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Tumor evolutionary trajectories during the acquisition of invasiveness in early stage lung adenocarcinoma

Medicine and Health

Tumor evolutionary trajectories during the acquisition of invasiveness in early stage lung adenocarcinoma

S. Wang, M. Du, et al.

This study unveils intriguing evolutionary trajectories in early lung adenocarcinoma (LUAD), identifying distinct variant patterns in pre-invasive and invasive components. The research reveals how EGFR mutations may decrease post-invasiveness, possibly linked to B cell infiltration. Discover the insights from this pioneering research conducted by Siwei Wang and colleagues.

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~3 min • Beginner • English
Abstract
The evolutionary trajectories of early lung adenocarcinoma (LUAD) have not been fully elucidated. We hypothesize that genomic analysis between pre-invasive and invasive components will facilitate the description of LUAD evolutionary patterns. We micro-dissected malignant pulmonary nodules (MPNs) into paired pre-invasive and invasive components for panel-genome sequencing and recognize three evolutionary trajectories. Evolutionary mode 1 (EM1) demonstrates none of the common driver events between paired components, but rather two modes, EM2 and EM3, exhibit private variants restricted to pre-invasive and invasive components, respectively. When ancestral clones harbor EGFR mutations, truncal abundance significantly decrease after the acquisition of invasiveness, which may be associated with the intracellular accumulation of infiltrated B cells. Harboring EGFR mutations is critical to the selective pressure and further impacts the prognosis. Our findings extend the understanding of evolutionary trajectories during invasiveness acquisition in early LUAD.
Publisher
Nature Communications
Published On
Nov 27, 2020
Authors
Siwei Wang, Mulong Du, Jingyuan Zhang, Weizhang Xu, Qianyu Yuan, Ming Li, Jie Wang, Hongyu Zhu, Yuzhou Wang, Cheng Wang, Yuhua Gong, Xiaonan Wang, Zhibin Hu, David C. Christiani, Lin Xu, Hongbing Shen, Rong Yin
Tags
lung adenocarcinoma
evolutionary trajectories
EGFR mutations
invasiveness
B cell infiltration
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