Evidence map›Paper›PMID 17556545›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2007

Adipose tissue-specific inactivation of the retinoblastoma protein protects against diabesity because of increased energy expenditure.

Nassim Dali-Youcef, Chikage Mataki, Agnès Coste, Nadia Messaddeq, Sylvain Giroud, Stéphane Blanc, Christian Koehl, Marie-France Champy, Pierre Chambon, Lluis Fajas and 3 more

Open access · greenAbstract readComparative Study
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

53 citing papers in PubMed, 114 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Relevance of pRB Loss in Human Malignancies.Clinical cancer research : an official journal of the American Association for Cancer Research · 2022
    Review
  5. Review
  6. Article
  7. Lower miR-26a levels in breastmilk affect gene expression in adipose tissue of offspring.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
    Article
  8. Article
  9. Article
  10. Article
  11. Emerging Roles for theBiomolecules · 2020
    Review
  12. Loss ofCancers · 2020
    Article
  13. Regulation of E2F1 activity via PKA-mediated phosphorylations.Turkish journal of biology = Turk biyoloji dergisi · 2020
    Article
  14. Review
  15. Article
  16. Review
  17. Dietary Proteins, Brown Fat, and Adiposity.Frontiers in physiology · 2018
    Review
  18. E2F1, a Novel Regulator of Metabolism.Frontiers in endocrinology · 2017
    Review
  19. Article
  20. Review
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

13 authors at 5 institutions in 1 country.

Nassim Dali-YoucefInstitut National de la Santé et de la Recherche Médicale, Centre National de la Recherche Scientifique, Université Louis Pasteur, 1 Rue Laurent Fries, BP 10142, 67404 Illkirch, France.
Chikage Mataki
Agnès Coste
Nadia Messaddeq
Sylvain Giroud
Stéphane Blanc
Christian Koehl
Marie-France Champy
Pierre Chambon
Lluis Fajas
Daniel Metzger
Kristina Schoonjans
Johan Auwerx
Inserm · FRCentre National de la Recherche Scientifique · FRHôpitaux Universitaires de Strasbourg · FRGefluc Languedoc Roussillon · FRInstitut Clinique de la Souris · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The role of the tumor suppressor retinoblastoma protein (pRb) has been firmly established in the control of cell cycle, apoptosis, and differentiation. Recently, it was demonstrated that lack of pRb promotes a switch from white to brown adipocyte differentiation in vitro. We used the Cre-Lox system to specifically inactivate pRb in adult adipose tissue. Under a high-fat diet, pRb-deficient (pRb(ad-/-)) mice failed to gain weight because of increased energy expenditure. This protection against weight gain was caused by the activation of mitochondrial activity in white and brown fat as evidenced by histologic, electron microscopic, and gene expression studies. Moreover, pRb(-/-) mouse embryonic fibroblasts displayed higher proliferation and apoptosis rates than pRb(+/+) mouse embryonic fibroblasts, which could contribute to the altered white adipose tissue morphology. Taken together, our data support a direct role of pRb in adipocyte cell fate determination in vivo and suggest that pRb could serve as a potential therapeutic target to trigger mitochondrial activation in white adipose tissue and brown adipose tissue, favoring an increase in energy expenditure and subsequent weight loss.

Indexed as

Energy MetabolismAdipose Tissue, BrownAdipose Tissue, WhiteAnimalsApoptosisBody WeightCell ProliferationCells, CulturedDietary FatsDNA, MitochondrialFibroblastsGene ExpressionImmunohistochemistryMiceMice, Inbred C57BLObesityDietary FatsDNA, MitochondrialRetinoblastoma Protein

Identifiers

PMID17556545
PMCPMC1965576
OpenAlexW2080748945

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.