Tracing Oncogene Rearrangements in the Mutational History of Lung Adenocarcinoma.
Cell
; 177(7): 1842-1857.e21, 2019 06 13.
Article
en En
| MEDLINE
| ID: mdl-31155235
ABSTRACT
Mutational processes giving rise to lung adenocarcinomas (LADCs) in non-smokers remain elusive. We analyzed 138 LADC whole genomes, including 83 cases with minimal contribution of smoking-associated mutational signature. Genomic rearrangements were not correlated with smoking-associated mutations and frequently served as driver events of smoking-signature-low LADCs. Complex genomic rearrangements, including chromothripsis and chromoplexy, generated 74% of known fusion oncogenes, including EML4-ALK, CD74-ROS1, and KIF5B-RET. Unlike other collateral rearrangements, these fusion-oncogene-associated rearrangements were frequently copy-number-balanced, representing a genomic signature of early oncogenesis. Analysis of mutation timing revealed that fusions and point mutations of canonical oncogenes were often acquired in the early decades of life. During a long latency, cancer-related genes were disrupted or amplified by complex rearrangements. The genomic landscape was different between subgroups-EGFR-mutant LADCs had frequent whole-genome duplications with p53 mutations, whereas fusion-oncogene-driven LADCs had frequent SETD2 mutations. Our study highlights LADC oncogenesis driven by endogenous mutational processes.
Palabras clave
Texto completo:
1
Colección:
01-internacional
Banco de datos:
MEDLINE
Asunto principal:
Reordenamiento Génico
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Proteínas de Fusión Oncogénica
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Adenocarcinoma del Pulmón
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Neoplasias Pulmonares
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Mutación
Límite:
Female
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Humans
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Male
Idioma:
En
Revista:
Cell
Año:
2019
Tipo del documento:
Article