Gut microbial diversity and genus-level differences identified in cervical cancer patients versus healthy controls.


Journal

Gynecologic oncology
ISSN: 1095-6859
Titre abrégé: Gynecol Oncol
Pays: United States
ID NLM: 0365304

Informations de publication

Date de publication:
11 2019
Historique:
received: 23 07 2019
revised: 02 09 2019
accepted: 02 09 2019
pubmed: 11 9 2019
medline: 4 12 2019
entrez: 11 9 2019
Statut: ppublish

Résumé

The aim of this study was to characterize variation in the gut microbiome of women with locally advanced cervical cancer and compare it to healthy controls. We characterized the 16S rDNA fecal microbiome in 42 cervical cancer patients and 46 healthy female controls. Shannon diversity index (SDI) was used to evaluate alpha (within sample) diversity. Beta (between sample) diversity was examined using principle coordinate analysis (PCoA) of unweighted Unifrac distances. Relative abundance of microbial taxa was compared between samples using Linear Discriminant Analysis Effect Size (LEfSe). Within cervical cancer patients, bacterial alpha diversity was positively correlated with age (p = 0.22) but exhibited an inverse relationship in control subjects (p < 0.01). Alpha diversity was significantly higher in cervical cancer patients as compared to controls (p < 0.05), though stratification by age suggested this relationship was restricted to older women (>50 years; p < 0.01). Beta diversity (unweighted Unifrac; p < 0.01) also significantly differed between cervical cancer patients and controls. Based on age- and race-adjusted LEfSe analysis, multiple taxa significantly differed between cervical cancer patients and controls. Prevotella, Porphyromonas, and Dialister were significantly enriched in cervical cancer patients, while Bacteroides, Alistipes and members of the Lachnospiracea family were significantly enriched in healthy subjects. Our study suggests differences in gut microbiota diversity and composition between cervical cancer patients and controls. Associations within the gut microbiome by age may reflect etiologic/clinical differences. These findings provide rationale for further study of the gut microbiome in cervical cancer.

Identifiants

pubmed: 31500892
pii: S0090-8258(19)31489-1
doi: 10.1016/j.ygyno.2019.09.002
pmc: PMC6825899
mid: NIHMS1539289
pii:
doi:

Types de publication

Journal Article Multicenter Study Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

237-244

Subventions

Organisme : NCI NIH HHS
ID : P30 CA016672
Pays : United States
Organisme : NCI NIH HHS
ID : T32 CA101642
Pays : United States

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

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Auteurs

Travis T Sims (TT)

Department of Gynecologic Oncology and Reproductive Medicine, Division of Surgery, The University of Texas MD Anderson Cancer Center, Houston, TX, United States of America. Electronic address: ttsims@mdanderson.org.

Lauren E Colbert (LE)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, United States of America.

Jiali Zheng (J)

Department of Epidemiology, The University of Texas MD Anderson Cancer Center, Houston, TX, United States of America.

Andrea Y Delgado Medrano (AY)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, United States of America.

Kristi L Hoffman (KL)

Department of Molecular Virology and Microbiology, Alkek Center for Metagenomics and Microbiome Research, Baylor College of Medicine, Houston, TX, United States of America.

Lois Ramondetta (L)

Department of Gynecologic Oncology and Reproductive Medicine, Division of Surgery, The University of Texas MD Anderson Cancer Center, Houston, TX, United States of America.

Amir Jazaeri (A)

Department of Gynecologic Oncology and Reproductive Medicine, Division of Surgery, The University of Texas MD Anderson Cancer Center, Houston, TX, United States of America.

Anuja Jhingran (A)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, United States of America.

Kathleen M Schmeler (KM)

Department of Gynecologic Oncology and Reproductive Medicine, Division of Surgery, The University of Texas MD Anderson Cancer Center, Houston, TX, United States of America.

Carrie R Daniel (CR)

Department of Epidemiology, The University of Texas MD Anderson Cancer Center, Houston, TX, United States of America.

Ann Klopp (A)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, United States of America.

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Classifications MeSH