Evidence map›Paper›PMID 27357444›Full record

ArticleNature communications2016

Notch-independent RBPJ controls angiogenesis in the adult heart.

Ramón Díaz-Trelles, Maria Cecilia Scimia, Paul Bushway, Danh Tran, Anna Monosov, Edward Monosov, Kirk Peterson, Stacey Rentschler, Pedro Cabrales, Pilar Ruiz-Lozano and 1 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.9field-weighted citation impact, top 10% 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

32 citing papers in PubMed, 61 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Cardiac-targeted delivery of a novel Drp1 inhibitor for acute cardioprotection.Journal of molecular and cellular cardiology plus · 2024
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. TRIM28 regulates sprouting angiogenesis through VEGFR-DLL4-Notch signaling circuit.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2020
    Article
  19. 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

11 authors at 5 institutions in 1 country.

Ramón Díaz-TrellesSanford Burnham Prebys Medical Discovery Institute, La Jolla, California 92037, USA.
Maria Cecilia ScimiaSanford Burnham Prebys Medical Discovery Institute, La Jolla, California 92037, USA.
Paul BushwaySanford Burnham Prebys Medical Discovery Institute, La Jolla, California 92037, USA.
Danh TranSanford Burnham Prebys Medical Discovery Institute, La Jolla, California 92037, USA.
Anna MonosovSanford Burnham Prebys Medical Discovery Institute, La Jolla, California 92037, USA.
Edward MonosovSanford Burnham Prebys Medical Discovery Institute, La Jolla, California 92037, USA.
Kirk PetersonDivision of Cardiology, Department of Medicine, University of California, San Diego, La Jolla, California 92093 USA.
Stacey RentschlerDepartments of Medicine, Developmental Biology and Biomedical Engineering, Washington University, St Louis, Missouri 63110 USA.
Pedro CabralesDepartment of Bioengineering, Jacobs School of Engineering, University of California, San Diego, La Jolla, California 92093 USA.
Pilar Ruiz-LozanoDepartment of Pediatrics, Stanford University, Stanford, California 94305 USA.
Mark MercolaSanford Burnham Prebys Medical Discovery Institute, La Jolla, California 92037, USA.
Sanford Burnham Prebys Medical Discovery Institute · USDiscovery Institute · USUniversity of California, San Diego · USStanford University · USWashington University in St. Louis · US

Funding

Tumor Microenvironment and Cancer ImmunologyP30CA030199 · NCI · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI Michael Jackson · 1985 to 2026
$107.2M
Recombinant HbAp Production for In Vivo Toxicity StudiesP01HL110900 · NHLBI · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI FRIEDMAN, JOEL M · 2012 to 2016
$10.6M
Systems Biology CoreP01HL098053 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI HADDAD, GABRIEL G · 2010 to 2014
$10.2M
WNT SIGNALING IN CARDIAC CONDUCTION AND ARRHYTHMOGENESISR01HL130212 · NHLBI · WASHINGTON UNIVERSITY · PI RENTSCHLER, STACEY LYNN · 2016 to 2024
$4.0M
GENETIC ABLATION OF EPICARDIAL FUNCTION IN THE MOUSER01HL065484 · NHLBI · UNIVERSITY OF CALIFORNIA SAN DIEGO · PI RUIZ-LOZANO, PILAR · 2002 to 2012
$3.7M
BLOOD FLOW AND RHEOLOGY IN THE VENOUS MICROCIRCULATIONR01HL052684 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CABRALES, PEDRO · 1996 to 2011
$3.3M
Role of miR25 in Heart FailureR01HL128072 · NHLBI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI HAJJAR, ROGER J., MERCOLA, MARK · 2015 to 2018
$2.5M
Notch function in myocardial development and homeostasisR01HL083463 · NHLBI · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI MERCOLA, MARK · 2006 to 2010
$2.3M
microRNAs and Integrative Control on Cardiopoiesis - CHANGE OF GRANTEE INSTITUTIOR01HL113601 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI MERCOLA, MARK · 2012 to 2016
$2.2M
Myocardial Angiogenesis and CardioprotectionR01HL108176 · NHLBI · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI MERCOLA, MARK · 2012 to 2015
$1.9M
Genetic Rescue of Retinoid-Induced DysfunctionR01HL086879 · NHLBI · STANFORD UNIVERSITY · PI RUIZ-LOZANO, PILAR · 2009 to 2013
$1.7M
The Role of Notch Signaling in ArrhythmogenesisK08HL107449 · NHLBI · WASHINGTON UNIVERSITY · PI RENTSCHLER, STACEY LYNN · 2011 to 2015
$660k
NCI NIH HHS P30 CA030199NHLBI NIH HHS K08 HL107449NHLBI NIH HHS P01 HL098053NHLBI NIH HHS P01 HL110900NHLBI NIH HHS R01 HL052684NHLBI NIH HHS R01 HL065484NHLBI NIH HHS R01 HL083463NHLBI NIH HHS R01 HL086879NHLBI NIH HHS R01 HL108176NHLBI NIH HHS R01 HL113601NHLBI NIH HHS R01 HL128072NHLBI NIH HHS R01 HL130212NHLBI NIH HHS R56 HL123015
6 · The paper itself

Abstract

Increasing angiogenesis has long been considered a therapeutic target for improving heart function after injury such as acute myocardial infarction. However, gene, protein and cell therapies to increase microvascularization have not been successful, most likely because the studies failed to achieve regulated and concerted expression of pro-angiogenic and angiostatic factors needed to produce functional microvasculature. Here, we report that the transcription factor RBPJ is a homoeostatic repressor of multiple pro-angiogenic and angiostatic factor genes in cardiomyocytes. RBPJ controls angiogenic factor gene expression independently of Notch by antagonizing the activity of hypoxia-inducible factors (HIFs). In contrast to previous strategies, the cardiomyocyte-specific deletion of Rbpj increased microvascularization of the heart without adversely affecting cardiac structure or function even into old age. Furthermore, the loss of RBPJ in cardiomyocytes increased hypoxia tolerance, improved heart function and decreased pathological remodelling after myocardial infarction, suggesting that inhibiting RBPJ might be therapeutic for ischaemic injury.

Indexed as

Neovascularization, PhysiologicAnimalsCoronary VesselsFemaleGene Expression RegulationHEK293 CellsHumansHypoxiaHypoxia-Inducible Factor 1, alpha SubunitImmunoglobulin J Recombination Signal Sequence-Binding ProteinMaleMiceMicrovesselsMyocytes, CardiacParacrine CommunicationHif1a protein, mouseHypoxia-Inducible Factor 1, alpha SubunitImmunoglobulin J Recombination Signal Sequence-Binding ProteinRbpj protein, mouse

Identifiers

PMID27357444
PMCPMC4931341
OpenAlexW2463902587

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.