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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...
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/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. |
format | Online Article Text |
id | pubmed-3928286 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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