Genomic and immune profiling of pre-invasive lung adenocarcinoma

Author:

Chen Haiquan,Carrot-Zhang JianORCID,Zhao Yue,Hu Haichuan,Freeman Samuel S.,Yu Su,Ha GavinORCID,Taylor Alison M.,Berger Ashton C.,Westlake Lindsay,Zheng Yuanting,Zhang Jiyang,Ramachandran Aruna,Zheng Qiang,Pan Yunjian,Zheng Difan,Zheng Shanbo,Cheng Chao,Kuang Muyu,Zhou Xiaoyan,Zhang Yang,Li Hang,Ye Ting,Ma Yuan,Gao Zhendong,Tao Xiaoting,Han Han,Shang JunORCID,Yu Ying,Bao Ding,Huang Yechao,Li Xiangnan,Zhang Yawei,Xiang Jiaqing,Sun Yihua,Li Yuan,Cherniack Andrew D.ORCID,Campbell Joshua D.,Shi Leming,Meyerson MatthewORCID

Abstract

AbstractAdenocarcinoma in situ and minimally invasive adenocarcinoma are the pre-invasive forms of lung adenocarcinoma. The genomic and immune profiles of these lesions are poorly understood. Here we report exome and transcriptome sequencing of 98 lung adenocarcinoma precursor lesions and 99 invasive adenocarcinomas. We have identified EGFR, RBM10, BRAF, ERBB2, TP53, KRAS, MAP2K1 and MET as significantly mutated genes in the pre/minimally invasive group. Classes of genome alterations that increase in frequency during the progression to malignancy are revealed. These include mutations in TP53, arm-level copy number alterations, and HLA loss of heterozygosity. Immune infiltration is correlated with copy number alterations of chromosome arm 6p, suggesting a link between arm-level events and the tumor immune environment.

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry

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