Evidence map›Paper›PMID 20607468›Full record

ReviewJournal of cardiovascular translational research2010

Protein therapeutics for cardiac regeneration after myocardial infarction.

Vincent F M Segers, Richard T Lee

Open access · greenAbstract readReview
In one paragraph

Review in Journal of cardiovascular translational research, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
9.8field-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

49 citing papers in PubMed, 118 citations in OpenAlex.

  1. Article
  2. Review
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  6. Article
  7. Review
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  9. Article
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  11. Article
  12. Article
  13. Signaling pathways and targeted therapy for myocardial infarction.Signal transduction and targeted therapy · 2022
    Review
  14. GDF15 and Cardiac Cells: Current Concepts and New Insights.International journal of molecular sciences · 2021
    Review
  15. Article
  16. Article
  17. Review
  18. Review
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  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 1 institution in 1 country.

Vincent F M SegersProvasculon Inc., 14 Cambridge Center, Building 1, Cambridge, MA 02142, USA.
Richard T Lee
Harvard University · US

Funding

Interleukin-33 and Myocardial Pressure OverloadR01HL092930 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI LEE, RICHARD T · 2009 to 2013
$2.0M
Aging and Myocardial Progenitor RecruitmentR01AG032977 · NIA · BRIGHAM AND WOMEN'S HOSPITAL · PI LEE, RICHARD T · 2009 to 2013
$1.9M
Endothelial-Cardiomyocyte Interactions and AssemblyR01HL081404 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI LEE, RICHARD T · 2005 to 2008
$1.9M
NHLBI NIH HHS HL092930NHLBI NIH HHS R01 HL081404NHLBI NIH HHS R01 HL092930NIA NIH HHS AG032977NIA NIH HHS R01 AG032977
6 · The paper itself

Abstract

Although most medicines have historically been small molecules, many newly approved drugs are derived from proteins. Protein therapies have been developed for treatment of diseases in almost every organ system, including the heart. Great excitement has now arisen in the field of regenerative medicine, particularly for cardiac regeneration after myocardial infarction. Every year, millions of people suffer from acute myocardial infarction, but the adult mammalian myocardium has limited regeneration potential. Regeneration of the heart after myocardium infarction is therefore an exciting target for protein therapeutics. In this review, we discuss different classes of proteins that have therapeutic potential to regenerate the heart after myocardial infarction. Protein candidates have been described that induce angiogenesis, including fibroblast growth factors and vascular endothelial growth factors, although thus far clinical development has been disappointing. Chemotactic factors that attract stem cells, e.g., hepatocyte growth factor and stromal cell-derived factor-1, may also be useful. Finally, neuregulins and periostin are proteins that induce cell-cycle reentry of cardiomyocytes, and growth factors like IGF-1 can induce growth and differentiation of stem cells. As our knowledge of the biology of regenerative processes and the role of specific proteins in these processes increases, the use of proteins as regenerative drugs could develop as a cardiac therapy.

Indexed as

Regenerative MedicineAngiogenic ProteinsAnimalsCardiovascular AgentsCell DifferentiationCell MovementCell ProliferationHumansMyocardial InfarctionMyocardiumNeovascularization, PhysiologicProteinsRegenerationStem CellsTranslational Research, BiomedicalAngiogenic ProteinsCardiovascular AgentsProteins

Identifiers

PMID20607468
PMCPMC2967710
OpenAlexW2171883456

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.