Evidence map›Paper›PMID 12642576›Full record

ArticleThe Journal of biological chemistry2003

Autotaxin is released from adipocytes, catalyzes lysophosphatidic acid synthesis, and activates preadipocyte proliferation. Up-regulated expression with adipocyte differentiation and obesity.

Gilles Ferry, Edwige Tellier, Anne Try, Sandra Grés, Isabelle Naime, Marie Françoise Simon, Marianne Rodriguez, Jérémie Boucher, Ivan Tack, Stéphane Gesta and 7 more

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2003. 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 98 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
98citing papers in PubMed, 1 pooled it
4.8field-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

98 citing papers in PubMed, 1 synthesis or guideline pooled it, 232 citations in OpenAlex.

  1. Pooled it
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  15. Designing Dual Inhibitors of Autotaxin-LPAR GPCR Axis.Molecules (Basel, Switzerland) · 2022
    Review
  16. Article
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  18. Article
  19. Autotaxin-LPA-LPP3 Axis in Energy Metabolism and Metabolic Disease.International journal of molecular sciences · 2021
    Review
  20. Review

38 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

17 authors at 3 institutions in 2 countries.

Gilles FerryInstitut de Recherche Servier, Centre de Recherche de Croissy, 78290 Croissy-sur-Seine, France.
Edwige Tellier
Anne Try
Sandra Grés
Isabelle Naime
Marie Françoise Simon
Marianne Rodriguez
Jérémie Boucher
Ivan Tack
Stéphane Gesta
Pascale Chomarat
Marc Dieu
Martine Raes
Jean Pierre Galizzi
Philippe Valet
Jean A Boutin
Jean Sébastien Saulnier-Blache
Inserm · FRAVL (France) · FRUniversity of Namur · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Our group has recently demonstrated (Gesta, S., Simon, M., Rey, A., Sibrac, D., Girard, A., Lafontan, M., Valet, P., and Saulnier-Blache, J. S. (2002) J. Lipid Res. 43, 904-910) the presence, in adipocyte conditioned-medium, of a soluble lysophospholipase d-activity (LPLDact) involved in synthesis of the bioactive phospholipid lysophosphatidic acid (LPA). In the present report, LPLDact was purified from 3T3F442A adipocyte-conditioned medium and identified as the type II ecto-nucleotide pyrophosphatase phosphodiesterase, autotaxin (ATX). A unique ATX cDNA was cloned from 3T3F442A adipocytes, and its recombinant expression in COS-7 cells led to extracellular release of LPLDact. ATX mRNA expression was highly up-regulated during adipocyte differentiation of 3T3F442A-preadipocytes. This up-regulation was paralleled by the ability of newly differentiated adipocytes to release LPLDact and LPA. Differentiation-dependent up-regulation of ATX expression was also observed in a primary culture of mouse preadipocytes. Treatment of 3T3F442A-preadipocytes with concentrated conditioned medium from ATX-expressing COS-7 cells led to an increase in cell number as compared with concentrated conditioned medium from ATX non-expressing COS-7 cells. The specific effect of ATX on preadipocyte proliferation was completely suppressed by co-treatment with a LPA-hydrolyzing phospholipase, phospholipase B. Finally, ATX expression was found in mature adipocytes isolated from mouse adipose tissue and was substantially increased in genetically obese-diabetic db/db mice when compared with their lean siblings. In conclusion, the present work shows that ATX is responsible for the LPLDact released by adipocytes and exerts a paracrine control on preadipocyte growth via an LPA-dependent mechanism. Up-regulations of ATX expression with adipocyte differentiation and genetic obesity suggest a possible involvement of this released protein in the development of adipose tissue and obesity-associated pathologies.

Indexed as

Multienzyme ComplexesAdipocytesAmino Acid SequenceAnimalsCell DifferentiationCell DivisionCloning, MolecularCOS CellsCulture Media, ConditionedDatabases as TopicDNA, ComplementaryElectrophoresis, Polyacrylamide GelGlucose-6-Phosphate IsomeraseGlycoproteinsLysophospholipase DLysophospholipidsCulture Media, ConditionedDNA, ComplementaryGlucose-6-Phosphate IsomeraseGlycoproteinsLysophospholipase DLysophospholipidsMultienzyme ComplexesPhosphodiesterase IPhosphoric Diester HydrolasesPyrophosphatasesRecombinant ProteinsRNARNA, Messenger

Identifiers

PMID12642576
PMCPMC1885458
OpenAlexW2026202377

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.