Cargando…

The rs2233678 Polymorphism in PIN1 Promoter Region Reduced Cancer Risk: A Meta-Analysis

BACKGROUND: Published evidence suggests that the rs2233678 (−842 G>C) polymorphism in the PIN1 (peptidyl-prolyl cis/trans somerase NIMA-interacting 1) promoter region may be associated with cancer risk; however, the conclusion is still inconclusive. METHODS: We conducted a meta-analysis to determ...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Qi, Dong, Zhao, Lin, Yun, Jia, Xinyan, Li, Qun, Jiang, Hong, Wang, Liwei, Gao, Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3706536/
https://www.ncbi.nlm.nih.gov/pubmed/23874525
http://dx.doi.org/10.1371/journal.pone.0068148
_version_ 1782476569688670208
author Li, Qi
Dong, Zhao
Lin, Yun
Jia, Xinyan
Li, Qun
Jiang, Hong
Wang, Liwei
Gao, Yong
author_facet Li, Qi
Dong, Zhao
Lin, Yun
Jia, Xinyan
Li, Qun
Jiang, Hong
Wang, Liwei
Gao, Yong
author_sort Li, Qi
collection PubMed
description BACKGROUND: Published evidence suggests that the rs2233678 (−842 G>C) polymorphism in the PIN1 (peptidyl-prolyl cis/trans somerase NIMA-interacting 1) promoter region may be associated with cancer risk; however, the conclusion is still inconclusive. METHODS: We conducted a meta-analysis to determine whether −842 G>C polymorphism was associated with cancer risk. Odds ratio (OR) and 95% confidence intervals (95% CI) were used to assess the strength of association. Genotype distribution data and adjusted ORs were collected to calculate the pooled ORs. Meta-regression was conducted to detect the source of heterogeneity. Publication bias was evaluated by Egger’s test and Begg’s test. RESULTS: A total of 11 eligible studies, including 9280 participants, were identified and analyzed. Overall, we found that carriers of the −842 C allele were associated with significantly decreased cancer risk (C vs. G, OR = 0.750, 95% CI: 0.639–0.880, P(heterogeneity) = 0.014, estimated by genotype distribution data; CC+GC vs. GG, OR = 0.668, 95% CI: 0.594–0.751, P(heterogeneity) = 0.638, estimated by adjusted ORs). No evidence of publication bias was observed. Meta-regression revealed that ethnicities (p = 0.021) and sample size (p = 0.02) but not sources of control (p = 0.069) were the source of heterogeneity. CONCLUSION: These results suggest that the PIN1 rs2233678 (−842 G>C) polymorphism significantly reduces cancer risk.
format Online
Article
Text
id pubmed-3706536
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-37065362013-07-19 The rs2233678 Polymorphism in PIN1 Promoter Region Reduced Cancer Risk: A Meta-Analysis Li, Qi Dong, Zhao Lin, Yun Jia, Xinyan Li, Qun Jiang, Hong Wang, Liwei Gao, Yong PLoS One Research Article BACKGROUND: Published evidence suggests that the rs2233678 (−842 G>C) polymorphism in the PIN1 (peptidyl-prolyl cis/trans somerase NIMA-interacting 1) promoter region may be associated with cancer risk; however, the conclusion is still inconclusive. METHODS: We conducted a meta-analysis to determine whether −842 G>C polymorphism was associated with cancer risk. Odds ratio (OR) and 95% confidence intervals (95% CI) were used to assess the strength of association. Genotype distribution data and adjusted ORs were collected to calculate the pooled ORs. Meta-regression was conducted to detect the source of heterogeneity. Publication bias was evaluated by Egger’s test and Begg’s test. RESULTS: A total of 11 eligible studies, including 9280 participants, were identified and analyzed. Overall, we found that carriers of the −842 C allele were associated with significantly decreased cancer risk (C vs. G, OR = 0.750, 95% CI: 0.639–0.880, P(heterogeneity) = 0.014, estimated by genotype distribution data; CC+GC vs. GG, OR = 0.668, 95% CI: 0.594–0.751, P(heterogeneity) = 0.638, estimated by adjusted ORs). No evidence of publication bias was observed. Meta-regression revealed that ethnicities (p = 0.021) and sample size (p = 0.02) but not sources of control (p = 0.069) were the source of heterogeneity. CONCLUSION: These results suggest that the PIN1 rs2233678 (−842 G>C) polymorphism significantly reduces cancer risk. Public Library of Science 2013-07-09 /pmc/articles/PMC3706536/ /pubmed/23874525 http://dx.doi.org/10.1371/journal.pone.0068148 Text en © 2013 Li 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
Li, Qi
Dong, Zhao
Lin, Yun
Jia, Xinyan
Li, Qun
Jiang, Hong
Wang, Liwei
Gao, Yong
The rs2233678 Polymorphism in PIN1 Promoter Region Reduced Cancer Risk: A Meta-Analysis
title The rs2233678 Polymorphism in PIN1 Promoter Region Reduced Cancer Risk: A Meta-Analysis
title_full The rs2233678 Polymorphism in PIN1 Promoter Region Reduced Cancer Risk: A Meta-Analysis
title_fullStr The rs2233678 Polymorphism in PIN1 Promoter Region Reduced Cancer Risk: A Meta-Analysis
title_full_unstemmed The rs2233678 Polymorphism in PIN1 Promoter Region Reduced Cancer Risk: A Meta-Analysis
title_short The rs2233678 Polymorphism in PIN1 Promoter Region Reduced Cancer Risk: A Meta-Analysis
title_sort rs2233678 polymorphism in pin1 promoter region reduced cancer risk: a meta-analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3706536/
https://www.ncbi.nlm.nih.gov/pubmed/23874525
http://dx.doi.org/10.1371/journal.pone.0068148
work_keys_str_mv AT liqi thers2233678polymorphisminpin1promoterregionreducedcancerriskametaanalysis
AT dongzhao thers2233678polymorphisminpin1promoterregionreducedcancerriskametaanalysis
AT linyun thers2233678polymorphisminpin1promoterregionreducedcancerriskametaanalysis
AT jiaxinyan thers2233678polymorphisminpin1promoterregionreducedcancerriskametaanalysis
AT liqun thers2233678polymorphisminpin1promoterregionreducedcancerriskametaanalysis
AT jianghong thers2233678polymorphisminpin1promoterregionreducedcancerriskametaanalysis
AT wangliwei thers2233678polymorphisminpin1promoterregionreducedcancerriskametaanalysis
AT gaoyong thers2233678polymorphisminpin1promoterregionreducedcancerriskametaanalysis
AT liqi rs2233678polymorphisminpin1promoterregionreducedcancerriskametaanalysis
AT dongzhao rs2233678polymorphisminpin1promoterregionreducedcancerriskametaanalysis
AT linyun rs2233678polymorphisminpin1promoterregionreducedcancerriskametaanalysis
AT jiaxinyan rs2233678polymorphisminpin1promoterregionreducedcancerriskametaanalysis
AT liqun rs2233678polymorphisminpin1promoterregionreducedcancerriskametaanalysis
AT jianghong rs2233678polymorphisminpin1promoterregionreducedcancerriskametaanalysis
AT wangliwei rs2233678polymorphisminpin1promoterregionreducedcancerriskametaanalysis
AT gaoyong rs2233678polymorphisminpin1promoterregionreducedcancerriskametaanalysis