Stepwise evolutionary genomics of early-stage lung adenocarcinoma manifesting as pure, heterogeneous and part-solid ground-glass nodules

腺癌 外显子组测序 癌症的体细胞进化 突变 生物 基因组学 阶段(地层学) 肺癌 癌症研究 遗传学 病理 癌症 基因组 基因 医学 内科学 古生物学
作者
Hao Li,Zewen Sun,Rongxin Xiao,Qingyi Qi,Xiao Li,Haiyan Huang,Xuan Wang,Jian Zhou,Zhenfan Wang,Ke Liu,Ping Yin,Fan Yang,Jun Wang
出处
期刊:British Journal of Cancer [Springer Nature]
卷期号:127 (4): 747-756 被引量:11
标识
DOI:10.1038/s41416-022-01821-7
摘要

BackgroundThis study was designed to unravel the genomic landscape and evolution of early-stage subsolid lung adenocarcinomas (SSN-LUADs) manifesting as pure ground-glass nodules (pGGNs), heterogeneous ground-glass nodules (HGGNs) and part-solid nodules (PSNs).MethodsSamples subjected to either broad-panel next-generation sequencing (NGS) or whole-exome sequencing (WES) were included. Clinicopathologic and genomic features were compared among pGGN, HGGN and PSN, while tumour evolutionary trajectories and mutational signatures were evaluated in the entire cohort.ResultsIn total, 247 SSN-LUAD samples subjected to broad-panel NGS and 125 to WES were identified. Compared with PSNs, HGGNs had significantly lower tumour mutation count (P < 0.001), genomic alteration count (P < 0.001), and intra-tumour heterogeneity (P = 0.005). Statistically significant upward trends were observed in alterations involving driver mutations and oncogenic pathways from pGGNs to HGGNs to PSNs. EGFR mutation was proved to be a key early event in the progression of SSN-LUADs, with subsequently two evolutionary trajectories involving either RBM10 or TP53 mutation in the cancer-evolution models.ConclusionsThis study provided evidence for unravelling the previously unknown genomic underpinnings associated with SSN-LUAD evolution from pGGN to HGGN to PSN, proving that HGGN was an intermediate SSN form between pGGN and PSN genetically.
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