed |
description | Genetic polymorphisms in mTOR gene may be associated with cancer risk and clinical outcomes of cancer patients by affecting mTOR gene expression or its activation. However, inconsistent results have been reported. The aim of this study is to systematically evaluate the association between mTOR polymorphisms (rs2295080, rs2536 and rs11121704) and cancer risk as well as clinical outcome by a meta-analysis. We identified 10 eligible studies and extracted data by two investigators. Based on dominant and recessive models, odds ratio (ORs) and 95% confidence intervals (CIs) were calculated by using Stata, version 11 to evaluate the association strength. Our meta-analysis results showed that the wild genotype TT of rs2295080 polymorphism was associated with increased cancer risk under dominant model (OR = 1.24, 95%CI: 1.12–1.36, p<0.0005) in Chinese but not with clinical outcome parameters, while the TT genotype of rs11121704 was associated with poor clinical outcome parameters (OR = 1.53, 95%CI: 1.01–2.32, p = 0.044), such as death, metastasis and resistance to chemotherapy. However, rs2536 may not influence cancer susceptibility. In conclusion, this meta-analysis indicated the common polymorphisms in mTOR gene might be genetic risk factors for the carcinogenesis and clinical outcomes of cancer patients. However, further investigation on large population and different ethnicities are warranted. |
format | Online Article Text |
id | pubmed-4016248 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-40162482014-05-14 Association of mTOR Polymorphisms with Cancer Risk and Clinical Outcomes: A Meta-Analysis Shao, Jianbo Li, Ying Zhao, Peiwei Yue, Xin Jiang, Jun Liang, Xiaohui He, Xuelian PLoS One Research Article Genetic polymorphisms in mTOR gene may be associated with cancer risk and clinical outcomes of cancer patients by affecting mTOR gene expression or its activation. However, inconsistent results have been reported. The aim of this study is to systematically evaluate the association between mTOR polymorphisms (rs2295080, rs2536 and rs11121704) and cancer risk as well as clinical outcome by a meta-analysis. We identified 10 eligible studies and extracted data by two investigators. Based on dominant and recessive models, odds ratio (ORs) and 95% confidence intervals (CIs) were calculated by using Stata, version 11 to evaluate the association strength. Our meta-analysis results showed that the wild genotype TT of rs2295080 polymorphism was associated with increased cancer risk under dominant model (OR = 1.24, 95%CI: 1.12–1.36, p<0.0005) in Chinese but not with clinical outcome parameters, while the TT genotype of rs11121704 was associated with poor clinical outcome parameters (OR = 1.53, 95%CI: 1.01–2.32, p = 0.044), such as death, metastasis and resistance to chemotherapy. However, rs2536 may not influence cancer susceptibility. In conclusion, this meta-analysis indicated the common polymorphisms in mTOR gene might be genetic risk factors for the carcinogenesis and clinical outcomes of cancer patients. However, further investigation on large population and different ethnicities are warranted. Public Library of Science 2014-05-09 /pmc/articles/PMC4016248/ /pubmed/24816861 http://dx.doi.org/10.1371/journal.pone.0097085 Text en © 2014 Shao et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Shao, Jianbo Li, Ying Zhao, Peiwei Yue, Xin Jiang, Jun Liang, Xiaohui He, Xuelian Association of mTOR Polymorphisms with Cancer Risk and Clinical Outcomes: A Meta-Analysis |
title | Association of mTOR Polymorphisms with Cancer Risk and Clinical Outcomes: A Meta-Analysis |
title_full | Association of mTOR Polymorphisms with Cancer Risk and Clinical Outcomes: A Meta-Analysis |
title_fullStr | Association of mTOR Polymorphisms with Cancer Risk and Clinical Outcomes: A Meta-Analysis |
title_full_unstemmed | Association of mTOR Polymorphisms with Cancer Risk and Clinical Outcomes: A Meta-Analysis |
title_short | Association of mTOR Polymorphisms with Cancer Risk and Clinical Outcomes: A Meta-Analysis |
title_sort | association of mtor polymorphisms with cancer risk and clinical outcomes: a meta-analysis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4016248/ https://www.ncbi.nlm.nih.gov/pubmed/24816861 http://dx.doi.org/10.1371/journal.pone.0097085 |
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