生物
野战癌变
癌变
基础(医学)
细胞
病变
肺
基底细胞
癌症的体细胞进化
致癌物
病理
肺癌
运动性
电池类型
癌症研究
细胞生物学
遗传学
癌症
内科学
医学
内分泌学
胰岛素
作者
Sandra Gómez‐López,Ahmed Alhendi,Moritz J. Przybilla,Ignacio Bordeu,Zoe E. Whiteman,Timothy Butler,Maral J. Rouhani,Lukas Kalinke,Imran Uddin,Kate E. J. Davies,Deepak P. Chandrasekharan,Marta Lebrusant‐Fernandez,Abigail Y. L. Shurr,Pascal F. Durrenberger,David A. Moore,Mary Falzon,James L. Reading,Iñigo Martincorena,Benjamin D. Simons,Peter J. Campbell
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2025-05-01
标识
DOI:10.1126/science.ads9145
摘要
Preinvasive squamous lung lesions are precursors of lung squamous cell carcinoma (LUSC). The cellular events underlying lesion formation are unknown. Using a carcinogen-induced model of LUSC with no added genetic hits or cell type bias, we find that carcinogen exposure leads to non-neutral competition among basal cells, aberrant clonal expansions, and basal cell mobilization along the airways. Ultimately, preinvasive lesions develop from a few highly mutated clones that dominate most of the bronchial tree. Multi-site sequencing in human patients confirms the presence of clonally related preinvasive lesions across distinct airway regions. Our work identifies a transition in basal cell clonal dynamics, and an associated shift in basal cell fate, as drivers of field cancerization in the lung.
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