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整合基因组分析揭示了 PLCO 队列中与肺癌风险相关的延长种系纯合性。

Integrative genomic analysis reveals extended germline homozygosity with lung cancer risk in the PLCO cohort.

机构信息

Genomic Medicine Institute, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio, United States of America.

出版信息

PLoS One. 2012;7(2):e31975. doi: 10.1371/journal.pone.0031975. Epub 2012 Feb 27.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8b3/3288062/531df44e2303/pone.0031975.g001.jpg

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