Evidence map›Paper›PMID 41106380›Full record

ArticleCancer cell2026

Tumor-infiltrating bacteria disrupt cancer epithelial cell interactions and induce cell-cycle arrest.

Jorge Luis Galeano Niño, Falk Ponath, Victor A Ajisafe, Clara R Becker, Andrew G Kempchinsky, Martha A Zepeda-Rivera, Javier A Gomez, Hanrui Wu, Jessica G Terrazas, Heather Bouzek and 11 more

Abstract read
In one paragraph

Article in Cancer cell, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
–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

25 citing papers in PubMed, 1 synthesis or guideline pooled it.

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  6. IntratumoralJournal for immunotherapy of cancer · 2026
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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

21 authors.

Jorge Luis Galeano NiñoHuman Biology Division, Fred Hutchinson Cancer Center, Seattle, WA, USA; Department of Biological Sciences, University of Texas at El Paso, El Paso, TX, USA.
Falk PonathDepartment of Immunology, James P. Allison Institute, The University of Texas, MD Anderson Cancer Center, Houston, TX, USA.
Victor A AjisafeDepartment of Biological Sciences, University of Texas at El Paso, El Paso, TX, USA.
Clara R BeckerHuman Biology Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Andrew G KempchinskyHuman Biology Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Martha A Zepeda-RiveraDepartment of Immunology, James P. Allison Institute, The University of Texas, MD Anderson Cancer Center, Houston, TX, USA; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA, USA; Department of Genomic Medicine, The University of Texas, MD Anderson Cancer Center, Houston, TX, USA.
Javier A GomezDepartment of Immunology, James P. Allison Institute, The University of Texas, MD Anderson Cancer Center, Houston, TX, USA.
Hanrui WuHuman Biology Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Jessica G TerrazasDepartment of Biological Sciences, University of Texas at El Paso, El Paso, TX, USA.
Heather BouzekDepartment of Genomic Medicine, The University of Texas, MD Anderson Cancer Center, Houston, TX, USA.
Elizabeth CromwellPreclinical Modeling Shared Resources, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Pritha ChananaBioinformatics Shared Resources, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Matthew WongDepartment of Genomic Medicine, The University of Texas, MD Anderson Cancer Center, Houston, TX, USA; Platform for Innovative Microbiome and Translational Research, Department of Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Ashish DamaniaDepartment of Genomic Medicine, The University of Texas, MD Anderson Cancer Center, Houston, TX, USA; Platform for Innovative Microbiome and Translational Research, Department of Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Michael G WhitePlatform for Innovative Microbiome and Translational Research, Department of Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA; Department of Colon & Rectal Surgery, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Y Nancy YouDepartment of Colon & Rectal Surgery, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Scott KopetzDepartment of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Nadim J AjamiDepartment of Genomic Medicine, The University of Texas, MD Anderson Cancer Center, Houston, TX, USA; Platform for Innovative Microbiome and Translational Research, Department of Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Jennifer A WargoDepartment of Genomic Medicine, The University of Texas, MD Anderson Cancer Center, Houston, TX, USA; Platform for Innovative Microbiome and Translational Research, Department of Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA; Department of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Christopher D JohnstonVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA, USA; Department of Genomic Medicine, The University of Texas, MD Anderson Cancer Center, Houston, TX, USA; Platform for Innovative Microbiome and Translational Research, Department of Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Susan BullmanHuman Biology Division, Fred Hutchinson Cancer Center, Seattle, WA, USA; Department of Immunology, James P. Allison Institute, The University of Texas, MD Anderson Cancer Center, Houston, TX, USA; Platform for Innovative Microbiome and Translational Research, Department of Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA; Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA. Electronic address: sbullman@mdanderson.org.

