Evidence map›Paper›PMID 24064218›Full record

ArticleThe Journal of biological chemistry2013

ETS-1-mediated transcriptional up-regulation of CD44 is required for sphingosine-1-phosphate receptor subtype 3-stimulated chemotaxis.

Wenliang Zhang, Jiawei Zhao, Jen-Fu Lee, Allison Gartung, Hiba Jawadi, Wanyu Louis Lambiv, Kenneth V Honn, Menq-Jer Lee

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Over Expression of Cancer Stem Cell Marker CD44 and Its Clinical Significance in Patients with Oral Squamous Cell Carcinoma.Indian journal of otolaryngology and head and neck surgery : official publication of the Association of Otolaryngologists of India · 2023
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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 2 institutions in 2 countries.

Wenliang ZhangFrom the Department of Pathology,; the Bioactive Lipid Research Program.
Jiawei ZhaoFrom the Department of Pathology,; the Bioactive Lipid Research Program.
Jen-Fu LeeFrom the Department of Pathology,; the Bioactive Lipid Research Program.
Allison GartungFrom the Department of Pathology,; the Bioactive Lipid Research Program.
Hiba Jawadithe Bioactive Lipid Research Program.
Wanyu Louis LambivFrom the Department of Pathology,; the Bioactive Lipid Research Program.
Kenneth V HonnFrom the Department of Pathology,; the Bioactive Lipid Research Program,; the Karmanos Cancer Institute.
Menq-Jer LeeFrom the Department of Pathology,; the Bioactive Lipid Research Program,; the Karmanos Cancer Institute; the Cardiovascular Research Institute, Wayne State University School of Medicine, Detroit, Michigan 48201. Electronic address: menqjer.lee@wayne.edu.
Active Biotech (Sweden) · SEThe Barbara Ann Karmanos Cancer Institute · US

Funding

PUBLIC HEALTH DEMONSTRATIONP60DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MYERS, MARTIN G · 1985 to 2012
$26.5M
Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Mehboob A Hussain · 2013 to 2026
$24.3M
Sphingolipid Signaling in Endothelial FunctionR01HL071071 · NHLBI · WAYNE STATE UNIVERSITY · PI LEE, MENQ-JER · 2003 to 2012
$2.5M
NHLBI NIH HHS R01 HL 071071NHLBI NIH HHS R01 HL071071NIDDK NIH HHS 5P600-DK020572NIDDK NIH HHS P60 DK020572
6 · The paper itself

Abstract

Sphingosine-1-phosphate (S1P)-regulated chemotaxis plays critical roles in various physiological and pathophysiological conditions. S1P-regulated chemotaxis is mediated by the S1P family of G-protein-coupled receptors. However, molecular details of the S1P-regulated chemotaxis are incompletely understood. Cultured human lung adenocarcinoma cell lines abundantly express S1P receptor subtype 3 (S1P3), thus providing a tractable in vitro system to characterize molecular mechanism(s) underlying the S1P3 receptor-regulated chemotactic response. S1P treatment enhances CD44 expression and induces membrane localization of CD44 polypeptides via the S1P3/Rho kinase (ROCK) signaling pathway. Knockdown of CD44 completely diminishes the S1P-stimulated chemotaxis. Promoter analysis suggests that the CD44 promoter contains binding sites of the ETS-1 (v-ets erythroblastosis virus E26 oncogene homolog 1) transcriptional factor. ChIP assay confirms that S1P treatment stimulates the binding of ETS-1 to the CD44 promoter region. Moreover, S1P induces the expression and nuclear translocation of ETS-1. Knockdown of S1P3 or inhibition of ROCK abrogates the S1P-induced ETS-1 expression. Furthermore, knockdown of ETS-1 inhibits the S1P-induced CD44 expression and cell migration. In addition, we showed that S1P3/ROCK signaling up-regulates ETS-1 via the activity of JNK. Collectively, we characterized a novel signaling axis, i.e., ROCK-JNK-ETS-1-CD44 pathway, which plays an essential role in the S1P3-regulated chemotactic response.

Indexed as

Cell Line, TumorChemotaxisGene Knockdown TechniquesHumansHyaluronan ReceptorsLysophospholipidsMAP Kinase Kinase 4Proto-Oncogene Protein c-ets-1Receptors, Lysosphingolipidrho-Associated KinasesSignal TransductionSphingosineTranscription, GeneticUp-RegulationCD44 protein, humanETS1 protein, humanHyaluronan ReceptorsLysophospholipidsMAP Kinase Kinase 4Proto-Oncogene Protein c-ets-1Receptors, Lysosphingolipidrho-Associated KinasesSphingosinesphingosine 1-phosphateCD44ChemotaxisEts Family Transcription FactorJun N-terminal Kinase (JNK)LipidsReceptorsSignal Transduction

Identifiers

PMID24064218
PMCPMC3820853
OpenAlexW2042757700

What OpenQuestion holds

Textmetadata
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.