| Literature DB >> 33177060 |
Jun-Chieh J Tsay1,2, Benjamin G Wu1,2, Imran Sulaiman1, Katherine Gershner3, Rosemary Schluger1, Yonghua Li1, Ting-An Yie1, Peter Meyn4, Evan Olsen1, Luisannay Perez1, Brendan Franca1, Joseph Carpenito1, Tadasu Iizumi1, Mariam El-Ashmawy5, Michelle Badri6, James T Morton7, Nan Shen8, Linchen He9, Gaetane Michaud1, Samaan Rafeq1, Jamie L Bessich1, Robert L Smith2, Harald Sauthoff2, Kevin Felner2, Ray Pillai1, Anastasia-Maria Zavitsanou10, Sergei B Koralov10, Valeria Mezzano10, Cynthia A Loomis10, Andre L Moreira10, William Moore11, Aristotelis Tsirigos10, Adriana Heguy4,10, William N Rom1, Daniel H Sterman1, Harvey I Pass12, Jose C Clemente8, Huilin Li9, Richard Bonneau6,7,13, Kwok-Kin Wong14, Thales Papagiannakopoulos10, Leopoldo N Segal15.
Abstract
In lung cancer, enrichment of the lower airway microbiota with oral commensals commonly occurs, and ex vivo models support that some of these bacteria can trigger host transcriptomic signatures associated with carcinogenesis. Here, we show that this lower airway dysbiotic signature was more prevalent in the stage IIIB-IV tumor-node-metastasis lung cancer group and is associated with poor prognosis, as shown by decreased survival among subjects with early-stage disease (I-IIIA) and worse tumor progression as measured by RECIST scores among subjects with stage IIIB-IV disease. In addition, this lower airway microbiota signature was associated with upregulation of the IL17, PI3K, MAPK, and ERK pathways in airway transcriptome, and we identified Veillonella parvula as the most abundant taxon driving this association. In a KP lung cancer model, lower airway dysbiosis with V. parvula led to decreased survival, increased tumor burden, IL17 inflammatory phenotype, and activation of checkpoint inhibitor markers. SIGNIFICANCE: Multiple lines of investigation have shown that the gut microbiota affects host immune response to immunotherapy in cancer. Here, we support that the local airway microbiota modulates the host immune tone in lung cancer, affecting tumor progression and prognosis.See related commentary by Zitvogel and Kroemer, p. 224.This article is highlighted in the In This Issue feature, p. 211. ©2020 American Association for Cancer Research.Entities:
Mesh:
Year: 2020 PMID: 33177060 PMCID: PMC7858243 DOI: 10.1158/2159-8290.CD-20-0263
Source DB: PubMed Journal: Cancer Discov ISSN: 2159-8274 Impact factor: 38.272