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      Alterations of fecal bacterial communities in patients with lung cancer

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          Abstract

          Emerging evidence suggests the microbiome may affect a number of diseases, including lung cancer. However, the direct relationship between gut bacteria and lung cancer remains uncharacterized. In this study, we directly sequenced the hypervariable V1-V2 regions of the 16S rRNA gene in fecal samples from patients with lung cancer and healthy volunteers. Unweighted principal coordinate analysis (PCoA) revealed a clear difference in the bacterial community membership between the lung cancer group and the healthy control group. The lung cancer group had remarkably higher levels of Bacteroidetes, Fusobacteria, Cyanobacteria, Spirochaetes, and Lentisphaerae but dramatically lower levels of Firmicutes and Verrucomicrobia than the healthy control group ( P < 0.05). Despite significant interindividual variation, eight predominant genera were significantly different between the two groups. The lung cancer group had higher levels of Bacteroides, Veillonella, and Fusobacterium but lower levels of Escherichia-Shigella, Kluyvera, Fecalibacterium, Enterobacter, and Dialister than the healthy control group ( P < 0.05). Most notably, correlations between certain specific bacteria and serum inflammatory biomarkers were identified. Our findings demonstrated an altered bacterial community in patients with lung cancer, providing a significant step in understanding the relationship between gut bacteria and lung cancer. To our knowledge, this is the first study to evaluate the correlations between certain specific bacteria and inflammatory indicators. To better understand this relationship, further studies should investigate the underlying mechanisms of gut bacteria in lung cancer animal models.

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          Author and article information

          Journal
          Am J Transl Res
          Am J Transl Res
          ajtr
          American Journal of Translational Research
          e-Century Publishing Corporation
          1943-8141
          2018
          15 October 2018
          : 10
          : 10
          : 3171-3185
          Affiliations
          [1 ] Department of Thoracic Surgery, The Second Hospital of Shandong University Shandong, P. R. China
          [2 ] School of Medicine, Shandong University Jinan 250000, Shandong, P. R. China
          [3 ] Department of Pathology, The Second Hospital of Shandong University Shandong, P. R. China
          [4 ] Cancer Center, The Second Hospital of Shandong University Shandong, P. R. China
          [5 ] Department of Thoracic Surgery, Shandong Provincial Chest Hospital Jinan 250000, Shandong, P. R. China
          Author notes
          Address correspondence to: Xiao-Gang Zhao, Department of Thoracic Surgery, The Second Hospital of Shandong University, Shandong University, 247 Beiyuan Avenue, Jinan 250000, Shandong, P. R. China. Tel: 86-531-85875009; Fax: 86-531-85875009; E-mail: zhaoxiaogang@ 123456sdu.edu.cn
          Article
          PMC6220220 PMC6220220 6220220
          6220220
          30416659
          34d3be27-46bd-4c0d-b7e4-e00982b9421a
          AJTR Copyright © 2018
          History
          : 12 April 2018
          : 07 September 2018
          Categories
          Original Article

          Lung cancer,gut bacteria,carcinogenesis,microbial dysbiosis,16S rRNA gene sequencing

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