Evidence map›Paper›PMID 8710922›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1996

Overexpression of insulin-like growth factor-1 in the heart is coupled with myocyte proliferation in transgenic mice.

K Reiss, W Cheng, A Ferber, J Kajstura, P Li, B Li, G Olivetti, C J Homcy, R Baserga, P Anversa

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 95 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
95citing papers in PubMed, 1 pooled it
9.0field-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

95 citing papers in PubMed, 1 synthesis or guideline pooled it, 293 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Fetal cardiac troponin I levels decline toward birth in sheep.American journal of physiology. Heart and circulatory physiology · 2024
    Article
  4. Implications for neutrophils in cardiac arrhythmias.American journal of physiology. Heart and circulatory physiology · 2024
    Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Determinants of Cardiac Growth and Size.Cold Spring Harbor perspectives in biology · 2020
    Review
  14. Review
  15. Review
  16. Review
  17. Molecular switch model for cardiomyocyte proliferation.Cell regeneration (London, England) · 2019
    Review
  18. Review
  19. Non-sarcomeric causes of heart failure.Biophysical reviews · 2018
    Article
  20. The Role of MicroRNAs in the Cardiac Response to Exercise.Cold Spring Harbor perspectives in medicine · 2017
    Review

35 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

10 authors at 1 institution in 1 country.

K ReissDepartment of Medicine, New York Medical College, Valhalla 10595, USA.
W Cheng
A Ferber
J Kajstura
P Li
B Li
G Olivetti
C J Homcy
R Baserga
P Anversa
New York Medical College · US

Funding

Coronary Vasculature Progenitor Cell in Human Ischemic Heart FailureR01HL039902 · NHLBI · NEW YORK UNIVERSITY · PI ANVERSA, PIERO, KAJSTURA, JAN · 1989 to 2012
$4.7M
OXIDATIVE STRESS AND HEART AGING PHENOTYPE: ISCHEMIAR01HL038132 · NHLBI · NEW YORK MEDICAL COLLEGE · PI ANVERSA, PIERO · 1987 to 2005
$1.5M
POSTINFARCTION DILATED CARDIOMYOPATHYR01HL040561 · NHLBI · NEW YORK MEDICAL COLLEGE · PI ANVERSA, PIERO · 1989 to 1997
–
NHLBI NIH HHS HL-38132NHLBI NIH HHS HL-39902NHLBI NIH HHS HL-40561
6 · The paper itself

Abstract

Transgenic mice were generated in which the cDNA for the human insulin-like growth factor 1B (IGF-1B) was placed under the control of a rat alpha-myosin heavy chain promoter. In mice heterozygous for the transgene, IGF-1B mRNA was not detectable in the fetal heart at the end of gestation, was present in modest levels at 1 day after birth, and increased progressively with postnatal maturation, reaching a peak at 75 days. Myocytes isolated from transgenic mice secreted 1.15 +/- 0.25 ng of IGF-1 per 10(6) cells per 24 hr versus 0.27 +/- 0.10 ng in myocytes from homozygous wild-type littermates. The plasma level of IGF-1 increased 84% in transgenic mice. Heart weight was comparable in wild-type littermates and transgenic mice up to 45 days of age, but a 42%, 45%, 62%, and 51% increase was found at 75, 135, 210, and 300 days, respectively, after birth. At 45, 75, and 210 days, the number of myocytes in the heart was 21%, 31%, and 55% higher, respectively, in transgenic animals. In contrast, myocyte cell volume was comparable in transgenic and control mice at all ages. In conclusion, overexpression of IGF-1 in myocytes leads to cardiomegaly mediated by an increased number of cells in the heart.

Indexed as

AnimalsBase SequenceCell DivisionDNADNA PrimersGene ExpressionHeartHemodynamicsHumansInsulin-Like Growth Factor IMiceMice, TransgenicMolecular Sequence DataMyocardiumMyosinsOrgan SizeDNADNA PrimersInsulin-Like Growth Factor IMyosinsRNA, Messenger

Identifiers

PMID8710922
PMCPMC38724
OpenAlexW2070002301

What OpenQuestion holds

Textmetadata
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.