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Lower Airway Dysbiosis Affects Lung Cancer Progression.

Jun-Chieh J TsayBenjamin G WuImran SulaimanKatherine GershnerRosemary SchlugerYonghua LiTing-An YiePeter MeynEvan OlsenLuisannay PerezBrendan FrancaJoseph CarpenitoTadasu IizumiMariam El-AshmawyMichelle BadriJames T MortonNan ShenLinchen HeGaetane MichaudSamaan RafeqJamie L BessichRobert L SmithHarald SauthoffKevin FelnerRay G PillaiAnastasia-Maria ZavitsanouSergei B KoralovValeria MezzanoCynthia A LoomisAndre L MoreiraWilliam MooreAristotelis TsirigosAdriana HeguyWilliam N RomDaniel H StermanHarvey I PassJose C ClementeHuilin LiRichard BonneauKwok-Kin WongThales PapagiannakopoulosLeopoldo N Segal
Published in: Cancer discovery (2020)
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.
Keyphrases
  • poor prognosis
  • early stage
  • long non coding rna
  • signaling pathway
  • cell proliferation
  • oxidative stress
  • single cell
  • lymph node
  • gene expression
  • rna seq
  • deep learning
  • dna damage
  • young adults
  • free survival
  • drug induced