Evidence map›Paper›PMID 29661219›Full record

ArticleMolecular neurodegeneration2018

Modulation of GSK-3 provides cellular and functional neuroprotection in the rd10 mouse model of retinitis pigmentosa.

Alonso Sánchez-Cruz, Beatriz Villarejo-Zori, Miguel Marchena, Josefa Zaldivar-Díez, Valle Palomo, Carmen Gil, Ignacio Lizasoain, Pedro de la Villa, Ana Martínez, Enrique J de la Rosa and 1 more

Open access · goldAbstract read
In one paragraph

Article in Molecular neurodegeneration, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

27 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Article
  3. VP3.15, a dual GSK-3β/PDE7 inhibitor, reduces glioblastoma tumor growth though changes in the tumor microenvironment in a PTEN wild-type context.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2025
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  11. GSK-3β Allosteric Inhibition: A Dead End or a New Pharmacological Frontier?International journal of molecular sciences · 2023
    Review
  12. Article
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  15. Review
  16. Article
  17. Article
  18. Article
  19. A novel mutation inAging · 2021
    Article
  20. International journal of molecular sciences · 2021
    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

11 authors at 3 institutions in 1 country.

Alonso Sánchez-CruzDepartments of Molecular Biomedicine (3D Lab) and Structural and Chemical Biology (IPSBB Unit), Centro de Investigaciones Biológicas-CSIC, C/ Ramiro de Maeztu 9, E-28040, Madrid, Spain.
Beatriz Villarejo-ZoriDepartments of Molecular Biomedicine (3D Lab) and Structural and Chemical Biology (IPSBB Unit), Centro de Investigaciones Biológicas-CSIC, C/ Ramiro de Maeztu 9, E-28040, Madrid, Spain.
Miguel MarchenaDepartments of Molecular Biomedicine (3D Lab) and Structural and Chemical Biology (IPSBB Unit), Centro de Investigaciones Biológicas-CSIC, C/ Ramiro de Maeztu 9, E-28040, Madrid, Spain.
Josefa Zaldivar-DíezDepartments of Molecular Biomedicine (3D Lab) and Structural and Chemical Biology (IPSBB Unit), Centro de Investigaciones Biológicas-CSIC, C/ Ramiro de Maeztu 9, E-28040, Madrid, Spain.
Valle PalomoDepartments of Molecular Biomedicine (3D Lab) and Structural and Chemical Biology (IPSBB Unit), Centro de Investigaciones Biológicas-CSIC, C/ Ramiro de Maeztu 9, E-28040, Madrid, Spain.
Carmen GilDepartments of Molecular Biomedicine (3D Lab) and Structural and Chemical Biology (IPSBB Unit), Centro de Investigaciones Biológicas-CSIC, C/ Ramiro de Maeztu 9, E-28040, Madrid, Spain.
Ignacio LizasoainNeurovascular Research Unit, Department of Pharmacology, Facultad de Medicina, Universidad Complutense de Madrid, Madrid, Spain.
Pedro de la VillaDepartment of Systems Biology, Facultad de Medicina, Universidad de Alcalá, Alcalá de Henares, Spain.
Ana MartínezDepartments of Molecular Biomedicine (3D Lab) and Structural and Chemical Biology (IPSBB Unit), Centro de Investigaciones Biológicas-CSIC, C/ Ramiro de Maeztu 9, E-28040, Madrid, Spain.
Enrique J de la RosaDepartments of Molecular Biomedicine (3D Lab) and Structural and Chemical Biology (IPSBB Unit), Centro de Investigaciones Biológicas-CSIC, C/ Ramiro de Maeztu 9, E-28040, Madrid, Spain.
Catalina Hernández-SánchezDepartments of Molecular Biomedicine (3D Lab) and Structural and Chemical Biology (IPSBB Unit), Centro de Investigaciones Biológicas-CSIC, C/ Ramiro de Maeztu 9, E-28040, Madrid, Spain. chernandez@cib.csic.es.ORCID 0000-0002-0846-5019
Centro de Investigaciones Biológicas Margarita Salas · ESUniversidad Complutense de Madrid · ESUniversidad de Alcalá · ES

Funding

Ministerio de Economía y Competitividad PI13-02098Ministerio de Economía y Competitividad SAF2012-37979-C03-01Ministerio de Economía y Competitividad SAF2013-41059-RMinisterio de Economía y Competitividad SAF2016-75681-RMinisterio de Economía y Competitividad SAF2016-76693-R
6 · The paper itself

Abstract

backgroundRetinitis pigmentosa (RP) is a group of hereditary retinal neurodegenerative conditions characterized by primary dysfunction and death of photoreceptor cells, resulting in visual loss and, eventually, blindness. To date, no effective therapies have been transferred to clinic. Given the diverse genetic etiology of RP, targeting common cellular and molecular retinal alterations has emerged as a potential therapeutic strategy.

methodsUsing the Pde6b

resultsIn rd10 retinas, increased expression of pro-inflammatory markers and reactive gliosis coincided with the early stages of retinal degeneration. Compared with wild-type controls, GSK-3β expression (mRNA and protein) remained unchanged during the retinal degeneration period. However, levels of GSK-3β

conclusionsThese results provide proof of concept of the therapeutic potential of VP3.15 for the treatment of retinal neurodegenerative conditions in general, and RP in particular.

Indexed as

AnimalsApoptosisDisease Models, AnimalGlycogen Synthase Kinase 3 betaMiceMice, Inbred C57BLMice, Mutant StrainsNeuroprotective AgentsRetinaRetinitis PigmentosaThiadiazolesGlycogen Synthase Kinase 3 betaNeuroprotective AgentsThiadiazolesGSK-3Neurodegenerationrd10RetinaRetinitis pigmentosaTherapy

Identifiers

PMID29661219
PMCPMC5902946
OpenAlexW2804073411

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.