Evidence map›Paper›PMID 24780447›Full record

ReviewBiochemical pharmacology2014

Targeting matrix metalloproteinases in heart disease: lessons from endogenous inhibitors.

Francis G Spinale, Francisco Villarreal

Abstract readReview
In one paragraph

Review in Biochemical pharmacology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.7field-weighted citation impact, top 6% 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.

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

31 citing papers in PubMed, 67 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Bioactive Compounds and Cardiac Fibrosis: Current Insight and Future Prospect.Journal of cardiovascular development and disease · 2023
    Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Review
  18. Review
  19. Myocardial infarction remodeling that progresses to heart failure: a signaling misunderstanding.American journal of physiology. Heart and circulatory physiology · 2018
    Review
  20. Article
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.

Francis G SpinaleCardiovascular Translational Research Center, University of South Carolina School of Medicine, Columbia, SC, USA; Department of Cell Biology and Anatomy, University of South Carolina School of Medicine, Columbia, SC, USA; WJB Dorn Veteran Affairs Medical Center, Columbia, SC, USA. Electronic address: cvctrc@uscmed.sc.edu.
Francisco VillarrealDivision of Cardiology, University of California-San Diego School of Medicine, La Jolla, CA, USA.
University of California San Diego · USUniversity of South Carolina · US

Funding

Molecular biology and mechanics of the cardiac interstitiumR01HL043617 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI VILLARREAL, FRANCISCO J · 1989 to 2011
$3.5M
Advanced Glycation End-Products in Human MyocardiumR01HL089944 · NHLBI · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI LEWINTER, MARTIN M · 2008 to 2011
$2.6M
Localized Targeting of Matrix Proteases Following Myocardial InfarctionR01HL111090 · NHLBI · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI BURDICK, JASON A, SPINALE, FRANCIS G · 2012 to 2015
$2.0M
Adenosine Mediated Modulation of Cardiac FibrosisR01HL067922 · NHLBI · UNIVERSITY OF CALIFORNIA SAN DIEGO · PI VILLARREAL, FRANCISCO J · 2002 to 2005
$1.4M
Reversal of Myocardial Infarction by Localized StimulationR42HL112519 · NHLBI · MICRO VIDE, LLC · PI SPINALE, FRANCIS G · 2013 to 2015
$1.2M
Maladaptive Remodeling in Aging MyocardiumI01BX000168 · VA · VETERANS HEALTH ADMINISTRATION · PI SPINALE, FRANCIS G · 2009 to 2024
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BLRD VA I01 BX000168NHLBI NIH HHS HL089944NHLBI NIH HHS HL11090NHLBI NIH HHS HL43617NHLBI NIH HHS HL67922NHLBI NIH HHS R01 HL043617NHLBI NIH HHS R01 HL067922NHLBI NIH HHS R01 HL089944NHLBI NIH HHS R01 HL111090NHLBI NIH HHS R42 HL112519
6 · The paper itself

Abstract

Basic pharmacological/transgenic studies have clearly demonstrated a cause-effect relationship between the induction and activation of matrix metalloproteinases (MMPs) and adverse changes in the structure and function of the left ventricle (LV). Thus, regulation of MMP induction and/or activation would appear to be a potential therapeutic target in the context of cardiovascular disease, such as following myocardial infarction (MI). However, pharmacological approaches to inhibit MMPs have yet to be realized for clinical applications. The endogenous inhibitors of the MMPs (TIMPs) constitute a set of 4 small molecules with unique functionality and specificity. Thus, improved understanding on the function and roles of individual TIMPs may provide important insight into the design and targets for pharmacological applications in LV remodeling processes, such as MI. Therefore, the purpose of this review will be to briefly examine biological functions and relevance of the individual TIMPs in terms of adverse LV remodeling post-MI. Second is to examine the past outcomes and issues surrounding clinical trials targeting MMPs in the post MI context and how new insights into TIMP biology may provide new pharmacological targets. This review will put forward the case that initial pharmacological attempts at MMP inhibition were over-simplistic and that future strategies must recognize the diversity of this matrix proteolytic system and that lessons from TIMP biology may lead to future therapeutic strategies.

Indexed as

AnimalsGene Knockout TechniquesHeart DiseasesHumansMatrix MetalloproteinasesMiceMice, TransgenicModels, CardiovascularTissue Inhibitor of MetalloproteinasesVentricular RemodelingMatrix MetalloproteinasesTissue Inhibitor of MetalloproteinasesFibroblastsMyocardial infarctionMyocardial remodelingTissue inhibitors of matrix metalloproteinases

Identifiers

PMID24780447
PMCPMC4060262
OpenAlexW1969504843

What OpenQuestion 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 OpenQuestion graph.