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Associations of epidemiologic risk factors with Fusobacterium nucleatum and bacterial alpha diversity in the colorectal tumor-associated microbiota

Courtney M. Hill; Rachel C. Malen; Adriana M. Reedy; Orsalem Kahsai; Keith Curtis; Ningxin Ma; Timothy W. Randolph; Jing Ma; Claire E. Thomas; Shuji Ogino; John D. Potter; Daniel D. Buchanan; Polly A. Newcomb; Meredith A. J. Hullar; Amanda I. Phipps
Cancer Causes & Control · Vol. 37, Issue 3 · 2026

Abstract

Background Aspects of the gut microbiome, including presence of specific bacterial species and overall community structure, have been linked to the etiology and prognosis of colorectal cancer (CRC). Less is known about the epidemiologic risk factors that are associated with the composition of the microbiota in invasive colorectal tumors. Methods Using tumor and paired normal colorectal tissue samples from a subset of participants in the population-based Seattle Colon Cancer Family Registry, we compared the presence of Fusobacterium nucleatum (F. nucleatum) ( n = 898) measured via droplet digital PCR and alpha diversity (Shannon index) ( n = 611) measured via 16S rRNA gene sequencing in colorectal tissue across demographics, health behaviors, and neighborhood socioeconomic status (nSES). Results Normalized counts of F. nucleatum were consistently higher in tumor tissue than in patient-matched normal tissue across all risk factors, while alpha diversity was lower. Female sex was associated with high presence and enrichment of F. nucleatum in tumor tissue (odds ratio [OR] 1.61; 95% confidence interval [CI] 1.02, 2.54 and OR 1.58, 95% CI 1.10, 2.27, respectively). Relative to those aged 40–49 years, the youngest age group (< 40 years) had lower alpha diversity in tumor tissue (OR for highest vs. lowest tertile: 0.33; 95% 0.13, 0.83). Other factors, including diet, were not related to F. nucleatum presence or tumor tissue alpha diversity. Conclusion By uncovering epidemiologic risk factors for F. nucleatum presence and bacterial diversity in the intratumoral microbiota, this work informs our understanding of associations of the gut microbiota with CRC etiology and outcomes.

Bibliographic Information

JournalCancer Causes & Control
PublisherSpringer
Publication Date2026-03-01
Publication Year2026
Volume37
Issue3
Document TypeJournal Article
Print ISSN0957-5243
eISSN1573-7225
DOI10.1007/s10552-026-02133-4

Access Information

NARA Access Coverage1990-01-01~Current
Journal Homepagehttps://www.springer.com/journal/10552
Publisher PageOpen Publisher Page
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