肺癌
基因签名
肿瘤促进
生物
肺
肿瘤科
癌症研究
内科学
癌症
表皮生长因子受体
乳腺癌
癌症预防
肿瘤进展
入射(几何)
免疫学
肺癌的治疗
生物信息学
风险因素
肺癌易感性
受体
肿瘤坏死因子α
医学
病理
基因表达
作者
Tej Pandya,Maria Zagorulya,Michelle Leung,Marcellus Augustine,Lydia Liu,Aino‐Maija Leppä,Ulysse Baruchel,Sin Wi Ng,Tamara Klockner,Miriam Mugabo,Anthony Griffen,Oleg Blyuss,Chrysante S. Iliakis,Amalie Grenov,Kerstin Haase,David C. Muller,K Chan,Jincheng Wu,Vernon A. Burk,Neil Wright
出处
期刊:Cell
[Cell Press]
日期:2026-06-01
卷期号:189 (13): 3903-3921.e26
标识
DOI:10.1016/j.cell.2026.05.005
摘要
Predicting lung cancer risk would enhance prevention trials. Although the Canakinumab Anti-inflammatory Thrombosis Outcome Study (CANTOS) trial demonstrated reduced lung cancer incidence with interleukin (IL)-1β inhibition, the high number needed to treat (NNT) to prevent lung cancer limits its use in unselected populations. Using machine learning, we identified a 14-protein plasma signature predicting lung cancer more than 5 years before diagnosis. The signature, validated across eight cohorts, was elevated in current smokers and individuals exposed to particulate matter (PM) and linked to lung myeloid and alveolar cells. In epidermal growth factor receptor ( EGFR )-driven lung adenocarcinoma, diverse epithelial lineages converged on a keratin8 + /claudin4 + alveolar transitional state (KAC), whose transcriptional programs correlated with signature emergence. Components of the signature were induced by PM, oncogenic EGFR , or IL-1β, whereas IL-1β inhibition restrained PM-driven KAC expansion and early tumorigenesis. In CANTOS, the signature identified individuals who seemed to benefit more from anti-IL-1β therapy, lowering the NNT threshold and nominating circulating signals of tumor promotion for prevention.
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