Nongenetic Evolution Drives Lung Adenocarcinoma Spatial Heterogeneity and Progression

生物 腺癌 表观遗传学 肺癌 背景(考古学) 遗传异质性 癌症的体细胞进化 肿瘤进展 癌症 病理 肿瘤异质性 表型 癌症研究 医学 遗传学 基因 古生物学
作者
Daniele Tavernari,Elena Battistello,Elie Dheilly,Aaron S. Petruzzella,Marco Mina,Jessica Sordet‐Dessimoz,Solange Peters,Thorsten Krueger,David Gfeller,Nicolò Riggi,Elisa Oricchio,Igor Letovanec,Giovanni Ciriello
出处
期刊:Cancer Discovery [American Association for Cancer Research]
卷期号:11 (6): 1490-1507 被引量:89
标识
DOI:10.1158/2159-8290.cd-20-1274
摘要

Cancer evolution determines molecular and morphologic intratumor heterogeneity and challenges the design of effective treatments. In lung adenocarcinoma, disease progression and prognosis are associated with the appearance of morphologically diverse tumor regions, termed histologic patterns. However, the link between molecular and histologic features remains elusive. Here, we generated multiomics and spatially resolved molecular profiles of histologic patterns from primary lung adenocarcinoma, which we integrated with molecular data from >2,000 patients. The transition from indolent to aggressive patterns was not driven by genetic alterations but by epigenetic and transcriptional reprogramming reshaping cancer cell identity. A signature quantifying this transition was an independent predictor of patient prognosis in multiple human cohorts. Within individual tumors, highly multiplexed protein spatial profiling revealed coexistence of immune desert, inflamed, and excluded regions, which matched histologic pattern composition. Our results provide a detailed molecular map of lung adenocarcinoma intratumor spatial heterogeneity, tracing nongenetic routes of cancer evolution. SIGNIFICANCE: Lung adenocarcinomas are classified based on histologic pattern prevalence. However, individual tumors exhibit multiple patterns with unknown molecular features. We characterized nongenetic mechanisms underlying intratumor patterns and molecular markers predicting patient prognosis. Intratumor patterns determined diverse immune microenvironments, warranting their study in the context of current immunotherapies.This article is highlighted in the In This Issue feature, p. 1307.
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