Evidence map›Paper›PMID 29718989›Full record

ArticlePloS one2018

First evidence of SGPL1 expression in the cell membrane silencing the extracellular S1P siren in mammary epithelial cells.

Nadja Engel, Anna Adamus, Marcus Frank, Karin Kraft, Juliane Kühn, Petra Müller, Barbara Nebe, Annika Kasten, Guido Seitz

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

13 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. SGPL1Cancer gene therapy · 2020
    Article
  12. Article
  13. 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 3 institutions in 1 country.

Nadja EngelDepartment of Pediatric Surgery, University Hospital Marburg, Baldingerstraße, Marburg, Germany.ORCID 0000-0002-6362-9282
Anna AdamusDepartment of Pediatric Surgery, University Hospital Marburg, Baldingerstraße, Marburg, Germany.
Marcus FrankMedical Biology and Electron Microscopy Centre, University Medicine Rostock, Strempelstraße, Rostock, Germany.
Karin KraftComplementary Medicine, Center of Internal Medicine, University Medicine Rostock, Ernst-Heydemann-Straße, Rostock, Germany.
Juliane KühnDepartment of Cell Biology, University Medicine Rostock, Schillingallee, Rostock, Germany.
Petra MüllerDepartment of Cell Biology, University Medicine Rostock, Schillingallee, Rostock, Germany.
Barbara NebeDepartment of Cell Biology, University Medicine Rostock, Schillingallee, Rostock, Germany.
Annika KastenDepartment of Oral and Maxillofacial Surgery, Facial Plastic Surgery, Rostock University Medical Center, Schillingallee, Rostock, Germany.
Guido SeitzDepartment of Pediatric Surgery, University Hospital Marburg, Baldingerstraße, Marburg, Germany.
University of Rostock · DEPhilipps University of Marburg · DEFriedrich-Loeffler-Institut · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The bioactive lipid sphingosine-1-phosphate (S1P) is a main regulator of cell survival, proliferation, motility, and platelet aggregation, and it is essential for angiogenesis and lymphocyte trafficking. In that S1P acts as a second messenger intra- and extracellularly, it might promote cancer progression. The main cause is found in the high S1P concentration in the blood, which encourage cancer cells to migrate through the endothelial barrier into the blood vessels. The irreversible degradation of S1P is solely caused by the sphingosine-1-phosphate lyase (SGPL1). SGPL1 overexpression reduces cancer cell migration and therefore silences the endogenous S1P siren, which promotes cancer cell attraction-the main reason for metastasis. Since our previous metabolomics studies revealed an increased SGPL1 activity in association with successful breast cancer cell treatment in vitro, we further investigated expression and localization of SGPL1. Expression analyses confirmed a very low SGPL1 expression in all breast cancer samples, regardless of their subtype. Additionally, we were able to prove a novel SGPL expression in the cytoplasm membrane of non-tumorigenic breast cells by fusing three independent methods. The general SGPL1 downregulation and the loss of the plasma membrane expression resulted in S1P dependent stimulation of migration in the breast cancer cell lines MCF-7 and BT-20. Not only S1P stimulated migration could be repressed by overexpressing the natural SGPL1 variant not but also more general migratory activity was significantly reduced. Here, for the first time, we report on the SGPL1 plasma membrane location in human, non-malignant breast epithelial cell lines silencing the extracellular S1P siren in vitro, and thereby regulating pivotal cellular functions. Loss of this plasma membrane distribution as well as low SGPL1 expression levels could be a potential prognostic marker and a viable target for therapy. Therefore, the precise role of SGPL1 for cancer treatment should be evaluated.

Indexed as

Aldehyde-LyasesCell Line, TumorCell MembraneEpithelial CellsGene Expression RegulationHumansLysophospholipidsMammary Glands, HumanMCF-7 CellsNeoplasm MetastasisSphingosineAldehyde-LyasesLysophospholipidsSGPL1 protein, humanSphingosinesphingosine 1-phosphate

Identifiers

PMID29718989
PMCPMC5931664
OpenAlexW2802730721

What OpenQuestion holds

Textmetadata
LicenceCC0
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.