Lower Airway Dysbiosis Affects Lung Cancer Progression
Author(s) -
Jun-Chieh J. Tsay,
Benjamin G. Wu,
Imran Sulaiman,
Katherine Gershner,
Rosemary Schluger,
Yonghua Li,
Ting-An Yie,
Peter Meyn,
Evan Olsen,
Luisannay Perez,
Brendan Franca,
Joseph Carpenito,
Tadasu Iizumi,
Mariam El-Ashmawy,
Michelle Badri,
James T. Morton,
Nan Shen,
Linchen He,
Gaëtane Michaud,
Samaan Rafeq,
Jamie L. Bessich,
Robert L. Smith,
Harald Sauthoff,
Kevin Felner,
Ray Pillai,
AnastasiaMaria Zavitsanou,
Sergei B. Koralov,
Valeria Mezzano,
Cynthia A. Loomis,
André L. Moreira,
William H. Moore,
Aristotelis Tsirigos,
Adriana Heguy,
William N. Rom,
Daniel H. Sterman,
Harvey I. Pass,
José C. Clemente,
Huilin Li,
Richard Bonneau,
KwokKin Wong,
Thales Papagiannakopoulos,
Leopoldo N. Segal
Publication year - 2020
Publication title -
cancer discovery
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.795
H-Index - 163
eISSN - 2159-8290
pISSN - 2159-8274
DOI - 10.1158/2159-8290.cd-20-0263
Subject(s) - dysbiosis , airway , lung cancer , commensalism , cancer , lung , biology , medicine , immunology , gut flora , pathology , bacteria , genetics , surgery
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 .
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