Evidence map›Paper›PMID 18838555›Full record

ArticleThe Journal of cell biology2008

Notch activates cell cycle reentry and progression in quiescent cardiomyocytes.

Víctor M Campa, Raquel Gutiérrez-Lanza, Fabio Cerignoli, Ramón Díaz-Trelles, Brandon Nelson, Toshiya Tsuji, Maria Barcova, Wei Jiang, Mark Mercola

Open access · hybridAbstract read
In one paragraph

Article in The Journal of cell biology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 110 papers.

0numbers the graph read from it
0cells of the map it votes in
110citing papers in PubMed
5.5field-weighted citation impact, top 3% 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

110 citing papers in PubMed, 178 citations in OpenAlex.

  1. A Myocyte-Enriched Long Non-Coding RNA NRMLncR Enhances Myogenesis in Mouse.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  2. Review
  3. Review
  4. bioRxiv : the preprint server for biology · 2026
    Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Review
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  13. Long COVID as a Tauopathy: Of "Brain Fog" and "Fusogen Storms".International journal of molecular sciences · 2023
    Review
  14. Review
  15. Regulation of endogenous cardiomyocyte proliferation: The known unknowns.Journal of molecular and cellular cardiology · 2023
    Review
  16. Article
  17. Cardiac microRNAs: diagnostic and therapeutic potential.Archives of medical science : AMS · 2023
    Article
  18. Review
  19. Article
  20. Article

50 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

9 authors at 2 institutions in 1 country.

Víctor M CampaBurnham Institute for Medical Research, La Jolla, CA 92037, USA.
Raquel Gutiérrez-Lanza
Fabio Cerignoli
Ramón Díaz-Trelles
Brandon Nelson
Toshiya Tsuji
Maria Barcova
Wei Jiang
Mark Mercola
Sanford Burnham Prebys Medical Discovery Institute · USInstitute for Medical Research · US

Funding

Notch function in myocardial development and homeostasisR01HL083463 · NHLBI · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI MERCOLA, MARK · 2006 to 2010
$2.3M
Molecular Biology of Heart InductionR37HL059502 · NHLBI · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI MERCOLA, MARK · 2007 to 2011
$1.6M
NHLBI NIH HHS R01 HL083463NHLBI NIH HHS R01 HL083463-01NHLBI NIH HHS R37 HL059502NHLBI NIH HHS R37 HL059502-01
6 · The paper itself

Abstract

The inability of heart muscle to regenerate by replication of existing cardiomyocytes has engendered considerable interest in identifying developmental or other stimuli capable of sustaining the proliferative capacity of immature cardiomyocytes or stimulating division of postmitotic cardiomyocytes. Here, we demonstrate that reactivation of Notch signaling causes embryonic stem cell-derived and neonatal ventricular cardiomyocytes to enter the cell cycle. The proliferative response of neonatal ventricular cardiomyocytes declines as they mature, such that late activation of Notch triggers the DNA damage checkpoint and G2/M interphase arrest. Notch induces recombination signal-binding protein 1 for Jkappa (RBP-Jkappa)-dependent expression of cyclin D1 but, unlike other inducers, also shifts its subcellular distribution from the cytosol to the nucleus. Nuclear localization of cyclin D1 is independent of RBP-Jkappa. Thus, the influence of Notch on nucleocytoplasmic localization of cyclin D1 is an unanticipated property of the Notch intracellular domain that is likely to regulate the cell cycle in multiple contexts, including tumorigenesis as well as cardiogenesis.

Indexed as

Active Transport, Cell NucleusAnimalsAnimals, NewbornApoptosisBasic Helix-Loop-Helix ProteinsCaffeineCDC2 Protein KinaseCell CycleCell NucleusCell ProliferationCells, CulturedCyclin D1Glycogen Synthase Kinase 3Glycogen Synthase Kinase 3 betaHomeodomain ProteinsImmunoglobulin J Recombination Signal Sequence-Binding ProteinBasic Helix-Loop-Helix ProteinsCaffeineCDC2 Protein KinaseCyclin D1Glycogen Synthase Kinase 3Glycogen Synthase Kinase 3 betaHes1 protein, ratHomeodomain ProteinsImmunoglobulin J Recombination Signal Sequence-Binding ProteinReceptor, Notch2Receptors, NotchRetinoblastoma ProteinTranscription Factor HES-1

Identifiers

PMID18838555
PMCPMC2557048
OpenAlexW2101676313

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.