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昼夜节律基因多态性、夜班工作与前列腺癌风险:EPICAP 研究的结果。

Circadian genes polymorphisms, night work and prostate cancer risk: Findings from the EPICAP study.

机构信息

Université Paris-Saclay, UVSQ, Inserm, CESP, Villejuif, France.

Registre des Tumeurs de l'Hérault, EA 2415, ICM, Montpellier, France.

出版信息

Int J Cancer. 2020 Dec 1;147(11):3119-3129. doi: 10.1002/ijc.33139. Epub 2020 Jul 20.

DOI:10.1002/ijc.33139
PMID:32506468
Abstract

Over the past two decades, several studies have attempted to understand the hypothesis that disrupting the circadian rhythm may promote the development of cancer. Some have suggested that night work and some circadian genes polymorphisms are associated with cancer, including prostate cancer. Our study aims to test the hypothesis that prostate cancer risk among night workers may be modulated by genetic polymorphisms in the circadian pathway genes based on data from the EPICAP study, a population-based case-control study including 1511 men (732 cases/779 controls) with genotyped data. We estimated odds ratio (ORs) and P values of the association between prostate cancer and circadian gene variants using logistic regression models. We tested the interaction between circadian genes variants and night work indicators that were significantly associated with prostate cancer at pathway, gene and SNP levels. Analyses were also stratified by each of these night work indicators and by cancer aggressiveness. The circadian pathway was significantly associated with aggressive prostate cancer among night workers (P = .004), particularly for men who worked at night for <20 years (P = .0002) and those who performed long night shift (>10 hours, P = .001). At the gene level, we observed among night workers significant associations between aggressive prostate cancer and ARNTL, NPAS2 and RORA. At the SNP-level, no significant association was observed. Our findings provide some clues of a potential modulating effect of circadian genes in the relationship between night work and prostate cancer. Further investigation is warranted to confirm these findings and to better elucidate the biological pathways involved.

摘要

在过去的二十年中,有几项研究试图理解这样一种假设,即扰乱生物钟可能会促进癌症的发展。一些研究表明,夜班工作和一些生物钟基因多态性与癌症有关,包括前列腺癌。我们的研究旨在根据 EPICAP 研究的数据测试这样一种假设,即夜班工作者的前列腺癌风险可能受到生物钟途径基因遗传多态性的调节,该研究是一项基于人群的病例对照研究,包括 1511 名男性(732 例/779 例对照),这些男性有基因分型数据。我们使用逻辑回归模型估计了前列腺癌与生物钟基因变异之间的关联的比值比(OR)和 P 值。我们测试了生物钟基因变异与在途径、基因和 SNP 水平与前列腺癌显著相关的夜班工作指标之间的相互作用。还按这些夜班工作指标和癌症侵袭性对分析进行分层。在夜班工作者中,生物钟途径与侵袭性前列腺癌显著相关(P =.004),特别是对于夜间工作<20 年的男性(P =.0002)和夜间工作时间较长的男性(>10 小时,P =.001)。在基因水平上,我们观察到在夜班工作者中,侵袭性前列腺癌与 ARNTL、NPAS2 和 RORA 之间存在显著关联。在 SNP 水平上,没有观察到显著关联。我们的研究结果为生物钟基因在夜班工作与前列腺癌之间的关系中可能存在的调节作用提供了一些线索。需要进一步的调查来证实这些发现,并更好地阐明所涉及的生物学途径。

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