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Eric Collisson · 1985 to 2026
$296.4M
Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI DIANE BODURKA · 1985 to 2026
$290.8M
UTEP Border Biomedical Research CenterU54MD007592 · NIMHD · UNIVERSITY OF TEXAS EL PASO · PI ARSHAD M. KHAN · 2019 to 2026
$35.1M
Interdisciplinary Tranining in Cancer ResearchT32CA080416 · NCI · UNIVERSITY OF WASHINGTON · PI STODDARD, BARRY L. · 1998 to 2023
$9.7M
Build-out of an Imaging and Behavioral Neuroscience Facility for Hispanic Health Disparities at UTEPC06OD032074 · OD · UNIVERSITY OF TEXAS EL PASO · PI KENNEY, MICHAEL J · 2021 to 2021
$5.1M
The SyngenicDNA and μPOET Platform: Overcoming Innate Barriers to Genetic Engineering in Bacteria.R01DE027850 · NIDCR · FRED HUTCHINSON CANCER RESEARCH CENTER · PI JOHNSTON, CHRISTOPHER D · 2017 to 2021
$4.9M
Interrogating the Role of Bacterial Methyl-modifying Enzymes in Pathoadaptation and Host Epigenetic Interference in CancerR01CA290034 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Christopher D Johnston, Angela H Ting · 2024 to 2026
$3.4M
Defining the landscape of bacterial-colonized microniches in tumors and their role in intratumoral heterogeneity.R01CA289812 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Susan Bullman · 2024 to 2026
$3.1M
Deciphering the Critical Determinants of Enteric and Tumor Niche Colonization by Microbes in Colorectal CancerR01CA288827 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Susan Bullman, Christopher D Johnston · 2025 to 2026
$1.4M
The role of Fusobacterium in colorectal cancer treatment, tumor ecology and chemotherapeutic efficacyR00CA229984 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI BULLMAN, SUSAN · 2019 to 2021
$718k
Advanced genetic systems for Fusobacterium nucleatum in oral and extra-oral pathologiesR21DE033533 · NIDCR · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI JOHNSTON, CHRISTOPHER D · 2023 to 2023
$481k
NCI NIH HHS P30 CA015704NCI NIH HHS P30 CA016672NCI NIH HHS R00 CA229984NCI NIH HHS R01 CA288827NCI NIH HHS R01 CA289812NCI NIH HHS R01 CA290034NCI NIH HHS T32 CA080416NIDCR NIH HHS R01 DE027850NIDCR NIH HHS R21 DE033533NIH HHS C06 OD032074NIMHD NIH HHS U54 MD007592
6 · The paper itself

Abstract

Tumor-infiltrating bacteria are increasingly recognized as modulators of cancer progression and therapy resistance. We describe a mechanism by which extracellular intratumoral bacteria, including Fusobacterium, modulate cancer epithelial cell behavior. Spatial imaging and single-cell spatial transcriptomics show that these bacteria predominantly localize extracellularly within tumor microniches of colorectal and oral cancers, characterized by reduced cell density, transcriptional activity, and proliferation. In vitro, Fusobacterium nucleatum disrupts epithelial contacts, inducing G0-G1 arrest and transcriptional quiescence. This state confers 5-fluorouracil resistance and remodels the tumor microenvironment. Findings were validated by live-cell imaging, spatial profiling, mouse models, and a 52-patient colorectal cancer cohort. Transcriptomics reveals downregulation of cell cycle, transcription, and antigen presentation genes in bacteria-enriched regions, consistent with a quiescent, immune-evasive phenotype. In an independent rectal cancer cohort, high Fusobacterium burden correlates with reduced therapy response. These results link extracellular bacteria to cancer cell quiescence and chemoresistance, highlighting microbial-tumor interactions as therapeutic targets.

Indexed as

Cell CommunicationCell Cycle CheckpointsColorectal NeoplasmsEpithelial CellsFusobacterium nucleatumAnimalsCell Line, TumorDrug Resistance, NeoplasmFemaleFluorouracilHumansMiceTumor MicroenvironmentFluorouracilcancer progressioncell-cycle arrestchemoresistancecolorectal cancerepithelial cell-to-cell contactsFusobacteriumhost-pathogen interactionsintratumoral bacterialive-cell confocal imagingspatial single-cell transcriptomicstumor-infiltrating bacteriatumor microenvironment

Identifiers

PMID41106380
PMCPMC12774452

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Registered trials

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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.