Evidence map›Paper›PMID 28988292›Full record

ReviewCellular and molecular life sciences : CMLS2018

Role of cell cycle regulators in adipose tissue and whole body energy homeostasis.

I C Lopez-Mejia, J Castillo-Armengol, S Lagarrigue, L Fajas

Abstract readReview
In one paragraph

Review in Cellular and molecular life sciences : CMLS, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

27 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  14. Comprehensive Analysis of circRNA Expression Profiles in Human Brown Adipose Tissue.Diabetes, metabolic syndrome and obesity : targets and therapy · 2023
    Article
  15. Obesity and endocrine therapy resistance in breast cancer: Mechanistic insights and perspectives.Obesity reviews : an official journal of the International Association for the Study of Obesity · 2022
    Review
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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

4 authors.

I C Lopez-MejiaCenter for Integrative Genomics, University of Lausanne, Lausanne, Switzerland.
J Castillo-ArmengolCenter for Integrative Genomics, University of Lausanne, Lausanne, Switzerland.
S LagarrigueDepartment of Physiology, University of Lausanne, Lausanne, Switzerland.
L FajasCenter for Integrative Genomics, University of Lausanne, Lausanne, Switzerland. lluis.fajas@unil.ch.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the course of the last decades, metabolism research has demonstrated that adipose tissue is not an inactive tissue. Rather, adipocytes are key actors of whole body energy homeostasis. Numerous novel regulators of adipose tissue differentiation and function have been identified. With the constant increase of obesity and associated disorders, the interest in adipose tissue function alterations in the XXIst century has become of paramount importance. Recent data suggest that adipocyte differentiation, adipose tissue browning and mitochondrial function, lipogenesis and lipolysis are strongly modulated by the cell division machinery. This review will focus on the function of cell cycle regulators in adipocyte differentiation, adipose tissue function and whole body energy homeostasis; with particular attention in mouse studies.

Indexed as

Energy MetabolismAdipose TissueAnimalsCell Cycle CheckpointsCell Cycle ProteinsCyclin-Dependent Kinase Inhibitor ProteinsCyclin-Dependent KinasesCyclinsE2F Transcription FactorsHumansCell Cycle ProteinsCyclin-Dependent Kinase Inhibitor ProteinsCyclin-Dependent KinasesCyclinsE2F Transcription FactorsAdipose tissueCDKsCell cycleCyclinsInsulin resistanceMetabolismObesity

Identifiers

PMID28988292
PMCPMC11105252

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.