Evidence map›Paper›PMID 28502042›Full record

ReviewMolecular neurobiology2018

Tale of the Good and the Bad Cdk5: Remodeling of the Actin Cytoskeleton in the Brain.

Kavita Shah, Sandra Rossie

Abstract readReview
In one paragraph

Review in Molecular neurobiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed
4.5field-weighted citation impact, top 4% 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

62 citing papers in PubMed, 101 citations in OpenAlex.

  1. The Recycling Endosomal (NaActa physiologica (Oxford, England) · 2026
    Article
  2. Article
  3. Article
  4. A patent review of cyclin-dependent kinase 5 (CDK5) inhibitors (1999-2025).Frontiers in bioengineering and biotechnology · 2026
    Review
  5. Review
  6. Article
  7. Epigenetic Effects and Potential Contributions of mAnimals : an open access journal from MDPI · 2025
    Article
  8. Article
  9. Article
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  11. Article
  12. Article
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  15. Article
  16. Case report: AFrontiers in neuroscience · 2024
    Article
  17. Review
  18. Article
  19. Article
  20. Article

2 more citing papers are in PubMed but not listed here.

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

2 authors at 1 institution in 1 country.

Kavita ShahDepartment of Chemistry and Purdue University Center of Cancer Research, Purdue University, 560 Oval Drive, West Lafayette, IN, 47907, USA. shah23@purdue.edu.ORCID http://orcid.org/0000-0002-0451-1305
Sandra RossieDepartment of Biochemistry, Purdue University, West Lafayette, IN, 47907, USA.
Purdue University West Lafayette · US

Funding

Exploring FOXO Signaling in Promoting Neurodegeneration in ADR21AG047447 · NIA · PURDUE UNIVERSITY · PI SHAH, KAVITA · 2014 to 2015
$435k
National Institute on Aging NIAR21AG 47447NIA NIH HHS R21 AG047447
6 · The paper itself

Abstract

Cdk5 kinase, a cyclin-dependent kinase family member, is a key regulator of cytoskeletal remodeling in the brain. Cdk5 is essential for brain development during embryogenesis. After birth, it is essential for numerous neuronal processes such as learning and memory formation, drug addiction, pain signaling, and long-term behavior changes, all of which rely on rapid alterations in the cytoskeleton. Cdk5 activity is deregulated in various brain disorders including Alzheimer's disease, Parkinson's disease, amyotrophic lateral sclerosis, and ischemic stroke, resulting in profound remodeling of the neuronal cytoskeleton, loss of synapses, and ultimately neurodegeneration. This review focuses on the "good and bad" Cdk5 in the brain and its pleiotropic contribution in regulating neuronal actin cytoskeletal remodeling. A vast majority of physiological and pathological Cdk5 substrates are associated with the actin cytoskeleton. Thus, our special emphasis is on the numerous Cdk5 substrates identified in the past two decades such as ephexin1, p27, Mst3, CaMKv, kalirin-7, RasGRF2, Pak1, WAVE1, neurabin-1, TrkB, 5-HT6R, talin, drebrin, synapsin I, synapsin III, CRMP1, GKAP, SPAR, PSD-95, and LRRK2. These substrates have unraveled the molecular mechanisms by which Cdk5 plays divergent roles in regulating neuronal actin cytoskeletal dynamics both in healthy and diseased states.

Indexed as

Actin CytoskeletonAnimalsBrainCyclin-Dependent Kinase 5HumansModels, BiologicalNeuronsPresynaptic TerminalsCyclin-Dependent Kinase 55-HT6RActinAlzheimer’s diseaseAxonal growthCaMKvCdkCdk5CRMP1CyclinsDendritic spinesDrebrinDrug addictionEphexin1GKAPKalirin-7Learning and memoryLRRK2MicrotubulesMst3Neurabin-1NeurodegenerationNeuronal cytoskeletonNeuronal migrationNeurotransmittersp25p35Pak1Parkinson’s diseasePSD-95RasGRF2RemodelingSPARSynapsin ISynapsin IIISynaptic plasticitySynaptogenesisTalinTrkBWAVE1β-Amyloid

Identifiers

PMID28502042
PMCPMC6370010
OpenAlexW2612194469

What OpenQuestion holds

Textmetadata
LicenceTDM
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.