Dysbiosis of the Gut Microbiome is associated with Tumor Biomarkers in Lung Cancer.


Journal

International journal of biological sciences
ISSN: 1449-2288
Titre abrégé: Int J Biol Sci
Pays: Australia
ID NLM: 101235568

Informations de publication

Date de publication:
2019
Historique:
received: 23 04 2019
accepted: 18 07 2019
entrez: 10 10 2019
pubmed: 9 10 2019
medline: 19 5 2020
Statut: epublish

Résumé

Lung cancer is a malignancy with high morbidity and mortality worldwide. More evidences indicated that gut microbiome plays an important role in the carcinogenesis and progression of cancers by metabolism, inflammation and immune response. However, the study about the characterizations of gut microbiome in lung cancer is limited. In this study, the fecal samples were collected from 16 healthy individuals and 30 lung cancer patients who were divided into 3 groups based on different tumor biomarkers (cytokeratin 19 fragment, neuron specific enolase and carcinoembryonic antigen, respectively) and were analyzed using 16S rRNA gene amplicon sequencing. Each lung cancer group has characterized gut microbial community and presents an elimination, low-density, and loss of bacterial diversity microbial ecosystem compared to that of the healthy control. The microbiome structures in family and genera levels are more complex and significantly varied from each group presenting more different and special pathogen microbiome such as

Identifiants

pubmed: 31595156
doi: 10.7150/ijbs.35980
pii: ijbsv15p2381
pmc: PMC6775324
doi:

Substances chimiques

Biomarkers, Tumor 0
RNA, Ribosomal, 16S 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2381-2392

Informations de copyright

© The author(s).

Déclaration de conflit d'intérêts

Competing Interests: The authors have declared that no competing interest exists.

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Auteurs

Fang Liu (F)

Nanjing School of Clinical Medicine, Southern Medical University, Jinling Hospital, Nanjing, 210002, People's Republic of China.

Jingjing Li (J)

Institute of Biotherapy, Southern Medical University, Guangzhou, 510515, People's Republic of China.

Yubin Guan (Y)

Clinical Laboratory, The First Affiliated Hospital of Guangdong Pharmaceutical University, Guangzhou, 510080, People's Republic of China.

Yanfeng Lou (Y)

Nanjing School of Clinical Medicine, Southern Medical University, Jinling Hospital, Nanjing, 210002, People's Republic of China.

Huiying Chen (H)

Institute of Biotherapy, Southern Medical University, Guangzhou, 510515, People's Republic of China.

Mingyu Xu (M)

Institute of Biotherapy, Southern Medical University, Guangzhou, 510515, People's Republic of China.

Dequan Deng (D)

Nanjing School of Clinical Medicine, Southern Medical University, Jinling Hospital, Nanjing, 210002, People's Republic of China.

Jun Chen (J)

Nanjing School of Clinical Medicine, Southern Medical University, Jinling Hospital, Nanjing, 210002, People's Republic of China.

Beibei Ni (B)

Cell-gene Therapy Translational Medicine Research Center, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, 510630, People's Republic of China.

Lan Zhao (L)

Technology center, Guangdong Vitalife Bio-tech Co.,Ltd., Foshan, 528200, People's Republic of China.

Hongwei Li (H)

Institute of Biotherapy, Southern Medical University, Guangzhou, 510515, People's Republic of China.

Hong Sang (H)

Nanjing School of Clinical Medicine, Southern Medical University, Jinling Hospital, Nanjing, 210002, People's Republic of China.

Xiangsheng Cai (X)

Nanjing School of Clinical Medicine, Southern Medical University, Jinling Hospital, Nanjing, 210002, People's Republic of China.
Clinical Laboratory, The First Affiliated Hospital of Guangdong Pharmaceutical University, Guangzhou, 510080, People's Republic of China.

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Classifications MeSH