Evidence map›Paper›PMID 21421848›Full record

ArticleJournal of lipid research2011

Adipose-specific disruption of autotaxin enhances nutritional fattening and reduces plasma lysophosphatidic acid.

Rodolphe Dusaulcy, Chloé Rancoule, Sandra Grès, Estelle Wanecq, André Colom, Charlotte Guigné, Laurens A van Meeteren, Wouter H Moolenaar, Philippe Valet, Jean Sébastien Saulnier-Blache

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in Journal of lipid research, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04328194 (Autotaxin), which is not on this map. Cited by 104 papers.

0numbers the graph read from it
0cells of the map it votes in
104citing papers in PubMed
4.5field-weighted citation impact, top 4% 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.

NCT04328194 naunknown statusnot on this mapstarted 2021, after this paper: background citation

Autotaxin (ATX) as a Marker for Breast Cancer

TypeinterventionalSponsorAssiut UniversityRan2021 to 2022Enrolled100ConditionsBreast CancerArmsSerum Autotaxin, chest x-ray, Breast ultrasound or mammography, Histopathological examination of breast mass specimens, Magnetic Resonance Imaging ( MRI) and Bone scan
3 · Its place in the literature

Who cites it

104 citing papers in PubMed, 180 citations in OpenAlex.

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  12. microPublication biology · 2024
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  18. Glucagon-like Peptide-1 Secretion Is Inhibited by Lysophosphatidic Acid.International journal of molecular sciences · 2022
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44 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 4 institutions in 2 countries.

Rodolphe DusaulcyInstitut National de la Santé et de la Recherche Médicale (INSERM), U1048, Toulouse, Cedex 4, France; Université de Toulouse, UPS, Institut de Médecine Moléculaire de Rangueil, IFR150, BP84225, Toulouse, France.
Chloé RancouleInstitut National de la Santé et de la Recherche Médicale (INSERM), U1048, Toulouse, Cedex 4, France; Université de Toulouse, UPS, Institut de Médecine Moléculaire de Rangueil, IFR150, BP84225, Toulouse, France.
Sandra GrèsInstitut National de la Santé et de la Recherche Médicale (INSERM), U1048, Toulouse, Cedex 4, France; Université de Toulouse, UPS, Institut de Médecine Moléculaire de Rangueil, IFR150, BP84225, Toulouse, France.
Estelle WanecqInstitut National de la Santé et de la Recherche Médicale (INSERM), U1048, Toulouse, Cedex 4, France; Université de Toulouse, UPS, Institut de Médecine Moléculaire de Rangueil, IFR150, BP84225, Toulouse, France.
André ColomInstitut National de la Santé et de la Recherche Médicale (INSERM), U1048, Toulouse, Cedex 4, France; Université de Toulouse, UPS, Institut de Médecine Moléculaire de Rangueil, IFR150, BP84225, Toulouse, France.
Charlotte GuignéInstitut National de la Santé et de la Recherche Médicale (INSERM), U1048, Toulouse, Cedex 4, France; Université de Toulouse, UPS, Institut de Médecine Moléculaire de Rangueil, IFR150, BP84225, Toulouse, France.
Laurens A van MeeterenDivision of Cell Biology and Center for Biomedical Genetics, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Wouter H MoolenaarDivision of Cell Biology and Center for Biomedical Genetics, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Philippe ValetInstitut National de la Santé et de la Recherche Médicale (INSERM), U1048, Toulouse, Cedex 4, France; Université de Toulouse, UPS, Institut de Médecine Moléculaire de Rangueil, IFR150, BP84225, Toulouse, France.
Jean Sébastien Saulnier-BlacheInstitut National de la Santé et de la Recherche Médicale (INSERM), U1048, Toulouse, Cedex 4, France; Université de Toulouse, UPS, Institut de Médecine Moléculaire de Rangueil, IFR150, BP84225, Toulouse, France. Electronic address: Jean-Sebastien.Saulnier-Blache@inserm.fr.
Inserm · FRUniversité Fédérale de Toulouse Midi-Pyrénées · FRThe Netherlands Cancer Institute · NLUniversité Toulouse III - Paul Sabatier · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autotaxin (ATX) is a secreted lysophospholipase D that generates the lipid mediator lysophosphatidic acid (LPA). ATX is secreted by adipose tissue and its expression is enhanced in obese/insulin-resistant individuals. Here, we analyzed the specific contribution of adipose-ATX to fat expansion associated with nutritional obesity and its consequences on plasma LPA levels. We established ATX(F/F)/aP2-Cre (FATX-KO) transgenic mice carrying a null ATX allele specifically in adipose tissue. FATX-KO mice and their control littermates were fed either a normal or a high-fat diet (HFD) (45% fat) for 13 weeks. FATX-KO mice showed a strong decrease (up to 90%) in ATX expression in white and brown adipose tissue, but not in other ATX-expressing organs. This was associated with a 38% reduction in plasma LPA levels. When fed an HFD, FATX-KO mice showed a higher fat mass and a higher adipocyte size than control mice although food intake was unchanged. This was associated with increased expression of peroxisome proliferator-activated receptor (PPAR)γ2 and of PPAR-sensitive genes (aP2, adiponectin, leptin, glut-1) in subcutaneous white adipose tissue, as well as in an increased tolerance to glucose. These results show that adipose-ATX is a negative regulator of fat mass expansion in response to an HFD and contributes to plasma LPA levels.

Indexed as

AdiposityDisease Models, AnimalLysophospholipidsMultienzyme ComplexesPhosphodiesterase IPyrophosphatasesAdipocytesAdipose Tissue, BrownAdipose Tissue, WhiteAnimalsBlood GlucoseCell SizeDietary FatsFemaleFounder EffectGene DeletionBlood GlucoseDietary FatsInsulinlysophosphatidic acidLysophospholipase DLysophospholipidsMultienzyme ComplexesPhosphodiesterase IPhosphoric Diester HydrolasesPPAR gammaPyrophosphatases

Identifiers

PMID21421848
PMCPMC3090245
OpenAlexW2163881287

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.