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从不吸烟者肺癌预后的遗传决定因素:国际肺癌联盟的 pooled 分析。

Genetic Determinants of Lung Cancer Prognosis in Never Smokers: A Pooled Analysis in the International Lung Cancer Consortium.

机构信息

Prosserman Centre for Population Health Research, Lunenfeld-Tanenbaum Research Institute, Sinai Health System, Toronto, Canada.

Mayo Clinic, Scottsdale, Arizona.

出版信息

Cancer Epidemiol Biomarkers Prev. 2020 Oct;29(10):1983-1992. doi: 10.1158/1055-9965.EPI-20-0248. Epub 2020 Jul 22.

Abstract

BACKGROUND

Lung cancer remains the leading cause of cancer death worldwide, with 15% to 20% occurring in never smokers. To assess genetic determinants for prognosis among never smokers, we conducted a genome-wide investigation in the International Lung Cancer Consortium (ILCCO).

METHODS

Genomic and clinical data from 1,569 never-smoking patients with lung cancer of European ancestry from 10 ILCCO studies were included. HRs and 95% confidence intervals of overall survival were estimated. We assessed whether the associations were mediated through mRNA expression-based 1,553 normal lung tissues from the lung expression quantitative trait loci (eQTL) dataset and Genotype-Tissue Expression (GTEx). For cross-ethnicity generalization, we assessed the associations in a Japanese study ( = 887).

RESULTS

One locus at 13q22.2 was associated with lung adenocarcinoma survival at genome-wide level, with carriers of rs12875562-T allele exhibiting poor prognosis [HR = 1.71 (1.41-2.07), = 3.60 × 10], and altered mRNA expression of in lung tissue (GTEx, = 9.40 × 10; Lung eQTL dataset, = 0.003). Furthermore, 2 of 11 independent loci that reached the suggestive significance level ( < 10) were significant eQTL affecting mRNA expression of nearby genes in lung tissues, including at 1p36.13 and at 9q34.3. One locus encoding at 4p14 showed associations in both European [HR = 0.50 (0.38-0.66), = 6.92 × 10] and Japanese populations [HR = 0.79 (0.67-0.94), = 0.007].

CONCLUSIONS

Based on the largest genomic investigation on the lung cancer prognosis of never smokers to date, we observed that lung cancer prognosis is affected by inherited genetic variants.

IMPACT

We identified one locus near at genome-wide level and several potential prognostic genes with -effect on mRNA expression. Further functional genomics work is required to understand their role in tumor progression.

摘要

背景

肺癌仍然是全世界癌症死亡的主要原因,其中 15%至 20%发生在从不吸烟的人群中。为了评估从不吸烟的肺癌患者的遗传预后决定因素,我们在国际肺癌协作组(ILCCO)中进行了全基因组研究。

方法

纳入了来自 10 项 ILCCO 研究的 1569 名欧洲血统的从不吸烟的肺癌患者的基因组和临床数据。使用 HR 和 95%置信区间来估计总生存期。我们评估了这些关联是否通过基于 mRNA 表达的 1553 个正常肺组织的肺表达定量性状(eQTL)数据集和基因型组织表达(GTEx)来介导。为了进行跨种族概括,我们评估了日本研究中的关联(n=887)。

结果

在全基因组水平上,13q22.2 上的一个位点与肺腺癌的生存相关,携带 rs12875562-T 等位基因的患者预后较差[HR=1.71(1.41-2.07),P=3.60×10],并且肺组织中 的 mRNA 表达发生改变(GTEx,P=9.40×10;Lung eQTL 数据集,P=0.003)。此外,在达到提示性显著水平(P<10)的 11 个独立位点中,有 2 个是影响肺组织中附近基因 mRNA 表达的独立 eQTL,包括 1p36.13 上的 位点和 9q34.3 上的 位点。位于 4p14 上的一个编码 位点与欧洲人群(HR=0.50(0.38-0.66),P=6.92×10)和日本人群(HR=0.79(0.67-0.94),P=0.007)均相关。

结论

基于迄今为止针对从不吸烟的肺癌患者预后的最大基因组研究,我们观察到肺癌预后受到遗传变异的影响。

意义

我们在全基因组水平上确定了一个位于 附近的位点和几个具有 -效应的潜在预后基因,这些基因影响 mRNA 表达。需要进一步进行功能基因组学研究以了解它们在肿瘤进展中的作用。

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