Genomic Medicine Institute, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio, United States of America.
PLoS One. 2012;7(2):e31975. doi: 10.1371/journal.pone.0031975. Epub 2012 Feb 27.
Susceptibility to common cancers is multigenic resulting from low-to-high penetrance predisposition-factors and environmental exposure. Genomic studies suggest germline homozygosity as a novel low-penetrance factor contributing to common cancers. We hypothesized that long homozygous regions (tracts-of-homozygosity [TOH]) harbor tobacco-dependent and independent lung-cancer predisposition (or protection) genes. We performed in silico genome-wide SNP-array-based analysis of lung-cancer patients of European-ancestry from the PLCO screening-trial cohort to identify TOH regions amongst 788 cancer-cases and 830 ancestry-matched controls. Association analyses was then performed between presence of lung cancer and common(c)TOHs (operationally defined as 10 or more subjects sharing ≥100 identical homozygous calls), aTOHs (allelically-matched groups within a cTOH), demographics and tobacco-exposure. Finally, integration of significant c/aTOH with transcriptome was performed to functionally-map lung-cancer risk-genes. After controlling for demographics and smoking, we identified 7 cTOHs and 5 aTOHs associated with lung cancer (adjusted p<0.01). Three cTOHs were over-represented in cases over controls (OR = 1.75-2.06, p = 0.007-0.001), whereas 4 were under-represented (OR = 0.28-0.69, p = 0.006-0.001). Interaction between smoking status and cTOH3/aTOH2 (2p16.3-2p16.1) was observed (adjusted p<0.03). The remaining significant aTOHs have ORs 0.23-0.50 (p = 0.004-0.006) and 2.95-3.97 (p = 0.008-0.001). After integrating significant cTOH/aTOHs with publicly-available lung-cancer transcriptome datasets followed by filtering based on lung cancer and its relevant pathways revealed 9 putative predisposing genes (p<0.0001). In conclusion, differentially-distributed cTOH/aTOH genomic variants between cases and controls harbor sets of plausible differentially-expressed genes accounting for the complexity of lung-cancer predisposition.
常见癌症的易感性是多基因的,由低到高外显率的易感因素和环境暴露引起。基因组研究表明,种系纯合性是导致常见癌症的一种新的低外显率因素。我们假设长纯合区域(同质性区域[TOH])是烟草依赖和独立的肺癌易感性(或保护)基因的所在地。我们对来自 PLCO 筛查试验队列的欧洲血统肺癌患者进行了基于全基因组 SNP 芯片的计算机分析,以确定 788 例癌症病例和 830 例匹配的对照组中 TOH 区域。然后,在存在肺癌的情况下,对常见(c)TOH(操作定义为 10 个或更多个体共享≥100 个相同的纯合性调用)、aTOH(cTOH 内等位基因匹配的组)、人口统计学和烟草暴露之间进行关联分析。最后,对显著的 c/aTOH 与转录组进行整合,以功能映射肺癌风险基因。在控制人口统计学和吸烟因素后,我们鉴定出与肺癌相关的 7 个 cTOH 和 5 个 aTOH(调整后的 p<0.01)。三个 cTOH 在病例中比对照中更为常见(OR=1.75-2.06,p=0.007-0.001),而 4 个则较少见(OR=0.28-0.69,p=0.006-0.001)。观察到吸烟状况与 cTOH3/aTOH2(2p16.3-2p16.1)之间的相互作用(调整后的 p<0.03)。其余显著的 aTOH 的 OR 为 0.23-0.50(p=0.004-0.006)和 2.95-3.97(p=0.008-0.001)。将显著的 cTOH/aTOH 与公开的肺癌转录组数据集进行整合,然后根据肺癌及其相关途径进行过滤,揭示了 9 个可能的易感基因(p<0.0001)。总之,病例和对照组之间差异分布的 cTOH/aTOH 基因组变异携带有一系列可能的差异表达基因,解释了肺癌易感性的复杂性。