Evidence map›Paper›PMID 21321095›Full record

ArticleJournal of molecular endocrinology2011

Pharmacological inhibition of sphingosine kinase isoforms alters estrogen receptor signaling in human breast cancer.

James W Antoon, William D Meacham, Melyssa R Bratton, Evelyn M Slaughter, Lyndsay V Rhodes, Hasina B Ashe, Thomas E Wiese, Matthew E Burow, Barbara S Beckman

Open access · bronzeAbstract read
In one paragraph

Article in Journal of molecular endocrinology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
4.0field-weighted citation impact, top 5% 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

32 citing papers in PubMed, 49 citations in OpenAlex.

  1. Trial
  2. Article
  3. Emerging Roles of Ceramides in Breast Cancer Biology and Therapy.International journal of molecular sciences · 2022
    Review
  4. Review
  5. Targeting Sphingolipids for Cancer Therapy.Frontiers in oncology · 2021
    Review
  6. Article
  7. Review
  8. Review
  9. Sphingolipid metabolism and drug resistance in ovarian cancer.Cancer drug resistance (Alhambra, Calif.) · 2018
    Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Sphingosine kinase 1 isoform-specific interactions in breast cancer.Molecular endocrinology (Baltimore, Md.) · 2014
    Article
  16. Article
  17. Article
  18. Article
  19. Review
  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

9 authors at 2 institutions in 1 country.

James W AntoonTulane Department of Pharmacology Section of Hematology and Medical Oncology, Tulane Department of Medicine, Tulane University School of Medicine, 1430 Tulane Avenue, SL-83, New Orleans, Louisiana 70112, USA.
William D Meacham
Melyssa R Bratton
Evelyn M Slaughter
Lyndsay V Rhodes
Hasina B Ashe
Thomas E Wiese
Matthew E Burow
Barbara S Beckman
Tulane University · USXavier University of Louisiana · US

Funding

P13K/AKT crosstalk with ER-signaling and cell survivalR01DK059389 · NIDDK · TULANE UNIVERSITY OF LOUISIANA · PI BUROW, MATTHEW E. · 2003 to 2008
$1.8M
NIDDK NIH HHS R01 DK059389
6 · The paper itself

Abstract

Recently, crosstalk between sphingolipid signaling pathways and steroid hormones has been illuminated as a possible therapeutic target. Sphingosine kinase (SK), the key enzyme metabolizing pro-apoptotic ceramide to pro-survival sphingosine-1-phosphate (S1P), is a promising therapeutic target for solid tumor cancers. In this study, we examined the ability of pharmacological inhibition of S1P formation to block estrogen signaling as a targeted breast cancer therapy. We found that the Sphk1/2 selective inhibitor (SK inhibitor (SKI))-II, blocked breast cancer viability, clonogenic survival and proliferation. Furthermore, SKI-II dose-dependently decreased estrogen-stimulated estrogen response element transcriptional activity and diminished mRNA levels of the estrogen receptor (ER)-regulated genes progesterone receptor and steroid derived factor-1. This inhibitor binds the ER directly in the antagonist ligand-binding domain. Taken together, our results suggest that SKIs have the ability to act as novel ER signaling inhibitors in breast carcinoma.

Indexed as

Blotting, WesternBreast NeoplasmsCell Line, TumorCell ProliferationCell SurvivalComputer SimulationEstrogen Receptor alphaHumansIsoenzymesMass SpectrometryPhosphotransferases (Alcohol Group Acceptor)Reverse Transcriptase Polymerase Chain ReactionSignal TransductionSphingosine KinaseThiazoles4-(4-(4-chloro-phenyl)thiazol-2-ylamino)phenolESR1 protein, humanEstrogen Receptor alphaIsoenzymesPhosphotransferases (Alcohol Group Acceptor)Sphingosine KinaseThiazoles

Identifiers

PMID21321095
PMCPMC4007162
OpenAlexW2159775348

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.