Evidence map›Paper›PMID 40796163›Full record

ReviewJournal of leukocyte biology2025

The function of metalloproteinases in pathophysiology of inflammatory bowel disease and colon cancer.

Laura D Manzanares, Caroline J Herrnreiter, Joseph Hirst, Ronen Sumagin

Abstract readReview
In one paragraph

Review in Journal of leukocyte biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Effects of personalized vitamin DBritish journal of cancer · 2026
    Trial
  2. Review
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

4 authors.

Laura D ManzanaresDepartment of Pathology, Feinberg School of Medicine, Northwestern University, 300 East Superior Street, Chicago, IL 60611, United States.ORCID 0000-0003-0806-5186
Caroline J HerrnreiterDepartment of Pathology, Feinberg School of Medicine, Northwestern University, 300 East Superior Street, Chicago, IL 60611, United States.ORCID 0000-0002-6345-3758
Joseph HirstDivision of Gastroenterology, Hepatology and Nutrition, Ann and Robert H. Lurie Children's Hospital of Chicago, 225 East Chicago Avenue, Chicago, IL 60611, United States.ORCID 0009-0006-9598-2159
Ronen SumaginDepartment of Pathology, Feinberg School of Medicine, Northwestern University, 300 East Superior Street, Chicago, IL 60611, United States.ORCID 0000-0002-5689-1100

Funding

Tumor Environment and Metastasis (TEAM) Research ProgramP30CA060553 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Devalingam Mahalingam · 1993 to 2026
$153.9M
Identifying Neutrophil Specific Mechanisms for Resistance to Biologics in Ulcerative ColitisR01DK135620 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Parambir Singh Dulai, Ronen Sumagin · 2023 to 2026
$2.7M
Vascular endothelial cells and macrophages coordinate neutrophil trafficking in inflammationR01AI153568 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI SUMAGIN, RONEN · 2021 to 2025
$1.9M
Neutrophils instruct macrophage responses to promote mucosal healingR01DK124199 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI SUMAGIN, RONEN · 2020 to 2023
$1.4M
National Institute of Allergy and infectious Diseases AI153568National Institute of Allergy and infectious Diseases DK124199National Institutes of Health National Institute of Diabetes and Digestive and Kidney DiseasesNCI NIH HHS P30 CA060553NCI NIH HHS P30-CA060553NIAID NIH HHS R01 AI153568NIDDK NIH HHS R01 DK124199NIDDK NIH HHS R01 DK135620Northwestern University Mouse Histology and Phenotyping LaboratoryRobert H. Lurie Comprehensive Cancer Center
6 · The paper itself

Abstract

Inflammatory bowel disease (IBD) is a debilitating and symptomatic disorder of the gastrointestinal tract, featuring dysregulated inflammation, intestinal injury, and barrier dysfunction. IBD is also a risk factor for colorectal cancer (CRC), which remains a leading cause of cancer-related mortalities worldwide. Matrix metalloproteinases (MMPs) are a diverse family of proteases that play critical roles in both intestinal homeostasis and disease pathogenesis. Produced by epithelial, stromal, and immune cells, MMPs can regulate stem cell function, immune cell recruitment, microbial composition, barrier integrity, angiogenesis, and cell proliferation through extracellular matrix remodeling, cytokine activation, or direct interactions with target cells, thereby impacting the progression of both IBD and CRC. In this review we discuss the roles of MMPs in the maintenance of intestinal homeostasis and their contributions to imbalanced immune responses, epithelial integrity, and wound healing in IBD. Additionally, we highlight their contribution to epithelial-to-mesenchymal transition, angiogenesis, and metastasis in CRC. Finally, we review the potential utilization of MMPs as biomarkers for IBD/CRC diagnosis, prognosis, and treatment response. MMPs remain central to both IBD and CRC biology and present both challenges and opportunities for therapeutic intervention and disease monitoring.

Indexed as

Colonic NeoplasmsInflammatory Bowel DiseasesMatrix MetalloproteinasesMetalloproteasesAnimalsEpithelial-Mesenchymal TransitionHumansNeovascularization, PathologicMatrix MetalloproteinasesMetalloproteasesepithelial barrierimmunotherapyinflammationinflammatory bowel diseasewound healing

Identifiers

PMID40796163
PMCPMC12459279

What Socratic holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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 Socratic graph.