Evidence map›Paper›PMID 20197381›Full record

ArticleMolecular cancer research : MCR2010

Autotaxin signaling via lysophosphatidic acid receptors contributes to vascular endothelial growth factor-induced endothelial cell migration.

Malgorzata M Ptaszynska, Michael L Pendrak, Mary L Stracke, David D Roberts

Open access · greenAbstract read
In one paragraph

Article in Molecular cancer research : MCR, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

36 citing papers in PubMed, 68 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Role of Autotaxin in High Glucose-Induced Human ARPE-19 Cells.International journal of molecular sciences · 2022
    Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Lysophosphatidic acid acts on LPABritish journal of pharmacology · 2018
    Article
  14. Role of autotaxin in cancer stem cells.Cancer metastasis reviews · 2018
    Review
  15. Autotaxin⁻Lysophosphatidic Acid Signaling in Alzheimer's Disease.International journal of molecular sciences · 2018
    Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article
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 at 2 institutions in 1 country.

Malgorzata M PtaszynskaLaboratory of Pathology, Center for Cancer Research, National Cancer Institute, Bethesda, MD 20892-1500, USA.
Michael L Pendrak
Mary L Stracke
David D Roberts
National Cancer Institute · USCenter for Cancer Research · US

Funding

Roles of Glycoconjugates and Redox Signaling in Tumor BiologyZIASC009174 · NCI · DIVISION OF CLINICAL SCIENCES - NCI · PI ROBERTS, DAVID D · 2009 to 2024
$4.9M
Regulation of Metastasis and Angiogenesis by Autotaxin and its ProductsZIABC010935 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI STRACKE, MARY · 2009 to 2012
$1.3M
Regulation of Metastasis and Angiogenesis by AutotaxinZ01BC010673 · NCI · BASIC SCIENCES · PI ROBERTS, DAVID D · 2005 to 2007
$165k
Intramural NIH HHS Z01 BC010673Intramural NIH HHS Z99 CA999999Intramural NIH HHS ZIA SC009174
6 · The paper itself

Abstract

Important roles for vascular endothelial growth factor (VEGF) and autotaxin (ATX) have been established for embryonic vasculogenesis and cancer progression. We examined whether these two angiogenic factors cooperate in regulation of endothelial cell migratory responses. VEGF stimulated expression of ATX and LPA1, a receptor for the ATX enzymatic product lysophosphatidic acid (LPA), in human umbilical vein endothelial cells. Knockdown of ATX expression significantly decreased mRNA levels for the receptors LPA1, LPA2, S1P1, S1P2, S1P3, and VEGFR2 and abolished cell migration to lysophosphatidylcholine, LPA, recombinant ATX, and VEGF. Migration to sphingosylphosphorylcholine and sphinogosine-1-phosphate was also reduced in ATX knockdown cells, whereas migration to serum remained unchanged. Furthermore, ATX knockdown decreased Akt2 mRNA levels, whereas LPA treatment strongly stimulated Akt2 expression. We propose that VEGF stimulates LPA production by inducing ATX expression. VEGF also increases LPA1 signaling, which in turn increases Akt2 expression. Akt2 is strongly associated with cancer progression, cellular migration, and promotion of epithelial-mesenchymal transition. These data show a role for ATX in maintaining expression of receptors required for VEGF and lysophospholipids to accelerate angiogenesis. Because VEGF and ATX are upregulated in many cancers, the regulatory mechanism proposed in these studies could apply to cancer-related angiogenesis and cancer progression. These data further suggest that ATX could be a prognostic factor or a target for therapeutic intervention in several cancers.

Indexed as

Cell MovementCells, CulturedEndothelial CellsHumansLysophospholipase DMultienzyme ComplexesNeovascularization, PathologicPhosphodiesterase IPhosphoric Diester HydrolasesProto-Oncogene Proteins c-aktPyrophosphatasesReceptors, Lysophosphatidic AcidReceptors, LysosphingolipidReceptors, Vascular Endothelial Growth FactorRNA InterferenceRNA, MessengerAKT2 protein, humanLysophospholipase DMultienzyme ComplexesPhosphodiesterase IPhosphoric Diester HydrolasesProto-Oncogene Proteins c-aktPyrophosphatasesReceptors, Lysophosphatidic AcidReceptors, LysosphingolipidReceptors, Vascular Endothelial Growth FactorRNA, MessengerVascular Endothelial Growth Factor AVEGFA protein, human

Identifiers

PMID20197381
PMCPMC2841699
OpenAlexW2153704241

What OpenQuestion holds

Textmetadata
LicenceTDM
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.