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Bridging the clinical gaps: genetic epigenetic and transcriptomic biomarkers for the early detection of lung cancer in the post-National Lung Screening Trial era

机译:弥合临床空白:在国家肺癌筛查试验后的早期检测肺癌的遗传表观遗传和转录组生物标志物

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摘要

Lung cancer is the leading cause of cancer death worldwide in part due to our inability to identify which smokers are at highest risk and the lack of effective tools to detect the disease at its earliest and potentially curable stage. Recent results from the National Lung Screening Trial have shown that annual screening of high-risk smokers with low-dose helical computed tomography of the chest can reduce lung cancer mortality. However, molecular biomarkers are needed to identify which current and former smokers would benefit most from annual computed tomography scan screening in order to reduce the costs and morbidity associated with this procedure. Additionally, there is an urgent clinical need to develop biomarkers that can distinguish benign from malignant lesions found on computed tomography of the chest given its very high false positive rate. This review highlights recent genetic, transcriptomic and epigenomic biomarkers that are emerging as tools for the early detection of lung cancer both in the diagnostic and screening setting.
机译:肺癌是全球癌症死亡的主要原因,部分原因是我们无法确定哪些吸烟者处于最高风险,并且缺乏有效的工具来尽早发现并可能治愈该疾病。全国肺部筛查试验的最新结果表明,每年对胸部低剂量螺旋计算机断层扫描的高危吸烟者进行筛查可以降低肺癌的死亡率。但是,需要分子生物标记物来确定哪些吸烟者和过去的吸烟者将从年度计算机断层扫描扫描筛查中受益最大,以便降低与此过程相关的成本和发病率。另外,迫切需要开发一种生物标记物,以区分出良性和恶性病灶,因为它们的假阳性率非常高,因此可以在胸部计算机体层摄影术中发现良性和恶性病变。这篇综述重点介绍了最近的遗传,转录组和表观基因组生物标志物,这些标志物已成为在诊断和筛查背景下早期检测肺癌的工具。

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