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CK2—An Emerging Target for Neurological and Psychiatric Disorders

Protein kinase CK2 has received a surge of attention in recent years due to the evidence of its overexpression in a variety of solid tumors and multiple myelomas as well as its participation in cell survival pathways. CK2 is also upregulated in the most prevalent and aggressive cancer of brain tissu...

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Autores principales: Castello, Julia, Ragnauth, Andre, Friedman, Eitan, Rebholz, Heike
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5374411/
https://www.ncbi.nlm.nih.gov/pubmed/28067771
http://dx.doi.org/10.3390/ph10010007
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author Castello, Julia
Ragnauth, Andre
Friedman, Eitan
Rebholz, Heike
author_facet Castello, Julia
Ragnauth, Andre
Friedman, Eitan
Rebholz, Heike
author_sort Castello, Julia
collection PubMed
description Protein kinase CK2 has received a surge of attention in recent years due to the evidence of its overexpression in a variety of solid tumors and multiple myelomas as well as its participation in cell survival pathways. CK2 is also upregulated in the most prevalent and aggressive cancer of brain tissue, glioblastoma multiforme, and in preclinical models, pharmacological inhibition of the kinase has proven successful in reducing tumor size and animal mortality. CK2 is highly expressed in the mammalian brain and has many bona fide substrates that are crucial in neuronal or glial homeostasis and signaling processes across synapses. Full and conditional CK2 knockout mice have further elucidated the importance of CK2 in brain development, neuronal activity, and behavior. This review will discuss recent advances in the field that point to CK2 as a regulator of neuronal functions and as a potential novel target to treat neurological and psychiatric disorders.
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spelling pubmed-53744112017-04-10 CK2—An Emerging Target for Neurological and Psychiatric Disorders Castello, Julia Ragnauth, Andre Friedman, Eitan Rebholz, Heike Pharmaceuticals (Basel) Review Protein kinase CK2 has received a surge of attention in recent years due to the evidence of its overexpression in a variety of solid tumors and multiple myelomas as well as its participation in cell survival pathways. CK2 is also upregulated in the most prevalent and aggressive cancer of brain tissue, glioblastoma multiforme, and in preclinical models, pharmacological inhibition of the kinase has proven successful in reducing tumor size and animal mortality. CK2 is highly expressed in the mammalian brain and has many bona fide substrates that are crucial in neuronal or glial homeostasis and signaling processes across synapses. Full and conditional CK2 knockout mice have further elucidated the importance of CK2 in brain development, neuronal activity, and behavior. This review will discuss recent advances in the field that point to CK2 as a regulator of neuronal functions and as a potential novel target to treat neurological and psychiatric disorders. MDPI 2017-01-05 /pmc/articles/PMC5374411/ /pubmed/28067771 http://dx.doi.org/10.3390/ph10010007 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Castello, Julia
Ragnauth, Andre
Friedman, Eitan
Rebholz, Heike
CK2—An Emerging Target for Neurological and Psychiatric Disorders
title CK2—An Emerging Target for Neurological and Psychiatric Disorders
title_full CK2—An Emerging Target for Neurological and Psychiatric Disorders
title_fullStr CK2—An Emerging Target for Neurological and Psychiatric Disorders
title_full_unstemmed CK2—An Emerging Target for Neurological and Psychiatric Disorders
title_short CK2—An Emerging Target for Neurological and Psychiatric Disorders
title_sort ck2—an emerging target for neurological and psychiatric disorders
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5374411/
https://www.ncbi.nlm.nih.gov/pubmed/28067771
http://dx.doi.org/10.3390/ph10010007
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