Department of Oncology, the General Hospital of Chengdu Military District, Chengdu, Sichuan, P.R. China.
PLoS One. 2013 Aug 16;8(8):e70990. doi: 10.1371/journal.pone.0070990. eCollection 2013.
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.
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.
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.
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.
肽基脯氨酰顺/反异构酶 NIMA 相互作用蛋白 1(PIN1)参与肿瘤发生过程。PIN1 启动子区域的两个单核苷酸多态性(-677T>C、-842G>C)多年来一直被怀疑与癌症风险相关,但结论仍不确定。
通过搜索数据库和相关综述及研究的参考文献,检索出符合条件的病例对照研究。提取基因型分布数据、调整后的比值比(OR)和 95%置信区间(CI),以计算汇总 OR。
本荟萃分析共纳入 4619 例癌症病例和 4661 例对照。总体而言,PIN1-667T>C 多态性与癌症风险无关,而-842C 等位基因与降低癌症风险显著相关(CC+GC 与 GG,OR=0.725,95%CI:0.607-0.865;P(异质性)=0.012 和 GC 与 GG:OR=0.721,95%CI:0.591-0.880;P(异质性)=0.003)。基因型分布数据的结果与调整后的 OR 和 95%CI 计算的结果一致。未发现发表偏倚。
本荟萃分析结果表明,PIN1-842G>C 多态性与降低癌症风险相关,但-667T>C 多态性则不然。