Evidence map›Paper›PMID 40311957›Full record

ReviewPharmacological research2025

MMP3 at the crossroads: Linking molecular pathways to disease diagnosis and therapy.

Jing Jiang, Qiong Wu, Snekha Rajasekaran, Rongxue Wu

Abstract readReview
In one paragraph

Review in Pharmacological research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Frontiers in pharmacology · 2026
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Current issues in molecular biology · 2025
    Article
  20. 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.

Jing JiangSection of Cardiology, Department of Medicine, Biological Sciences Division, University of Chicago, Chicago, IL, United States; Binzhou Medical University, Yantai, China.
Qiong WuSection of Cardiology, Department of Medicine, Biological Sciences Division, University of Chicago, Chicago, IL, United States.
Snekha RajasekaranSection of Cardiology, Department of Medicine, Biological Sciences Division, University of Chicago, Chicago, IL, United States.
Rongxue WuSection of Cardiology, Department of Medicine, Biological Sciences Division, University of Chicago, Chicago, IL, United States. Electronic address: rwu3@uchicago.edu.

Funding

Pilot and Feasibility ProgramP30DK020595 · NIDDK · UNIVERSITY OF CHICAGO · PI Matthew J Brady · 2013 to 2026
$20.9M
Re-Engineering Translational Research at the University of ChicagoUL1TR000430 · NCATS · UNIVERSITY OF CHICAGO · PI SOLWAY, JULIAN · 2012 to 2016
$20.2M
ARNT: A novel regulator of cardiac vascular endothelial barrier function in heart failureR01HL140114 · NHLBI · UNIVERSITY OF CHICAGO · PI WU, RONGXUE · 2019 to 2023
$2.1M
NCATS NIH HHS UL1 TR000430NHLBI NIH HHS R01 HL140114NIDDK NIH HHS P30 DK020595
6 · The paper itself

Abstract

Matrix metalloproteinase 3 (MMP-3) is a multifaceted enzyme that plays a critical role in the regulation of extracellular matrix (ECM) dynamics, influencing both normal physiological and pathological processes. In addition to its established role in ECM degradation, MMP-3 is gaining recognition for modulating cellular behaviors such as inflammation, migration, and proliferation. Recent research has uncovered its capacity to activate latent signaling molecules, release growth factors from the ECM and interact with various cell surface receptors, linking MMP-3 to the progression of various diseases, including inflammatory diseases, infection diseases, cardiovascular diseases, neurodegenerative disorders, and cancer. The review provides an overview of MMP-3's molecular regulation, emphasizing the mechanisms controlling its expression and activity. We discuss MMP3's involvement in both ECM-dependent and independent pathways, and its potential as a diagnostic, prognostic biomarker in various diseases. Additionally, we explore therapeutic strategies targeting MMP-3, summarizing ongoing efforts to develop specific inhibitors and modulate its activity in different pathologic conditions. Through this review, we aim to consolidate the diverse functions of MMP-3 and provide new insights into future research directions, particularly in translating these findings into clinical applications.

Indexed as

Matrix Metalloproteinase 3AnimalsExtracellular MatrixHumansMatrix Metalloproteinase InhibitorsNeoplasmsSignal TransductionMatrix Metalloproteinase 3Matrix Metalloproteinase InhibitorsCancerCardiovascular diseasesExtracellular matrix (ECM)Infectious diseasesInflammatory diseasesMatrix metalloproteinase 3 (MMP-3)Neurodegenerative diseases

Identifiers

PMID40311957
PMCPMC13095362

What OpenQuestion holds

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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 OpenQuestion graph.