Literature DB >> 33572709

Mechanisms and Therapeutic Implications of GSK-3 in Treating Neurodegeneration.

Ido Rippin1, Hagit Eldar-Finkelman1.   

Abstract

Neurodegenerative disorders are spreading worldwide and are one of the greatest threats to public health. There is currently no adequate therapy for these disorders, and therefore there is an urgent need to accelerate the discovery and development of effective treatments. Although neurodegenerative disorders are broad ranging and highly complex, they may share overlapping mechanisms, and thus potentially manifest common targets for therapeutic interventions. Glycogen synthase kinase-3 (GSK-3) is now acknowledged to be a central player in regulating mood behavior, cognitive functions, and neuron viability. Indeed, many targets controlled by GSK-3 are critically involved in progressing neuron deterioration and disease pathogenesis. In this review, we focus on three pathways that represent prominent mechanisms linking GSK-3 with neurodegenerative disorders: cytoskeleton organization, the mammalian target of rapamycin (mTOR)/autophagy axis, and mitochondria. We also consider the challenges and opportunities in the development of GSK-3 inhibitors for treating neurodegeneration.

Entities:  

Keywords:  GSK-3; GSK-3 inhibitors; autophagy; lysosome; mTOR; microtubules; mitochondria; neurodegeneration

Year:  2021        PMID: 33572709      PMCID: PMC7911291          DOI: 10.3390/cells10020262

Source DB:  PubMed          Journal:  Cells        ISSN: 2073-4409            Impact factor:   6.600


  232 in total

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3.  Underlying mechanisms of recombinant adeno-associated virus-mediated bicaudal C homolog 1 overexpression in the medial prefrontal cortex of mice with induced depressive-like behaviors.

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4.  Binding of the adenomatous polyposis coli protein to microtubules increases microtubule stability and is regulated by GSK3 beta phosphorylation.

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Journal:  Curr Biol       Date:  2001-01-09       Impact factor: 10.834

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Journal:  Nature       Date:  2000-07-06       Impact factor: 49.962

7.  Convergent evidence for impaired AKT1-GSK3beta signaling in schizophrenia.

Authors:  Effat S Emamian; Diana Hall; Morris J Birnbaum; Maria Karayiorgou; Joseph A Gogos
Journal:  Nat Genet       Date:  2004-01-25       Impact factor: 38.330

Review 8.  GSK-3β, a pivotal kinase in Alzheimer disease.

Authors:  María Llorens-Martín; Jerónimo Jurado; Félix Hernández; Jesús Avila
Journal:  Front Mol Neurosci       Date:  2014-05-21       Impact factor: 5.639

9.  Neurological characterization of mice deficient in GSK3α highlight pleiotropic physiological functions in cognition and pathological activity as Tau kinase.

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Journal:  Mol Brain       Date:  2013-05-25       Impact factor: 4.041

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  6 in total

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2.  GSK-3β Inhibition in Birds Affects Social Behavior and Increases Motor Activity.

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3.  Prospects in GSK-3 Signaling: From Cellular Regulation to Disease Therapy.

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Journal:  Cells       Date:  2022-05-12       Impact factor: 7.666

Review 4.  Glycogen Synthase Kinase-3 Inhibitors: Preclinical and Clinical Focus on CNS-A Decade Onward.

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Journal:  Front Mol Neurosci       Date:  2022-01-21       Impact factor: 5.639

5.  Identification of Novel GSK-3β Hits Using Competitive Biophysical Assays.

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Review 6.  GSK-3 and Tau: A Key Duet in Alzheimer's Disease.

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Journal:  Cells       Date:  2021-03-24       Impact factor: 6.600

  6 in total

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