Inflammation in the tumor-adjacent lung as a predictor of clinical outcome in lung adenocarcinoma

Igor Dolgalev(New York University), Hua Zhou(New York University), Nina Murrell(New York University), Hortense Le(New York University), Theodore Sakellaropoulos(New York University), Nicolas Coudray(New York University), Kelsey Zhu(New York University), Varshini Vasudevaraja(New York University), Anna Yeaton(Broad Institute), Chandra Goparaju(New York University), Yonghua Li(New York University), Imran Sulaiman(New York University), Jun-Chieh J. Tsay(New York University), Peter Meyn(Office of Science), Hussein Mohamed(New York University), Iris Sydney, Tomoe Shiomi, Sitharam Ramaswami(Office of Science), Navneet Narula(New York University), Ruth Kulicke(Celsius Therapeutics (United States)), Fred P. Davis(Celsius Therapeutics (United States)), Nicolas Stransky(Celsius Therapeutics (United States)), Gromoslaw A. Smolen(Celsius Therapeutics (United States)), Wei‐Yi Cheng, James J. Cai, Salman R. Punekar(NYU Langone Health), Vamsidhar Velcheti(NYU Langone Health), Daniel H. Sterman(NYU Langone Health), John T. Poirier(NYU Langone Health), Ben Neel(NYU Langone Health), Kwok‐Kin Wong(NYU Langone Health), Luis Chiriboga(New York University), Adriana Heguy(Office of Science), Thales Papagiannakopoulos(NYU Langone Health), Bettina Nadorp(New York University), Matija Snuderl(NYU Langone Health), Leopoldo N. Segal(NYU Langone Health), André L. Moreira(NYU Langone Health), Harvey I. Pass(NYU Langone Health), Aristotelis Tsirigos(Telio (Norway))
Nature Communications
November 8, 2023
Cited by 28Open Access
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Abstract

Approximately 30% of early-stage lung adenocarcinoma patients present with disease progression after successful surgical resection. Despite efforts of mapping the genetic landscape, there has been limited success in discovering predictive biomarkers of disease outcomes. Here we performed a systematic multi-omic assessment of 143 tumors and matched tumor-adjacent, histologically-normal lung tissue with long-term patient follow-up. Through histologic, mutational, and transcriptomic profiling of tumor and adjacent-normal tissue, we identified an inflammatory gene signature in tumor-adjacent tissue as the strongest clinical predictor of disease progression. Single-cell transcriptomic analysis demonstrated the progression-associated inflammatory signature was expressed in both immune and non-immune cells, and cell type-specific profiling in monocytes further improved outcome predictions. Additional analyses of tumor-adjacent transcriptomic data from The Cancer Genome Atlas validated the association of the inflammatory signature with worse outcomes across cancers. Collectively, our study suggests that molecular profiling of tumor-adjacent tissue can identify patients at high risk for disease progression.


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