Evidence map›Paper›PMID 18645009›Full record

ArticleMolecular cancer therapeutics2008

S1P differentially regulates migration of human ovarian cancer and human ovarian surface epithelial cells.

Dongmei Wang, Zhenwen Zhao, Andrea Caperell-Grant, Gong Yang, Samuel C Mok, Jinsong Liu, Robert M Bigsby, Yan Xu

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cancer therapeutics, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

33 citing papers in PubMed, 66 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. A Bioassay Using a Pentadecanal Derivative to Measure S1P Lyase Activity.International journal of molecular sciences · 2021
    Article
  9. Article
  10. SPHK1 Is a Novel Target of Metformin in Ovarian Cancer.Molecular cancer research : MCR · 2019
    Article
  11. Review
  12. Sphingolipid metabolism and drug resistance in ovarian cancer.Cancer drug resistance (Alhambra, Calif.) · 2018
    Article
  13. Nuclear phosphoinositide regulation of chromatin.Journal of cellular physiology · 2018
    Review
  14. Article
  15. Article
  16. "Dicing and Splicing" Sphingosine Kinase and Relevance to Cancer.International journal of molecular sciences · 2017
    Review
  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

8 authors at 3 institutions in 1 country.

Dongmei WangDepartment of Obstetrics and Gynecology, Indiana University, 975 West Walnut Street IB355A, Indianapolis, IN 46202, USA.
Zhenwen Zhao
Andrea Caperell-Grant
Gong Yang
Samuel C Mok
Jinsong Liu
Robert M Bigsby
Yan Xu
Indiana University – Purdue University Indianapolis · USThe University of Texas MD Anderson Cancer Center · USBrigham and Women's Hospital · US

Funding

Novel Lipid Signaling Pathways in Ovarian Cancer CellsR01CA095042 · NCI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI XU, YAN · 2003 to 2007
$1.7M
Novel Bioactive Lipid Receptors in Growth RegulationR01CA089228 · NCI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI XU, YAN · 2002 to 2005
$1.2M
NCI NIH HHS CA-89228NCI NIH HHS R01 CA089228NCI NIH HHS R01 CA095042
6 · The paper itself

Abstract

Epithelial ovarian cancer (EOC) arises from the epithelial layer covering the surface of ovaries and i.p. metastasis is commonly observed at diagnosis. Sphingosine-1-phosphate (S1P), a bioactive lipid signaling molecule, is potentially involved in EOC tumorigenesis. We have found that S1P is elevated in human EOC ascites. We show that physiologically relevant concentrations of S1P stimulate migration and invasion of EOC cells but inhibit migration of human ovarian surface epithelial (HOSE) cells. In addition, S1P inhibits lysophosphatidic acid (LPA)-induced cell migration in HOSE but not in EOC cells. We have provided the first line of evidence that the expression levels of S1P receptor subtypes are not the only determinants for how cells respond to S1P. Although S1P(1) is expressed and functional in HOSE cells, the inhibitory effect mediated by S1P(2) is dominant in those cells. The cellular preexisting stress fibers are also important determinants for the migratory response to S1P. Differential S1P-induced morphology changes are noted in EOC and HOSE cells. Preexisting stress fibers in HOSE cells are further enhanced by S1P treatment, resulting in the negative migratory response to S1P. By contrast, EOC cells lost stress fibers and S1P treatment induces filopodium-like structures at cell edges, which correlates with increased cell motility. In addition, inhibition of the protein kinase C pathway is likely to be involved in the inhibitory effect of S1P on LPA-induced cell migration in HOSE cells. These findings are important for the development of new therapeutics targeting S1P and LPA in EOC.

Indexed as

AscitesCell Line, TumorCell MovementCell ShapeEnzyme ActivationEpithelial CellsExtracellular Signal-Regulated MAP KinasesFemaleHumansLysophospholipidsMitogen-Activated Protein Kinase KinasesOvarian NeoplasmsProtein Kinase CReceptors, LysosphingolipidSignal TransductionSphingosineExtracellular Signal-Regulated MAP Kinaseslysophosphatidic acidLysophospholipidsMitogen-Activated Protein Kinase KinasesProtein Kinase CReceptors, LysosphingolipidSphingosinesphingosine 1-phosphate

Identifiers

PMID18645009
PMCPMC2649755
OpenAlexW2171175765

What OpenQuestion holds

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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.