Evidence map›Paper›PMID 31882542›Full record

ArticleThe Journal of biological chemistry2020

Activation of sphingosine 1-phosphate receptor 2 attenuates chemotherapy-induced neuropathy.

Wei Wang, Ping Xiang, Wee Siong Chew, Federico Torta, Aishwarya Bandla, Violeta Lopez, Wei Lun Seow, Brenda Wan Shing Lam, Jing Kai Chang, Peiyan Wong and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 12% 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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 31 citations in OpenAlex.

  1. Pooled it
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  7. Article
  8. Activation of S1PCell proliferation · 2024
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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

15 authors at 2 institutions in 3 countries.

Wei WangDepartment of Pharmacology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 119228.
Ping XiangDepartment of Pharmacology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 119228.
Wee Siong ChewDepartment of Pharmacology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 119228.
Federico TortaSingapore Lipidomics Incubator (SLING), Yong Loo Lin School of Medicine, National University of Singapore, Singapore 119228.ORCID 0000-0001-7545-7484
Aishwarya BandlaThe N.1 Institute for Health, National University of Singapore, Singapore 119077.
Violeta LopezAlice Lee Centre for Nursing Studies, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 119228.
Wei Lun SeowDepartment of Pharmacology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 119228.
Brenda Wan Shing LamDepartment of Pharmacology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 119228.
Jing Kai ChangDepartment of Pharmacology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 119228.
Peiyan WongNeuroscience Phenotyping Core, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 119228.
Kanokporn ChayaburakulAnatomy Unit, Faculty of Science, Rangsit University, Pathum Thani 12000, Thailand.
Wei-Yi OngDepartment of Anatomy, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 119228.
Markus R WenkSingapore Lipidomics Incubator (SLING), Yong Loo Lin School of Medicine, National University of Singapore, Singapore 119228.
Raghav SundarThe N.1 Institute for Health, National University of Singapore, Singapore 119077 raghav_sundar@nuhs.edu.sg.
Deron R HerrDepartment of Pharmacology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 119228 phcdrh@nus.edu.sg.ORCID 0000-0001-5755-0896
National University of Singapore · SGRangsit University · TH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Platinum-based therapeutics are used to manage many forms of cancer, but frequently result in peripheral neuropathy. Currently, the only option available to attenuate chemotherapy-induced neuropathy is to limit or discontinue this treatment. Sphingosine 1-phosphate (S1P) is a lipid-based signaling molecule involved in neuroinflammatory processes by interacting with its five cognate receptors: S1P

Indexed as

AnimalsAntineoplastic AgentsAxonsBiomarkersCisplatinFemaleHumansLysophospholipidsMyelin SheathNeurogliaPC12 CellsPeripheral Nervous System DiseasesPlatinumRatsRats, Sprague-DawleySignal TransductionAntineoplastic AgentsBiomarkersCisplatinLysophospholipidsPlatinumS1PR2 protein, humanSphingosinesphingosine 1-phosphateSphingosine-1-Phosphate Receptorsanticancer drugcancerchemotherapycisplatinglial cellglial satellite cellsG-protein–coupled receptorneuropathyneuroprotectionoxaliplatinpharmacologysphingosine 1-phosphate (S1P)

Identifiers

PMID31882542
PMCPMC6983853
OpenAlexW2997239061

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.