Department of Thoracic Surgery, Jiangsu Key Laboratory of Molecular and Translational Cancer Research, Nanjing Medical University Affiliated Cancer Hospital & Jiangsu Cancer Hospital & Jiangsu Institute of Cancer Research, 21009, Nanjing, P.R. China.
Department of Biostatistics, Center for Global Health, School of Public Health, Nanjing Medical University, 211116, Nanjing, P.R. China.
Nat Commun. 2020 Nov 27;11(1):6083. doi: 10.1038/s41467-020-19855-x.
The evolutionary trajectories of early lung adenocarcinoma (LUAD) have not been fully elucidated. We hypothesize that genomic analysis between pre-invasive and invasive components will facilitate the description of LUAD evolutionary patterns. We micro-dissect malignant pulmonary nodules (MPNs) into paired pre-invasive and invasive components for panel-genomic sequencing and recognize three evolutionary trajectories. Evolutionary mode 1 (EM1) demonstrates none of the common driver events between paired components, but another two modes, EM2A and EM2B, exhibit critical private alterations restricted to pre-invasive and invasive components, respectively. When ancestral clones harbor EGFR mutations, truncal mutation abundance significantly decrease after the acquisition of invasiveness, which may be associated with the intratumoral accumulation of infiltrated B cells. Harboring EGFR mutations is critical to the selective pressure and further impacts the prognosis. Our findings extend the understanding of evolutionary trajectories during invasiveness acquisition in early LUAD.
早期肺腺癌 (LUAD) 的进化轨迹尚未完全阐明。我们假设,对侵袭前和侵袭成分之间的基因组分析将有助于描述 LUAD 的进化模式。我们将恶性肺结节 (MPN) 微解剖为配对的侵袭前和侵袭成分,进行面板基因组测序,并识别出三种进化轨迹。进化模式 1 (EM1) 在配对成分之间没有发现任何常见的驱动事件,但另外两种模式 EM2A 和 EM2B 分别表现出仅局限于侵袭前和侵袭成分的关键私有改变。当祖细胞携带 EGFR 突变时,在获得侵袭性后,主干突变丰度显著降低,这可能与浸润 B 细胞在肿瘤内的积累有关。携带 EGFR 突变对选择压力至关重要,并进一步影响预后。我们的研究结果扩展了对早期 LUAD 侵袭过程中进化轨迹的认识。