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Challenges in Determining the Role of Microbiome Evolution in Barrett's Esophagus and Progression to Esophageal Adenocarcinoma

Journal

MICROORGANISMS
Volume 9, Issue 10, Pages -

Publisher

MDPI
DOI: 10.3390/microorganisms9102003

Keywords

esophageal adenocarcinoma; Barrett's esophagus; Helicobacter pylori; microbiome evolution; esophagus microbiome

Categories

Funding

  1. San Diego Digestive Diseases Research Center [NIH DK120515]
  2. NIH [K23 DK125266, NIH DP1AT010885]
  3. US Dept of Veterans Affairs Award [ICX002027A01]
  4. Moores Cancer Center Support Grant NIH [NCI P30 CA023100]
  5. Mapping host-microbe-metabolite interactions in 3D to find diet-derived enhancers of immunity [NIH 1DP1AT010885]
  6. Advancing our Understanding of Cancer and the Human Microbiome with QIIME 2 [NIH U24CA248454]
  7. National Institutes of Health, USA (NIH grant) [T32GM008806]

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Esophageal adenocarcinoma (EAC) is a deadly disease with a high mortality rate, and its precursor Barrett's esophagus (BE) has been rapidly increasing since the 1970s. Changes in the esophageal microbiome in modern populations may help explain the rise in EAC cases, and non-invasive procedures to detect microbial communities in saliva, oral swabs, and brushings may offer an alternative means of BE detection. Further studies are needed to understand the dynamic changes in microbial communities within BE and their potential causal role in cancer formation.
Esophageal adenocarcinoma (EAC) claims the lives of half of patients within the first year of diagnosis, and its incidence has rapidly increased since the 1970s despite extensive research into etiological factors. The changes in the microbiome within the distal esophagus in modern populations may help explain the growth in cases that other common EAC risk factors together cannot fully explain. The precursor to EAC is Barrett's esophagus (BE), a metaplasia adapted to a reflux-mediated microenvironment that can be challenging to diagnose in patients who do not undergo endoscopic screening. Non-invasive procedures to detect microbial communities in saliva, oral swabs and brushings from the distal esophagus allow us to characterize taxonomic differences in bacterial population abundances within patients with BE versus controls, and may provide an alternative means of BE detection. Unique microbial communities have been identified across healthy esophagus, BE, and various stages of progression to EAC, but studies determining dynamic changes in these communities, including migration from proximal stomach and oral cavity niches, and their potential causal role in cancer formation are lacking. Helicobacter pylori is negatively associated with EAC, and the absence of this species has been implicated in the evolution of chromosomal instability, a main driver of EAC, but joint analyses of microbiome and host genomes are needed. Acknowledging technical challenges, future studies on the prediction of microbial dynamics and evolution within BE and the progression to EAC will require larger esophageal microbiome datasets, improved bioinformatics pipelines, and specialized mathematical models for analysis.

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