Evidence map›Paper›PMID 33918666›Full record

ReviewInternational journal of molecular sciences2021

JNK Pathway in CNS Pathologies.

Teresa de Los Reyes Corrales, María Losada-Pérez, Sergio Casas-Tintó

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
–field-weighted citation impact
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

54 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Gender-specific gene profiling inIBRO neuroscience reports · 2026
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Thermally Gated Dual-Cascade Nanozyme for Enhanced Mild-Temperature Photothermal Therapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
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  16. medRxiv : the preprint server for health sciences · 2025
    Article
  17. Article
  18. Article
  19. Article
  20. 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

3 authors.

Teresa de Los Reyes CorralesInstituto Cajal (CSIC), Av. Doctor Arce 37, 28002 Madrid, Spain.
María Losada-PérezInstituto Cajal (CSIC), Av. Doctor Arce 37, 28002 Madrid, Spain.ORCID 0000-0002-6717-7762
Sergio Casas-TintóInstituto Cajal (CSIC), Av. Doctor Arce 37, 28002 Madrid, Spain.ORCID 0000-0002-9589-9981

Funding

CSIC LINKA 20268Ministerio de Ciencia e Innovación PID2019-110116GB-100
6 · The paper itself

Abstract

The c-Jun N-terminal kinase (JNK) signalling pathway is a conserved response to a wide range of internal and external cellular stress signals. Beside the stress response, the JNK pathway is involved in a series of vital regulatory mechanisms during development and adulthood that are critical to maintain tissue homeostasis. These mechanisms include the regulation of apoptosis, growth, proliferation, differentiation, migration and invasion. The JNK pathway has a diverse functionality and cell-tissue specificity, and has emerged as a key player in regeneration, tumorigenesis and other pathologies. The JNK pathway is highly active in the central nervous system (CNS), and plays a central role when cells need to cope with pathophysiological insults during development and adulthood. Here, we review the implications of the JNK pathway in pathologies of the CNS. More specifically, we discuss some newly identified examples and mechanisms of JNK-driven tumor progression in glioblastoma, regeneration/repair after an injury, neurodegeneration and neuronal cell death. All these new discoveries support the central role of JNK in CNS pathologies and reinforce the idea of JNK as potential target to reduce their detrimental effects.

Indexed as

Disease SusceptibilityMAP Kinase Signaling SystemAnimalsBiomarkersCentral Nervous SystemCentral Nervous System DiseasesHumansJNK Mitogen-Activated Protein KinasesBiomarkersJNK Mitogen-Activated Protein Kinasescell signallingCNS injuriesglioblastomaMAP kinaseneurodegenerative disorders

Identifiers

PMID33918666
PMCPMC8070500

What OpenQuestion holds

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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.