Multi-region exome sequencing reveals genomic evolution from preneoplasia to lung adenocarcinoma.

Research paper by Xin X Hu, Junya J Fujimoto, Lisha L Ying, Junya J Fukuoka, Kazuto K Ashizawa, Wenyong W Sun, Alexandre A Reuben, Chi-Wan CW Chow, Nicholas N McGranahan, Runzhe R Chen, Jinlin J Hu, Myrna C MC Godoy, Kazuhiro K Tabata, Kishio K Kuroda, Lei L Shi, et al.

Indexed on: 12 May '20Published on: 07 Jul '19Published in: Nature communications


There has been a dramatic increase in the detection of lung nodules, many of which are preneoplasia atypical adenomatous hyperplasia (AAH), adenocarcinoma in situ (AIS), minimally invasive adenocarcinoma (MIA) or invasive adenocarcinoma (ADC). The molecular landscape and the evolutionary trajectory of lung preneoplasia have not been well defined. Here, we perform multi-region exome sequencing of 116 resected lung nodules including AAH (n = 22), AIS (n = 27), MIA (n = 54) and synchronous ADC (n = 13). Comparing AAH to AIS, MIA and ADC, we observe progressive genomic evolution at the single nucleotide level and demarcated evolution at the chromosomal level supporting the early lung carcinogenesis model from AAH to AIS, MIA and ADC. Subclonal analyses reveal a higher proportion of clonal mutations in AIS/MIA/ADC than AAH suggesting neoplastic transformation of lung preneoplasia is predominantly associated with a selective sweep of unfit subclones. Analysis of multifocal pulmonary nodules from the same patients reveal evidence of convergent evolution.