Evidence map›Paper›PMID 17678629›Full record

ReviewBiochemical pharmacology2008

Matrix metalloproteinases and their inhibitors in vascular remodeling and vascular disease.

Joseph D Raffetto, Raouf A Khalil

Registry-linked trialOpen access · greenAbstract readReview
In one paragraph

Review in Biochemical pharmacology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03526913 (Role of Platelet Rich Plasma in Enhancing Graft Take in Chronic Venous Ulcers), which is not on this map. Cited by 327 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
327citing papers in PubMed, 2 pooled it
22.1field-weighted citation impact, top 1% of its field
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.

NCT03526913 nacompletednot on this mapstarted 2016, after this paper: background citation

Role of Platelet Rich Plasma in Enhancing Graft Take in Chronic Venous Ulcers

TypeinterventionalSponsorNoha Mohsen OmarRan2016 to 2018Enrolled20ConditionsChronic Venous Hypertension With Ulcer and Inflammation, Chronic Ulcer of Leg or FootArmsPRP, STSG
3 · Its place in the literature

Who cites it

327 citing papers in PubMed, 2 syntheses or guidelines pooled it, 732 citations in OpenAlex.

  1. Type VIII collagen: advances in matrix biology and translational promise.Frontiers in bioengineering and biotechnology · 2025
    Pooled it
  2. Pooled it
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  7. Article
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  15. Mechanobiology and Resolution of Lung Fibrosis.Annual review of physiology · 2026
    Review
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  17. Article
  18. Review
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  20. Review

267 more citing papers are in PubMed but not listed here.

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

2 authors at 2 institutions in 1 country.

Joseph D RaffettoDepartment of Surgery, VA Boston Healthcare System, West Roxbury, MA, United States.
Raouf A Khalil
Brigham and Women's Hospital · USVA Boston Healthcare System · US

Funding

Vascular Mechanisms in Pregnancy-Induced HypertensionR01HL065998 · NHLBI · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI KHALIL, RAOUF A · 2002 to 2016
$4.3M
Vascular Protective Role of Endothelin B ReceptorsR01HL070659 · NHLBI · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI KHALIL, RAOUF A. · 2003 to 2006
$1.2M
NHLBI NIH HHS HL-65998NHLBI NIH HHS HL-70659NHLBI NIH HHS R01 HL065998NHLBI NIH HHS R01 HL070659
6 · The paper itself

Abstract

Matrix metalloproteinases (MMPs) are a family of proteolytic enzymes that degrade various components of the extracellular matrix (ECM). Members of the MMP family include collagenases, gelatinases, stromelysins, matrilysins and membrane-type MMPs. ProMMPs are cleaved into active forms that promote degradation of ECM proteins. Also, recent evidence suggests direct or indirect effects of MMPs on ion channels in the endothelium and vascular smooth muscle, and on other mechanisms of vascular relaxation/contraction. Endogenous tissue inhibitors of metalloproteinases (TIMPs) reduce excessive proteolytic ECM degradation by MMPs. The balance between MMPs and TIMPs plays a major role in vascular remodeling, angiogenesis, and the uterine and systemic vasodilation during normal pregnancy. An imbalance in the MMPs/TIMPs activity ratio may underlie the pathogenesis of vascular diseases such as abdominal aortic aneurysm, varicose veins, hypertension and preeclampsia. Downregulation of MMPs using genetic manipulations of endogenous TIMPs, or synthetic pharmacological inhibitors such as BB-94 (Batimastat) and doxycycline, and Ro-28-2653, a more specific inhibitor of gelatinases and membrane type 1-MMP, could be beneficial in reducing the MMP-mediated vascular dysfunction and the progressive vessel wall damage associated with vascular disease.

Indexed as

AnimalsAortic Aneurysm, AbdominalAtherosclerosisBlood VesselsCoronary RestenosisFemaleHumansHypertensionMatrix Metalloproteinase InhibitorsMatrix MetalloproteinasesNeovascularization, PhysiologicPre-EclampsiaPregnancyTissue Inhibitor of MetalloproteinasesVaricose VeinsVascular DiseasesMatrix Metalloproteinase InhibitorsMatrix MetalloproteinasesTissue Inhibitor of Metalloproteinases

Identifiers

PMID17678629
PMCPMC2254136
OpenAlexW1990653503

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.