Evidence map›Paper›PMID 29149079›Full record

SynthesisInternational journal of molecular sciences2017

Sphingosine 1-phosphate (S1P) signaling in glioblastoma multiforme-A systematic review.

Shailaja Mahajan-Thakur, Sandra Bien-Möller, Sascha Marx, Henry Schroeder, Bernhard H Rauch

Open access · goldAbstract readSystematic Review
In one paragraph

Synthesis in International journal of molecular sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

42 citing papers in PubMed, 59 citations in OpenAlex.

  1. Review
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  19. Targeting the Sphingolipid Rheostat in Gliomas.International journal of molecular sciences · 2022
    Review
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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

5 authors at 1 institution in 1 country.

Shailaja Mahajan-ThakurDepartment of Pharmacology, University Medicine Greifswald, 17487 Greifswald, Germany. mahajan.shailaja@gmail.com.
Sandra Bien-MöllerDepartment of Pharmacology, University Medicine Greifswald, 17487 Greifswald, Germany. sbien@uni-greifswald.de.
Sascha MarxClinic of Neurosurgery, University Medicine Greifswald, 17487 Greifswald, Germany. marxs@uni-greifswald.de.
Henry SchroederClinic of Neurosurgery, University Medicine Greifswald, 17487 Greifswald, Germany. henry.schroeder@uni-greifswald.de.
Bernhard H RauchDepartment of Pharmacology, University Medicine Greifswald, 17487 Greifswald, Germany. Bernhard.Rauch@uni-greifswald.de.ORCID 0000-0002-6003-4662
Universitätsmedizin Greifswald · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The multifunctional sphingosine-1-phosphate (S1P) is a lipid signaling molecule and central regulator in the development of several cancer types. In recent years, intriguing information has become available regarding the role of S1P in the progression of Glioblastoma multiforme (GBM), the most aggressive and common brain tumor in adults. S1P modulates numerous cellular processes in GBM, such as oncogenesis, proliferation and survival, invasion, migration, metastasis and stem cell behavior. These processes are regulated via a family of five G-protein-coupled S1P receptors (S1PR1-5) and may involve mainly unknown intracellular targets. Distinct expression patterns and multiple intracellular signaling pathways of each S1PR subtype enable S1P to exert its pleiotropic cellular actions. Several studies have demonstrated alterations in S1P levels, the involvement of S1PRs and S1P metabolizing enzymes in GBM pathophysiology. While the tumorigenic actions of S1P involve the activation of several kinases and transcription factors, the specific G-protein (Gi, Gq, and G12/13)-coupled signaling pathways and downstream mediated effects in GBM remain to be elucidated in detail. This review summarizes the recent findings concerning the role of S1P and its receptors in GBM. We further highlight the current insights into the signaling pathways considered fundamental for regulating the cellular processes in GMB and ultimately patient prognosis.

Indexed as

AdultBrain NeoplasmsCell MovementDisease ProgressionGlioblastomaGTP-Binding ProteinsHumansLysophospholipidsNeoplasm InvasivenessNeoplasm MetastasisPrognosisReceptors, LysosphingolipidSphingosineGTP-Binding ProteinsLysophospholipidsReceptors, LysosphingolipidSphingosinesphingosine 1-phosphateglioblastoma multiformeS1P receptor signalingsphingosin-1-phosphate

Identifiers

PMID29149079
PMCPMC5713415
OpenAlexW2770691349

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.