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

Authors :
Igor Dolgalev
Hua Zhou
Nina Murrell
Hortense Le
Theodore Sakellaropoulos
Nicolas Coudray
Kelsey Zhu
Varshini Vasudevaraja
Anna Yeaton
Chandra Goparaju
Yonghua Li
Imran Sulaiman
Jun-Chieh J. Tsay
Peter Meyn
Hussein Mohamed
Iris Sydney
Tomoe Shiomi
Sitharam Ramaswami
Navneet Narula
Ruth Kulicke
Fred P. Davis
Nicolas Stransky
Gromoslaw A. Smolen
Wei-Yi Cheng
James Cai
Salman Punekar
Vamsidhar Velcheti
Daniel H. Sterman
J. T. Poirier
Ben Neel
Kwok-Kin Wong
Luis Chiriboga
Adriana Heguy
Thales Papagiannakopoulos
Bettina Nadorp
Matija Snuderl
Leopoldo N. Segal
Andre L. Moreira
Harvey I. Pass
Aristotelis Tsirigos
Source :
Nature Communications, Vol 14, Iss 1, Pp 1-16 (2023)
Publication Year :
2023
Publisher :
Nature Portfolio, 2023.

Abstract

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.

Subjects

Subjects :
Science

Details

Language :
English
ISSN :
20411723
Volume :
14
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Nature Communications
Publication Type :
Academic Journal
Accession number :
edsdoj.326ae301e3024de2b6652801e0ebede8
Document Type :
article
Full Text :
https://doi.org/10.1038/s41467-023-42327-x