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Association of Fas -1377 G/A Polymorphism with Susceptibility to Cancer

BACKGROUND: The relationship between Fas -1377 G/A polymorphism and cancer susceptibility has been implicated in accumulating data. However, the data presented inconsistent results. This study was devised to investigate the association of Fas -1377 G/A polymorphism and cancer susceptibility in a lar...

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Autores principales: Geng, Peiliang, Li, Jianjun, Ou, Juanjuan, Xie, Ganfeng, Wang, Ning, Xiang, Lisha, Sa, Rina, Liu, Chen, Li, Hongtao, Liang, Houjie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3928286/
https://www.ncbi.nlm.nih.gov/pubmed/24558420
http://dx.doi.org/10.1371/journal.pone.0088748
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author Geng, Peiliang
Li, Jianjun
Ou, Juanjuan
Xie, Ganfeng
Wang, Ning
Xiang, Lisha
Sa, Rina
Liu, Chen
Li, Hongtao
Liang, Houjie
author_facet Geng, Peiliang
Li, Jianjun
Ou, Juanjuan
Xie, Ganfeng
Wang, Ning
Xiang, Lisha
Sa, Rina
Liu, Chen
Li, Hongtao
Liang, Houjie
author_sort Geng, Peiliang
collection PubMed
description BACKGROUND: The relationship between Fas -1377 G/A polymorphism and cancer susceptibility has been implicated in accumulating data. However, the data presented inconsistent results. This study was devised to investigate the association of Fas -1377 G/A polymorphism and cancer susceptibility in a large number of participants. METHODS: The databases of PubMed, Embase, and Web of Science were searched and a total of 27 case-control studies including 13,355 cases and 16,078 controls were included in this meta-analysis. Pooled odds ratios (ORs) with 95% confidence intervals (CIs) were calculated using the fixed-effects model. Statistical analyses were performed by using Stata software. RESULTS: The results suggested that Fas -1377 G/A polymorphism was overall associated with cancer susceptibility (additive model: OR, 1.16, 95%CI = 1.06–1.27, P (heterogeneity)  = 0.381; recessive model: OR, 1.19, 95%CI = 1.10–1.29, P (heterogeneity)  = 0.137). In the subgroup analysis by cancer type, significantly increased risk was observed in breast cancer (additive model: OR, 1.24, 95%CI = 1.04–1.58, P (heterogeneity)  = 0.614; recessive model: OR, 1.24, 95%CI = 1.02–1.51, P (heterogeneity)  = 0.349) and lung cancer (recessive model: OR, 1.25, 95%CI = 1.04–1.49, P (heterogeneity)  = 0.090). Similarly, elevated cancer risk associated with Fas -1377 G/A polymorphism was revealed in Asians. CONCLUSIONS: The combined results suggest that Fas -1377 G/A polymorphism might modulate cancer susceptibility in an Asian-specific manner.
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spelling pubmed-39282862014-02-20 Association of Fas -1377 G/A Polymorphism with Susceptibility to Cancer Geng, Peiliang Li, Jianjun Ou, Juanjuan Xie, Ganfeng Wang, Ning Xiang, Lisha Sa, Rina Liu, Chen Li, Hongtao Liang, Houjie PLoS One Research Article BACKGROUND: The relationship between Fas -1377 G/A polymorphism and cancer susceptibility has been implicated in accumulating data. However, the data presented inconsistent results. This study was devised to investigate the association of Fas -1377 G/A polymorphism and cancer susceptibility in a large number of participants. METHODS: The databases of PubMed, Embase, and Web of Science were searched and a total of 27 case-control studies including 13,355 cases and 16,078 controls were included in this meta-analysis. Pooled odds ratios (ORs) with 95% confidence intervals (CIs) were calculated using the fixed-effects model. Statistical analyses were performed by using Stata software. RESULTS: The results suggested that Fas -1377 G/A polymorphism was overall associated with cancer susceptibility (additive model: OR, 1.16, 95%CI = 1.06–1.27, P (heterogeneity)  = 0.381; recessive model: OR, 1.19, 95%CI = 1.10–1.29, P (heterogeneity)  = 0.137). In the subgroup analysis by cancer type, significantly increased risk was observed in breast cancer (additive model: OR, 1.24, 95%CI = 1.04–1.58, P (heterogeneity)  = 0.614; recessive model: OR, 1.24, 95%CI = 1.02–1.51, P (heterogeneity)  = 0.349) and lung cancer (recessive model: OR, 1.25, 95%CI = 1.04–1.49, P (heterogeneity)  = 0.090). Similarly, elevated cancer risk associated with Fas -1377 G/A polymorphism was revealed in Asians. CONCLUSIONS: The combined results suggest that Fas -1377 G/A polymorphism might modulate cancer susceptibility in an Asian-specific manner. Public Library of Science 2014-02-18 /pmc/articles/PMC3928286/ /pubmed/24558420 http://dx.doi.org/10.1371/journal.pone.0088748 Text en © 2014 Geng 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
Geng, Peiliang
Li, Jianjun
Ou, Juanjuan
Xie, Ganfeng
Wang, Ning
Xiang, Lisha
Sa, Rina
Liu, Chen
Li, Hongtao
Liang, Houjie
Association of Fas -1377 G/A Polymorphism with Susceptibility to Cancer
title Association of Fas -1377 G/A Polymorphism with Susceptibility to Cancer
title_full Association of Fas -1377 G/A Polymorphism with Susceptibility to Cancer
title_fullStr Association of Fas -1377 G/A Polymorphism with Susceptibility to Cancer
title_full_unstemmed Association of Fas -1377 G/A Polymorphism with Susceptibility to Cancer
title_short Association of Fas -1377 G/A Polymorphism with Susceptibility to Cancer
title_sort association of fas -1377 g/a polymorphism with susceptibility to cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3928286/
https://www.ncbi.nlm.nih.gov/pubmed/24558420
http://dx.doi.org/10.1371/journal.pone.0088748
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