Single Nucleotide Polymorphisms of PIN1 Promoter Region and Cancer Risk: Evidence from a Meta-Analysis

被引:8
作者
Peng, Jing-Jing [1 ]
Wei, Dong [1 ]
Li, Dong [1 ]
Fu, Zeng-Qiang [1 ]
Tan, Yong [1 ]
Xu, Tao [1 ]
Zhou, Jing-Jun [1 ]
Zhang, Tao [1 ]
机构
[1] Gen Hosp Chengdu Mil Dist, Dept Oncol, Chengdu, Sichuan, Peoples R China
来源
PLOS ONE | 2013年 / 8卷 / 08期
关键词
PROLYL ISOMERASE PIN1; SQUAMOUS-CELL CARCINOMA; BREAST-CANCER; DECREASED RISK; LUNG-CANCER; GENE; -842G-GREATER-THAN-C; SUSCEPTIBILITY; ISOMERIZATION; VARIANTS;
D O I
10.1371/journal.pone.0070990
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Peptidylprolyl cis/trans isomerase NIMA-interacting 1 (PIN1) is involved in the process of tumorigenesis. The two single nucleotide polymorphisms (-677T>C, -842G>C) in the PIN1 promoter region have been suspected of being associated with cancer risk for years, but the conclusion is still inconclusive. Methods: Eligible case-control studies were retrieved by searching databases and references of related reviews and studies. Genotype distribution data, adjusted odds ratios (ORs) and 95% confidence (CIs) intervals were extracted to calculate pooled ORs. Results: A total of 4619 cancer cases and 4661 controls were included in this meta-analysis. Overall, the PIN1 -667T>C polymorphism was not associated with cancer risk, while the -842C allele was significantly associated with reduced cancer risk (CC+GC vs. GG, OR = 0.725, 95% CI: 0.607-0.865; P-heterogeneity = 0.012 and GC vs. GG: OR = 0.721, 95% CI: 0.591-0.880; P-heterogeneity = 0.003). Results from genotype distribution data were in agreement with those calculated with adjusted ORs and 95% CIs. No publication bias was detected. Conclusions: Results of this meta-analysis suggest that the PIN1 -842G>C polymorphism is associated with decreased cancer risk, but that the -667T>C polymorphism is not.
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页数:9
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