Department of Epidemiology, University of Washington, Seattle, Washington.
Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Cancer Epidemiol Biomarkers Prev. 2020 Sep;29(9):1817-1824. doi: 10.1158/1055-9965.EPI-19-1507. Epub 2020 Jun 25.
Telomeres play an important role in colorectal cancer prognosis. Variation in telomere maintenance genes may be associated with survival after colorectal cancer diagnosis, but evidence is limited. In addition, possible interactions between telomere maintenance genes and prognostic factors, such as smoking and sex, also remain to be investigated.
We conducted gene-wide analyses of colorectal cancer prognosis in 4,896 invasive colorectal cancer cases from the Genetics and Epidemiology of Colorectal Cancer Consortium (GECCO); 1,871 common variants within 13 telomere maintenance genes were included. Cox models were fit to estimate associations of these variants individually with overall and colorectal cancer-specific survival. Likelihood ratio tests were used to test for interaction by smoking and sex. values were adjusted using Bonferroni correction.
The association between minor allele of rs7200950 () with colorectal cancer-specific survival varied significantly by smoking pack-years (corrected = 0.049), but no significant trend was observed. By sex, minor alleles for rs2975843 (), rs75676021 (), and rs74429678 () were associated with decreased overall and/or colorectal cancer-specific survival in women but not in men.
Our study reported a gene-wide statistically significant interaction with sex (). Although significant interaction by smoking pack-years () was observed, there was no evidence of a dose response. Validation of these findings in other large studies and further functional annotation on these SNPs are warranted.
Our study found a gene-smoking and gene-sex interaction on survival after colorectal cancer diagnosis, providing new insights into the role of genetic polymorphisms in telomere maintenance on colorectal cancer prognosis.
端粒在结直肠癌预后中起着重要作用。端粒维持基因的变异可能与结直肠癌诊断后的生存有关,但证据有限。此外,端粒维持基因与预后因素(如吸烟和性别)之间的可能相互作用仍有待研究。
我们对遗传与流行病学结直肠癌协作组(GECCO)的 4896 例侵袭性结直肠癌病例进行了全基因组分析;纳入了 13 个端粒维持基因中的 1871 个常见变异。使用 Cox 模型分别估计这些变体与总体和结直肠癌特异性生存的关联。使用似然比检验来检验吸烟和性别之间的交互作用。使用 Bonferroni 校正调整 值。
rs7200950 ()的次要等位基因与结直肠癌特异性生存的关联在吸烟包年数方面存在显著差异(校正 = 0.049),但未观察到明显趋势。按性别,rs2975843 ()、rs75676021 ()和 rs74429678 ()的次要等位基因与女性的总体和/或结直肠癌特异性生存降低相关,但与男性无关。
我们的研究报告了与性别()存在全基因组统计学显著的交互作用。虽然观察到与吸烟包年数()存在显著的交互作用,但没有证据表明存在剂量反应。需要在其他大型研究中验证这些发现,并进一步对这些 SNP 进行功能注释。
我们的研究发现了与生存相关的基因-吸烟和基因-性别相互作用,为遗传多态性在端粒维持对结直肠癌预后中的作用提供了新的见解。