Evidence map›Paper›PMID 21311773›Full record

ArticlePloS one2011

Cathepsin-D, a key protease in breast cancer, is up-regulated in obese mouse and human adipose tissue, and controls adipogenesis.

Olivier Masson, Christine Prébois, Danielle Derocq, Aline Meulle, Cédric Dray, Danielle Daviaud, Didier Quilliot, Philippe Valet, Catherine Muller, Emmanuelle Liaudet-Coopman

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

24 citing papers in PubMed, 64 citations in OpenAlex.

  1. Review
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  6. Genes · 2022
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  10. Review
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  12. Frontiers in pharmacology · 2019
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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

10 authors at 6 institutions in 1 country.

Olivier MassonIRCM, Institut de Recherche en Cancérologie de Montpellier, Montpellier, France.
Christine Prébois
Danielle Derocq
Aline Meulle
Cédric Dray
Danielle Daviaud
Didier Quilliot
Philippe Valet
Catherine Muller
Emmanuelle Liaudet-Coopman
Institut de Pharmacologie et de Biologie Structurale · FRInstitut de Recherche en Cancérologie de Montpellier · FRUniversité Fédérale de Toulouse Midi-Pyrénées · FRCEA Valduc · FRInserm · FRUniversité Toulouse III - Paul Sabatier · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aspartic protease cathepsin-D (cath-D) is overexpressed by human epithelial breast cancer cells and is closely correlated with poor prognosis in breast cancer. The adipocyte is one of the most prominent cell types in the tumor-microenvironment of breast cancer, and clinical studies have shown that obesity increases the incidence of breast cancer. Here, we provide the first evidence that cath-D expression is up-regulated in adipose tissue from obese human beings, as well as in adipocytes from the obese C57BI6/J mouse. Cath-D expression is also increased during human and mouse adipocyte differentiation. We show that cath-D silencing in 3T3-F442A murine preadipocytes leads to lipid-depleted cells after adipogenesis induction, and inhibits of the expression of PPARγ, HSL and aP2 adipocyte differentiation markers. Altogether, our findings demonstrate the key role of cath-D in the control of adipogenesis, and suggest that cath-D may be a novel target in obesity.

Indexed as

3T3 CellsAdipocytesAdipogenesisAdipose TissueAnimalsBreast NeoplasmsCarcinomaCathepsin DCells, CulturedFatty Acid-Binding ProteinsFemaleGene Expression Regulation, EnzymologicHumansMiceMice, Inbred C57BLObesityCathepsin DFabp4 protein, mouseFatty Acid-Binding ProteinsPeptide HydrolasesPPAR gamma

Identifiers

PMID21311773
PMCPMC3032791
OpenAlexW2079344264

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.