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Dysbiosis of the Upper Gastrointestinal Tract in Head-and-Neck Cancer Survivors: A Pilot Study Using the Capsule Sponge Device. | LitMetric

AI Article Synopsis

  • This study investigates the microbiomes of the oral cavity, esophagus, and stomach using different sampling methods in patients with varying risks for esophageal cancer, specifically esophageal squamous cell carcinoma (ESCC).
  • Researchers analyzed samples from 11 patients with pre-cancerous conditions, 21 head and neck cancer survivors, and 40 individuals with functional dyspeptic symptoms, using advanced genetic sequencing techniques.
  • Findings indicate significant differences in microbial diversity and composition across the different patient groups, particularly between functional dyspepsia patients and cancer survivors, but note that the relationship between microbiota changes and treatments for head and neck cancer is still unclear.

Article Abstract

Background: A non-endoscopic capsule-sponge device allows sampling the entire length of the esophagus. Here, we compared microbiomes of the oral cavity, esophagus, and gastric corpus collected by oral swab, capsule-sponge device, and endoscopic biopsy, respectively, in patients representing three distinct risk profiles for esophageal squamous cell carcinoma (ESCC).

Methods: The study enrolled 11 patients with esophageal squamous intraepithelial neoplasia, 21 patients after curative treatment for head and neck squamous cell cancer (HNSCC) (HNSCC survivors), and 40 patients with functional dyspeptic (FD) symptoms. Microbial genomic DNA was analyzed using 16S rRNA gene amplicon sequencing.

Results: The Shannon index of the capsule-sponge sample microbiota was significantly higher in FD group than in patients after treatment for HNSCC, and the Chao index of gastric samples differed between HNSCC survivors and FD patients. Analysis of the β-diversity of FD patients, HNSCC, and esophageal squamous intraepithelial neoplasia showed that different genera formed at each location. The abundance of 205, 116, and 9 genera differed between FD patients and HNSCC survivors in the gastric, capsule-sponge, and oral samples, respectively; 33 genera differed between the FD group and patients with esophageal squamous intraepithelial neoplasia in capsule-sponge samples.

Conclusions: The bacterial communities of the upper digestive tract were clustered according to the anatomic site. Despite substantial differences in gastric and esophageal microbiota samples between FD patients and HNSCC survivors, the microbial members and diversity showed small differences between FD patients and those with esophageal squamous intraepithelial neoplasia. It remains unclear whether gastric and esophageal dysbiosis is associated with or is a consequence of treatment for HNSCC.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11506215PMC
http://dx.doi.org/10.3390/cancers16203528DOI Listing

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