Evidence map›Paper›PMID 42789554›Full record

ArticlePloS one2026

Tumor microbial biodiversity and microsatellite instability in colorectal cancer.

Calen Mendall, Meredith A J Hullar, Keith R Curtis, Courtney M Hill, Claire E Thomas, Ningxin Ma, Timothy W Randolph, Rachel C Malen, Adriana M Reedy, Scott LaBrie and 4 more

Abstract read
In one paragraph

Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Calen MendallDepartment of Epidemiology, School of Public Health, University of Washington, Seattle, Washington, United States of America.ORCID https://orcid.org/0009-0009-5177-2186
Meredith A J HullarPublic Health Sciences Division, Fred Hutchinson Cancer Center, Seattle, Washington, United States of America.
Keith R CurtisPublic Health Sciences Division, Fred Hutchinson Cancer Center, Seattle, Washington, United States of America.
Courtney M HillDepartment of Epidemiology, School of Public Health, University of Washington, Seattle, Washington, United States of America.
Claire E ThomasPublic Health Sciences Division, Fred Hutchinson Cancer Center, Seattle, Washington, United States of America.ORCID https://orcid.org/0000-0001-9515-3277
Ningxin MaClinical Research Division, Fred Hutchinson Cancer Center, Seattle, Washington, United States of America.ORCID https://orcid.org/0000-0002-4014-5947
Timothy W RandolphClinical Research Division, Fred Hutchinson Cancer Center, Seattle, Washington, United States of America.
Rachel C MalenPublic Health Sciences Division, Fred Hutchinson Cancer Center, Seattle, Washington, United States of America.ORCID https://orcid.org/0009-0006-7262-9029
Adriana M ReedyPublic Health Sciences Division, Fred Hutchinson Cancer Center, Seattle, Washington, United States of America.
Scott LaBriePublic Health Sciences Division, Fred Hutchinson Cancer Center, Seattle, Washington, United States of America.
John D PotterDepartment of Epidemiology, School of Public Health, University of Washington, Seattle, Washington, United States of America.ORCID https://orcid.org/0000-0001-5439-1500
Shuji OginoDepartment of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, Massachusetts, United States of America.
Polly A NewcombPublic Health Sciences Division, Fred Hutchinson Cancer Center, Seattle, Washington, United States of America.
Amanda I PhippsDepartment of Epidemiology, School of Public Health, University of Washington, Seattle, Washington, United States of America.ORCID https://orcid.org/0009-0002-4864-8351

Funding

Data sharing: the Colon Cancer Family Registry CohortU01CA167551 · NCI · UNIVERSITY OF MELBOURNE · PI Daniel David BUCHANAN, Steven Gallinger · 2018 to 2026
$16.8M
Bacterial correlates of colorectal cancer subgroups and survivalR01CA217970 · NCI · UNIVERSITY OF WASHINGTON · PI PHIPPS, AMANDA IRENE · 2018 to 2022
$3.2M
Hormones and Colon Cancer: Epigenetic Subtypes, Risk, and SurvivalR01CA076366 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI NEWCOMB, POLLY A · 1998 to 2009
$2.4M
NCI NIH HHS R01 CA076366NCI NIH HHS R01 CA217970NCI NIH HHS U01 CA167551
6 · The paper itself

Abstract

backgroundGrowing evidence links the gut microbiome to colorectal cancer (CRC) progression, with certain bacterial species enriched in specific molecular tumor subtypes. DNA mismatch repair deficiency in CRC, evidenced by the presence of microsatellite instability (MSI), has been consistently associated with a favorable prognosis, and may be related to certain aspects of the microbiome. Here, we examined the relationship between tumor microbial biodiversity and MSI status.

methodsDiagnostic tumor tissue samples were obtained from the Seattle site of the Colon Cancer Family Registry (SCCFR) and a companion study; both recruited patients diagnosed with incident CRC from 1998 to 2007. MSI status assessment and prokaryotic 16S rRNA gene sequencing was performed on the tumor tissue samples. We used an adaptive test of alpha-diversity (aMiAD) to estimate the association between microbial biodiversity and MSI status. We performed differential abundance analysis with ANCOM-BC to identify enriched genera in tumor tissue, based on dichotomized MSI status. Analyses were adjusted for age, sex, smoking history, and tumor location (N = 632).

resultsThe adaptive aMiAD effect estimate was -1.08 (p = 0.29), suggesting that MSI-high tumors had lower estimated alpha-diversity, though this difference was not statistically significant. We identified 20 differentially abundant genera in CRC tumors according to MSI status, with 8 enriched genera and 12 depleted genera in MSI-high tumors. The most strongly enriched genera in MSI-high tumors were Gemella and Lawsonella, while Sporolactobacillaceae and Cloacibacterium were the most strongly depleted. Fusobacterium was enriched in MSI-high tumors only after subsetting the genus to Fusobacterium nucleatum specific sequences.

conclusionsWe did not detect a statistically significant association between the adaptive alpha-diversity measure and MSI status, though individual measures concordantly estimated a depletion of alpha-diversity in the MSI-high tumors. We found evidence of differential abundance of certain genera dependent on MSI status, including several novel associations.

Indexed as

BiodiversityColorectal NeoplasmsMicrosatellite InstabilityAgedFemaleHumansMaleMiddle AgedRNA, Ribosomal, 16SRNA, Ribosomal, 16S

Identifiers

PMID42789554
PMCPMC13614546

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.