Evidence map›Paper›PMID 24472826›Full record

ReviewJournal of molecular and cellular cardiology2014

Myocardial fibroblast-matrix interactions and potential therapeutic targets.

Edie C Goldsmith, Amy D Bradshaw, Michael R Zile, Francis G Spinale

Open access · greenAbstract readReview
In one paragraph

Review in Journal of molecular and cellular cardiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
6.9field-weighted citation impact, top 2% 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

50 citing papers in PubMed, 94 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. The Senescent Heart-"Age Doth Wither Its Infinite Variety".International journal of molecular sciences · 2024
    Review
  12. Article
  13. Review
  14. Article
  15. Cardiac fibroblasts in heart failure and regeneration.Frontiers in cell and developmental biology · 2024
    Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. Cpxm2 as a novel candidate for cardiac hypertrophy and failure in hypertension.Hypertension research : official journal of the Japanese Society of Hypertension · 2022
    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

4 authors at 2 institutions in 1 country.

Edie C GoldsmithDepartment of Cell Biology and Anatomy, University of South Carolina School of Medicine, USA. Electronic address: edie.goldsmith@uscmed.sc.edu.
Amy D BradshawRalph H. Johnson Department of Veteran's Affairs Medical Center, Charleston, SC, USA; Gazes Cardiac Research Institute, Medical University of South Carolina, Charleston, SC, USA.
Michael R ZileRalph H. Johnson Department of Veteran's Affairs Medical Center, Charleston, SC, USA; Gazes Cardiac Research Institute, Medical University of South Carolina, Charleston, SC, USA.
Francis G SpinaleDepartment of Cell Biology and Anatomy, University of South Carolina School of Medicine, USA; Cardiovascular Translational Research Center, University of South Carolina School of Medicine, USA; WJB Dorn Veteran Affairs Medical Center, Columbia, SC, USA.
Medical University of South Carolina · USUniversity of South Carolina · US

Funding

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
Myocardial Protection and Matrix ProteasesR01HL095608 · NHLBI · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI SPINALE, FRANCIS G · 2010 to 2013
$1.4M
Maladaptive Remodeling in Aging MyocardiumI01BX000168 · VA · VETERANS HEALTH ADMINISTRATION · PI SPINALE, FRANCIS G · 2009 to 2024
–
BLRD VA I01 BX000168BLRD VA I01 BX001385NHLBI NIH HHS R01 HL095608NHLBI NIH HHS R01 HL111090
6 · The paper itself

Abstract

The cardiac extracellular matrix (ECM) is a dynamic structure, adapting to physiological and pathological stresses placed on the myocardium. Deposition and organization of the matrix fall under the purview of cardiac fibroblasts. While often overlooked compared to myocytes, fibroblasts play a critical role in maintaining ECM homeostasis under normal conditions and in response to pathological stimuli assume an activated, myofibroblast phenotype associated with excessive collagen accumulation contributing to impaired cardiac function. Complete appreciation of fibroblast function is hampered by the lack of fibroblast-specific reagents and the heterogeneity of fibroblast precursors. This is further complicated by our ability to dissect the role of myofibroblasts versus fibroblasts in myocardial in remodeling. This review highlights critical points in the regulation of collagen deposition by fibroblasts, the current panel of molecular tools used to identify fibroblasts and the role of fibroblast-matrix interactions in fibroblast function and differentiation into the myofibroblast phenotype. The clinical potential of exploiting differences between fibroblasts and myofibroblasts and using them to target specific fibroblast populations is also discussed. This article is part of a Special Issue entitled "Myocyte-Fibroblast Signalling in Myocardium."

Indexed as

Signal TransductionAnimalsCell DifferentiationCollagen Type IDiscoidin Domain ReceptorsExtracellular MatrixFibroblastsFibrosisGene Expression RegulationHumansIntegrinsMolecular Targeted TherapyMyocardiumMyofibroblastsReceptor Protein-Tyrosine KinasesReceptors, MitogenCollagen Type IDiscoidin Domain ReceptorsIntegrinsReceptor Protein-Tyrosine KinasesReceptors, MitogenDiscoidin Domain ReceptorExtracellular matrixFibroblastIntegrinMyofibroblastTransformation

Identifiers

PMID24472826
PMCPMC4005609
OpenAlexW2089759938

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.