Detailed Characterization of the Lung–Gut Microbiome Axis Reveals the Link between PD-L1 and the Microbiome in Non-Small-Cell Lung Cancer Patients

Author:

Ankudavicius Vytautas1,Nikitina Darja2ORCID,Lukosevicius Rokas2,Tilinde Deimante2,Salteniene Violeta2,Poskiene Lina3,Miliauskas Skaidrius1ORCID,Skieceviciene Jurgita2,Zemaitis Marius1,Kupcinskas Juozas24

Affiliation:

1. Department of Pulmonology, Lithuanian University of Health Sciences, LT-44307 Kaunas, Lithuania

2. Institute for Digestive Research, Lithuanian University of Health Sciences, LT-44307 Kaunas, Lithuania

3. Department of Pathology, Lithuanian University of Health Sciences, LT-44307 Kaunas, Lithuania

4. Department of Gastroenterology, Lithuanian University of Health Sciences, LT-44307 Kaunas, Lithuania

Abstract

Next-generation sequencing technologies have started a new era of respiratory tract research in recent years. Alterations in the respiratory microbiome between healthy and malignant conditions have been revealed. However, the composition of the microbiome varies among studies, even in similar medical conditions. Also, there is a lack of complete knowledge about lung–gut microbiome interactions in lung cancer patients. The aim of this study was to explore the lung–gut axis in non-small-cell lung cancer (NSCLC) patients and the associations between lung–gut axis microbiota and clinical parameters (CRP, NLR, LPS, CD8, and PD-L1). Lung tissue and fecal samples were used for bacterial 16S rRNA sequencing. The results revealed, for the first time, that the bacterial richness in lung tumor tissue gradually decreased with an increase in the level of PD-L1 expression (p < 0.05). An analysis of β-diversity indicated a significant positive correlation between the genera Romboutsia and Alistipes in both the lung tumor biopsies and stool samples from NSCLC patients (p < 0.05). Survival analysis showed that NSCLC patients with higher bacterial richness in their stool samples had prolonged overall survival (HR: 2.06, 95% CI: 1.025–4.17, p = 0.0426).

Publisher

MDPI AG

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