Cargando…

Mitogen-Activated Protein Kinase Kinase 4 Gene Polymorphism and Cancer Risk

A number of epidemiological studies have assessed the association of −1304T > G polymorphism in the MKK4 gene and risk of cancer, but the results lack of statistical power due to the limited subjects used in these studies. This study was devised to identify the genetic effects of the −1304T > ...

Descripción completa

Detalles Bibliográficos
Autores principales: Geng, Peiliang, Ou, Juanjuan, Xie, Ganfeng, Li, Jianjun, Zhao, Xiaoxin, Xiang, Lisha, Liao, Yunmei, Wang, Ning, Liang, Houjie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4915862/
https://www.ncbi.nlm.nih.gov/pubmed/26554761
http://dx.doi.org/10.1097/MD.0000000000000938
_version_ 1782438744650940416
author Geng, Peiliang
Ou, Juanjuan
Xie, Ganfeng
Li, Jianjun
Zhao, Xiaoxin
Xiang, Lisha
Liao, Yunmei
Wang, Ning
Liang, Houjie
author_facet Geng, Peiliang
Ou, Juanjuan
Xie, Ganfeng
Li, Jianjun
Zhao, Xiaoxin
Xiang, Lisha
Liao, Yunmei
Wang, Ning
Liang, Houjie
author_sort Geng, Peiliang
collection PubMed
description A number of epidemiological studies have assessed the association of −1304T > G polymorphism in the MKK4 gene and risk of cancer, but the results lack of statistical power due to the limited subjects used in these studies. This study was devised to identify the genetic effects of the −1304T > G polymorphism on cancer risk in a large meta-analysis. Eligible studies were identified by searching both Chinese and English databases. General as well as subgroup analyses were performed for 8 independent case–control publications with a total of 4623 cases and 5256 cancer-free controls. Odds ratios (ORs) and 95% confidence intervals (CIs) were used to estimate the association. Overall, this meta-analysis showed that the association between the −1304T > G polymorphism and cancer risk was statistically significant (GG vs TT: OR = 0.63, 95% CI, 0.52–0.75; GG + TG vs TT: OR = 0.85, 95% CI, 0.79–0.91; GG vs TG + TT: OR = 0.67, 95% CI, 0.56–0.80; G vs T: OR = 0.82, 95% CI, 0.77–0.88; TG vs TT: OR = 0.86, 95% CI, 0.79–0.93). Our meta-analysis reveals that the presence of the −1304T > G polymorphism is likely to decrease risk of cancer. Future larger studies are necessary to validate the current finding.
format Online
Article
Text
id pubmed-4915862
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Wolters Kluwer Health
record_format MEDLINE/PubMed
spelling pubmed-49158622016-07-05 Mitogen-Activated Protein Kinase Kinase 4 Gene Polymorphism and Cancer Risk Geng, Peiliang Ou, Juanjuan Xie, Ganfeng Li, Jianjun Zhao, Xiaoxin Xiang, Lisha Liao, Yunmei Wang, Ning Liang, Houjie Medicine (Baltimore) 5700 A number of epidemiological studies have assessed the association of −1304T > G polymorphism in the MKK4 gene and risk of cancer, but the results lack of statistical power due to the limited subjects used in these studies. This study was devised to identify the genetic effects of the −1304T > G polymorphism on cancer risk in a large meta-analysis. Eligible studies were identified by searching both Chinese and English databases. General as well as subgroup analyses were performed for 8 independent case–control publications with a total of 4623 cases and 5256 cancer-free controls. Odds ratios (ORs) and 95% confidence intervals (CIs) were used to estimate the association. Overall, this meta-analysis showed that the association between the −1304T > G polymorphism and cancer risk was statistically significant (GG vs TT: OR = 0.63, 95% CI, 0.52–0.75; GG + TG vs TT: OR = 0.85, 95% CI, 0.79–0.91; GG vs TG + TT: OR = 0.67, 95% CI, 0.56–0.80; G vs T: OR = 0.82, 95% CI, 0.77–0.88; TG vs TT: OR = 0.86, 95% CI, 0.79–0.93). Our meta-analysis reveals that the presence of the −1304T > G polymorphism is likely to decrease risk of cancer. Future larger studies are necessary to validate the current finding. Wolters Kluwer Health 2015-11-06 /pmc/articles/PMC4915862/ /pubmed/26554761 http://dx.doi.org/10.1097/MD.0000000000000938 Text en Copyright © 2015 Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0
spellingShingle 5700
Geng, Peiliang
Ou, Juanjuan
Xie, Ganfeng
Li, Jianjun
Zhao, Xiaoxin
Xiang, Lisha
Liao, Yunmei
Wang, Ning
Liang, Houjie
Mitogen-Activated Protein Kinase Kinase 4 Gene Polymorphism and Cancer Risk
title Mitogen-Activated Protein Kinase Kinase 4 Gene Polymorphism and Cancer Risk
title_full Mitogen-Activated Protein Kinase Kinase 4 Gene Polymorphism and Cancer Risk
title_fullStr Mitogen-Activated Protein Kinase Kinase 4 Gene Polymorphism and Cancer Risk
title_full_unstemmed Mitogen-Activated Protein Kinase Kinase 4 Gene Polymorphism and Cancer Risk
title_short Mitogen-Activated Protein Kinase Kinase 4 Gene Polymorphism and Cancer Risk
title_sort mitogen-activated protein kinase kinase 4 gene polymorphism and cancer risk
topic 5700
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4915862/
https://www.ncbi.nlm.nih.gov/pubmed/26554761
http://dx.doi.org/10.1097/MD.0000000000000938
work_keys_str_mv AT gengpeiliang mitogenactivatedproteinkinasekinase4genepolymorphismandcancerrisk
AT oujuanjuan mitogenactivatedproteinkinasekinase4genepolymorphismandcancerrisk
AT xieganfeng mitogenactivatedproteinkinasekinase4genepolymorphismandcancerrisk
AT lijianjun mitogenactivatedproteinkinasekinase4genepolymorphismandcancerrisk
AT zhaoxiaoxin mitogenactivatedproteinkinasekinase4genepolymorphismandcancerrisk
AT xianglisha mitogenactivatedproteinkinasekinase4genepolymorphismandcancerrisk
AT liaoyunmei mitogenactivatedproteinkinasekinase4genepolymorphismandcancerrisk
AT wangning mitogenactivatedproteinkinasekinase4genepolymorphismandcancerrisk
AT lianghoujie mitogenactivatedproteinkinasekinase4genepolymorphismandcancerrisk