Evidence map›Paper›PMID 36924298›Full record

ReviewCNS neuroscience & therapeutics2023

FGF/FGFR system in the central nervous system demyelinating disease: Recent progress and implications for multiple sclerosis.

Qingxiang Zhang, Zhiguo Chen, Kaili Zhang, Jie Zhu, Tao Jin

Open access · goldAbstract readReview
In one paragraph

Review in CNS neuroscience & therapeutics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

16 citing papers in PubMed, 21 citations in OpenAlex.

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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 4 institutions in 2 countries.

Qingxiang ZhangNeuroscience Center, Department of Neurology, The First Hospital of Jilin University, Changchun, China.ORCID 0000-0003-4384-5276
Zhiguo ChenCell Therapy Center, Beijing Institute of Geriatrics, National Clinical Research Center for Geriatric Diseases, Xuanwu Hospital, Capital Medical University, Beijing, China.
Kaili ZhangStomatology College of Inner Mongolia Medical University, Hohhot, China.
Jie ZhuNeuroscience Center, Department of Neurology, The First Hospital of Jilin University, Changchun, China.
Tao JinNeuroscience Center, Department of Neurology, The First Hospital of Jilin University, Changchun, China.ORCID 0000-0002-7028-3419
Jilin University · CNInner Mongolia Medical University · CNKarolinska University Hospital · SEMinistry of Education of the People's Republic of China · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWith millions of victims worldwide, multiple sclerosis is the second most common cause of disability among young adults. Although formidable advancements have been made in understanding the disease, the neurodegeneration associated with multiple sclerosis is only partially counteracted by current treatments, and effective therapy for progressive multiple sclerosis remains an unmet need. Therefore, new approaches are required to delay demyelination and the resulting disability and to restore neural function by promoting remyelination and neuronal repair.

aimsThe article reviews the latest literature in this field. MATERIALS AND

methodsThe fibroblast growth factor (FGF) signaling pathway is a promising target in progressive multiple sclerosis. DISCUSSION: FGF signal transduction contributes to establishing the oligodendrocyte lineage, neural stem cell proliferation and differentiation, and myelination of the central nervous system. Furthermore, FGF signaling is implicated in the control of neuroinflammation. In recent years, interventions targeting FGF, and its receptor (FGFR) have been shown to ameliorate autoimmune encephalomyelitis symptoms in multiple sclerosis animal models moderately.

conclusionHere, we summarize the recent findings and investigate the role of FGF/FGFR signaling in the onset and progression, discuss the potential therapeutic advances, and offer fresh insights into managing multiple sclerosis.

Indexed as

Multiple SclerosisAnimalsCell DifferentiationCentral Nervous SystemFibroblast Growth FactorsOligodendrogliaFibroblast Growth Factorsfibroblast growth factor receptorsfibroblast growth factorsinflammationmultiple sclerosisremyelination

Identifiers

PMID36924298
PMCPMC10173727
OpenAlexW4327623569

What OpenQuestion 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 OpenQuestion graph.