Evidence map›Paper›PMID 23936085›Full record

ArticlePloS one2013

Autotaxin signaling governs phenotypic heterogeneity in visceral and parietal mesothelia.

Elaine L Shelton, Cristi L Galindo, Charles H Williams, Elise Pfaltzgraff, Charles C Hong, David M Bader

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

9 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Selective serotonin reuptake inhibitor exposure constricts the mouse ductus arteriosus in utero.American journal of physiology. Heart and circulatory physiology · 2016
    Article
  5. Review
  6. Review
  7. Zebrafish small molecule screens: Taking the phenotypic plunge.Computational and structural biotechnology journal · 2016
    Review
  8. Article
  9. Pleural involvement in lung cancer.Journal of thoracic disease · 2015
    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

6 authors at 1 institution in 1 country.

Elaine L SheltonDepartment of Medicine, Vanderbilt University, Nashville, Tennessee, United States of America.
Cristi L Galindo
Charles H Williams
Elise Pfaltzgraff
Charles C Hong
David M Bader
Vanderbilt University · US

Funding

Training Program in Stem Cell and Regenerative Developmental BiologyT32HD007502 · NICHD · VANDERBILT UNIVERSITY · PI WRIGHT, CHRISTOPHER V · 1997 to 2022
$5.4M
Cardiac Induction by Small Molecule BMP InhibitorsR01HL104040 · NHLBI · VANDERBILT UNIVERSITY · PI HONG, CHARLES C · 2010 to 2014
$2.0M
Chemical Induction of CardiomyogenesisI01BX000771 · VA · VETERANS HEALTH ADMINISTRATION · PI HONG, CHARLES C · 2011 to 2013
–
BLRD VA I01 BX000771NHLBI NIH HHS R01 HL104040NICHD NIH HHS T32 HD007502NIDDK NIH HHS 1R01DK070741-01
6 · The paper itself

Abstract

Mesothelia, which cover all coelomic organs and body cavities in vertebrates, perform diverse functions in embryonic and adult life. Yet, mesothelia are traditionally viewed as simple, uniform epithelia. Here we demonstrate distinct differences between visceral and parietal mesothelia, the most basic subdivision of this tissue type, in terms of gene expression, adhesion, migration, and invasion. Gene profiling determined that autotaxin, a secreted lysophospholipase D originally discovered as a tumor cell-motility-stimulating factor, was expressed exclusively in the more motile and invasive visceral mesothelia and at abnormally high levels in mesotheliomas. Gain and loss of function studies demonstrate that autotaxin signaling is indeed a critical factor responsible for phenotypic differences within mesothelia. Furthermore, we demonstrate that known and novel small molecule inhibitors of the autotaxin signaling pathway dramatically blunt migratory and invasive behaviors of aggressive mesotheliomas. Taken together, this study reveals distinct phenotypes within the mesothelial cell lineage, demonstrates that differential autotaxin expression is the molecular underpinning for these differences, and provides a novel target and lead compounds to intervene in invasive mesotheliomas.

Indexed as

AnimalsCell Line, TumorEpithelial CellsEpitheliumGene ExpressionGenetic HeterogeneityHumansIntestine, SmallLung NeoplasmsLysophospholipase DMesotheliomaMiceMice, TransgenicOmentumPeritoneal NeoplasmsPhenotypeLysophospholipase DPhosphoric Diester Hydrolases

Identifiers

PMID23936085
PMCPMC3723636
OpenAlexW2010716281

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.