Accès ouvert déclaré 2025 article

Survival implications of the age-associated tumor and normal adjacent tissue microbiome among colorectal cancer patients

Maria F. Gomez Morales, Stephanie Hogue, Scott Pitcher, Daniel K. Jeong, Ivana Radosavljevic, Amalia J. Stefanou, Seth I. Felder, Jessica R. Burns, Scot E. Dowd, Emily Vogtmann, Rashmi R. Sinha, Liang Wang, X. Wang, Permuth Jennifer B., Cynthia L. Sears, Shaneda Warren Andersen, K. Leigh Greathouse, Jacob K. Kresovich, Mark S. Friedman, Erin M. Siegel, Doratha A. Byrd

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Le résumé fourni par la source

BACKGROUND: CRC incidence is rising among individuals younger than 50 years of age, with significant gaps in our understanding of the composition of the tissue microbiome across the age spectrum. The microbiome of tumors and normal adjacent tissue among colorectal cancer (CRC) patients may provide critical insights into the tumor microenvironment and CRC prognosis. METHODS: We characterized the tumor and normal adjacent tissue microbiome of early-onset (EoCRC, n = 46) and frequency-matched later-onset (LoCRC, N = 101) CRC patients who underwent surgery at Moffitt Cancer Center. We extracted DNA from archival tissue from 147 patients and sequenced the 16 S rRNA gene. We estimated the relative abundance of a priori and exploratory bacteria and alpha and beta diversity. We used multivariable linear regression models to estimate the association of age with the tumor and normal adjacent tissue microbiome. Then, we estimated associations of primarily age-associated microbiome metrics with overall survival using multivariable Cox proportional hazard models. RESULTS: In normal adjacent tissue, for every 10-year increase in age, there was a 1-SD higher relative abundance of a priori-selected Porphyromonas (Beta = 0.14, P = 0.03), Peptostreptococcus (Beta = 0.14, P = 0.03), and Prevotella (Beta = 0.13, P = 0.04). Fusobacterium and Bacillus were more abundant among EoCRC cases than LoCRC cases. In turn, Prevotella was associated with a 47% higher risk of mortality per 1-SD increase (95% CI = 1.19, 1.81; P < 0.001). Fusobacterium was not associated with mortality, but Bacillus was inversely associated with mortality. CONCLUSION: We found that age at diagnosis was associated with the relative abundance of several bacteria, including oral-origin genera that were previously CRC-associated, in CRC normal adjacent tissue. In turn, some of these bacteria were associated with survival, suggesting potential age-related mechanisms underlying associations of the microbiome with survival. TRANSLATIONAL RELEVANCE OF THE WORK: Emerging evidence has highlighted the important role of the microbiome in colorectal cancer (CRC). Since the 1990s, there has been an increase in cases of early-onset colorectal cancer. However, there is still a limited understanding of the risk factors contributing to this rise. Investigating the associations between the microbiome of tumors and normal adjacent tissue in relation to aging offers a unique perspective on potential modifiable factors. Notably, our study has shown that age-related changes in the abundance of bacteria originating from the oral cavity, such as Porphyromonas, Peptostreptococcus, and Prevotella, are linked to CRC prognosis. These findings suggest that changes in the tissue microbiome with age may serve as prognostic markers for CRC and could help inform future prevention strategies that consider dietary and oral health interventions.

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Le contrôle bibliographique ouvert

DOI retrouvé dans Crossref DOI retrouvé ; titre concordant.

Titre Crossref: Survival implications of the age-associated tumor and normal adjacent tissue microbiome among colorectal cancer patients
Date Crossref: 23/12/2025
Éditeur: Springer Science and Business Media LLC
Type: journal-article

Ce recoupement confirme des métadonnées liées au DOI. Il ne confirme ni la méthode ni les conclusions de l’étude, et il ne compte pas comme une seconde source scientifique indépendante.

Où se fait cette recherche

University of South Florida pays non établi dans la notice
Université ou école supérieure
Moffitt Cancer Center pays non établi dans la notice
Établissement de santé
National Cancer Institute Division of Cancer Epidemiology and Genetics pays non établi dans la notice
Organisme public
Johns Hopkins University Department of Molecular Microbiology and Immunology pays non établi dans la notice
Université ou école supérieure
University of Wisconsin Carbone Cancer Center pays non établi dans la notice
Organisme public
University of Wisconsin Health pays non établi dans la notice
Établissement de santé
Wisconsin Division of Public Health pays non établi dans la notice
Établissement de santé
Baylor University Department of Biology pays non établi dans la notice
Université ou école supérieure
College of Public Health pays non établi dans la notice
Université ou école supérieure
Department of Cancer Epidemiology pays non établi dans la notice
Institution
Non-Therapeutic Research Office pays non établi dans la notice
Institution
Department of Gastrointestinal Oncology pays non établi dans la notice
Institution

University of South Florida, Moffitt Cancer Center et Division of Cancer Epidemiology and Genetics — National Cancer Institute, avec 9 autres affiliations.

Une affiliation ne permet pas de déduire la nationalité d’un auteur.

Les sujets associés

Gut microbiota and healthCancer Research and TreatmentsOral microbiology and periodontitis research

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