Geng Peiliang, Ou Juanjuan, Li Jianjun, Wang Ning, Xie Ganfeng, Sa Rina, Liu Chen, Xiang Lisha, Liang Houjie
From the Department of Oncology and Southwest Cancer Center, Southwest Hospital, Third Military Medical University, Chongqing, China.
Medicine (Baltimore). 2015 Apr;94(13):e568. doi: 10.1097/MD.0000000000000568.
The genes along the circadian pathways control and modulate circadian rhythms essential for the maintenance of physiological homeostasis through self-sustained transcription-translation feedback loops. PER3 (period 3) is a circadian pathway gene and its variants (rs1012477, 4/5-repeat) have frequently been associated with human cancer. The mixed findings, however, make the role of the 2 variants in cancer susceptibility elusive. We aimed in this article to clarify the association of PER3 variants with cancer. We collected genetic data from 8 studies, providing 6149 individuals for rs1012477 and 5241 individuals for 4/5-repeat. Based on the genotype and allele frequency, we chose the fixed-effects model to estimate risk of cancer. Overall analysis did not suggest a global role of rs1012477 in cancer susceptibility. For PER3 4/5-repeat variant, we found a moderate increase in risk of cancer among individuals with the 5-allele compared to individuals with the 4-allele, although this association was not statistically significant (homozygous model: odds ratio [OR] 1.17, 95% confidence interval [CI] 0.81-1.67; recessive model: OR 1.17, 95% CI 0.82-1.67). No substantial heterogeneity was revealed in this analysis. Our meta-analysis provides no evidence supporting a global association of PER3 genetic variants with the incidence of cancer.
昼夜节律途径中的基因通过自我维持的转录-翻译反馈环来控制和调节维持生理稳态所必需的昼夜节律。PER3(周期蛋白3)是一种昼夜节律途径基因,其变体(rs1012477,4/5重复)经常与人类癌症相关。然而,这些混合的研究结果使得这两种变体在癌症易感性中的作用难以捉摸。我们在本文中的目的是阐明PER3变体与癌症的关联。我们从8项研究中收集了遗传数据,其中rs1012477有6149名个体,4/5重复有5241名个体。基于基因型和等位基因频率,我们选择固定效应模型来估计癌症风险。总体分析并未表明rs1012477在癌症易感性中具有全局性作用。对于PER3 4/5重复变体,我们发现与具有4等位基因的个体相比,具有5等位基因的个体患癌风险有适度增加,尽管这种关联在统计学上并不显著(纯合子模型:比值比[OR]为1.17,95%置信区间[CI]为0.81 - 1.67;隐性模型:OR为1.17,95% CI为0.82 - 1.67)。该分析未发现实质性异质性。我们的荟萃分析没有提供证据支持PER3基因变体与癌症发病率之间存在全局性关联。