National Cancer Center Graduate School of Cancer Science and Policy, Goyang-si, 10408, Republic of Korea.
Hospital, National Cancer Center, Goyang-si, 10408, Republic of Korea.
Sci Rep. 2019 Jul 29;9(1):10982. doi: 10.1038/s41598-019-47480-2.
Our purpose is to investigate the impact of circadian and melatonin pathway genes as well as their interactions with night-shift work (NSW) on breast cancer risk in Korean women. Information about NSW and other covariates was collected using a structured questionnaire and twenty-two polymorphisms in 11 genes were analyzed in a hospital-based case-control study with 941 cases of breast cancer and 959 controls. In analysis of the main effects of each single nucleotide polymorphisms(SNPs), variants in CLOCK rs11133373 was associated with breast cancer risk even after false discovery rate (FDR) correction (Odd Ratios (OR) = 1.38 (95% Confident Interval (CI) 1.14-1.69) in CG and CC compared to GG genotype. Analysis of MTNR1A rs2119882 demonstrated a decreased risk of breast cancer in CC compared to TT (p-FDR = 0.043). A correlation between NSW and breast cancer interaction was found in two loci. NSW increased risk of breast cancer in women who carried the heterozygote genotype of CRY2 rs2292912 (OR = 1.98, 95% CI = 1.14-3.44) or carried at least one minor allele of RORA rs1482057 (OR = 2.20, 95% CI = 1.10-4.37). Our study results support a putative role for several loci of circadian genes and genes of melatonin biosynthesis and their interaction, and the gene interactions with NSW in the development of breast cancer.
我们的目的是探讨生物钟和褪黑素通路基因及其与夜班工作(NSW)的相互作用对韩国女性乳腺癌风险的影响。使用结构化问卷收集有关 NSW 和其他协变量的信息,并在一项基于医院的病例对照研究中分析了 11 个基因中的 22 个多态性,该研究纳入了 941 例乳腺癌病例和 959 例对照。在分析每个单核苷酸多态性(SNP)的主要效应时,即使在经过错误发现率(FDR)校正后,CLOCK rs11133373 的变体与乳腺癌风险相关(CG 和 CC 基因型与 GG 基因型相比,比值比(OR)为 1.38(95%置信区间(CI)为 1.14-1.69)。MTNR1A rs2119882 的分析表明,与 TT 相比,CC 型乳腺癌发病风险降低(p-FDR=0.043)。在两个位点发现了 NSW 和乳腺癌相互作用的相关性。在携带 CRY2 rs2292912 杂合基因型(OR=1.98,95%CI=1.14-3.44)或至少携带一个 RORA rs1482057 次要等位基因的女性中,NSW 增加了乳腺癌的发病风险(OR=2.20,95%CI=1.10-4.37)。我们的研究结果支持几个生物钟基因和褪黑素生物合成基因及其与 NSW 的相互作用以及基因相互作用在乳腺癌发生中的潜在作用。