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High-depth high-accuracy microsatellite genotyping enables precision lung cancer risk classification

机译:高深度高精度微卫星基因分型可实现精确的肺癌风险分类

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摘要

There remains a large discrepancy between the known genetic contributions to cancer and that which can be explained by genomic variants, both inherited and somatic. Recently, understudied repetitive DNA regions called microsatellites have been identified as genetic risk markers for a number of diseases including various cancers (breast, ovarian and brain). In this study, we demonstrate an integrated process for identifying and further evaluating microsatellite-based risk markers for lung cancer using data from the cancer genome atlas and the 1000 genomes project. Comparing whole-exome germline sequencing data from 488 TCGA lung cancer samples to germline exome data from 390 control samples from the 1000 genomes project, we identified 119 potentially informative microsatellite loci. These loci were found to be able to distinguish between cancer and control samples with sensitivity and specificity ratios over 0.8. Then these loci, supplemented with additional loci from other cancers and controls, were evaluated using a target enrichment kit and sample-multiplexed nextgen sequencing. Thirteen of the 119 risk markers were found to be informative in a well powered study (>0.99 for a 0.95 confidence interval) using high-depth (579x±315) nextgen sequencing of 30 lung cancer and 89 control samples, resulting in sensitivity and specificity ratios of 0.90 and 0.94, respectively. When 8 loci harvested from the bioinformatic analysis of other cancers are added to the classifier, then the sensitivity and specificity rise to 0.93 and 0.97, respectively. Analysis of the genes harboring these loci revealed two genes (ARID1B and REL) and two significantly enriched pathways (chromatin organization and cellular stress response) suggesting that the process of lung carcinogenesis is linked to chromatin remodeling, inflammation, and tumor microenvironment restructuring. We illustrate that high-depth sequencing enables a high-precision microsatellite-based risk classifier analysis approach. This microsatellite-based platform confirms the potential to create clinically actionable diagnostics for lung cancer.
机译:已知的对癌症的遗传贡献与可以由遗传和体细胞的基因组变异解释的差异很大。最近,人们已经研究了被研究不足的称为微卫星的重复DNA区域,作为许多疾病的遗传风险标记,包括各种癌症(乳腺癌,卵巢癌和脑癌)。在这项研究中,我们展示了使用癌症基因组图谱和1000个基因组计划中的数据鉴定和进一步评估基于微卫星的肺癌危险标志物的集成过程。将来自488个TCGA肺癌样本的全基因组种系测序数据与来自1000个基因组计划的390个对照样品的种系外显子组数据进行比较,我们确定了119个可能提供信息的微卫星基因座。发现这些基因座能够区分灵敏度和特异性比超过0.8的癌症样品与对照样品。然后,使用靶标富集试剂盒和样品多重nextgen测序评估这些基因座,并补充其他癌症和对照的其他基因座。在一项功能强大的研究(> 0.99,对于0.95置信区间)中,使用高深度(579x±315)nextgen测序技术对30个肺癌和89个对照样品进行了测序,发现119个风险标记中的13个具有参考价值。比分别为0.90和0.94。当从其他癌症的生物信息学分析中收获的8个基因座被添加到分类器时,灵敏度和特异性分别上升到0.93和0.97。对具有这些基因座的基因的分析揭示了两个基因(ARID1B和REL)和两个显着富集的途径(染色质组织和细胞应激反应),表明肺癌的形成过程与染色质重塑,炎症和肿瘤微环境重塑有关。我们说明了深度测序可实现基于微卫星的高精度风险分类器分析方法。这个基于微卫星的平台证实了创建针对肺癌的临床可行诊断方法的潜力。

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