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Biological functions of casein kinase 1 isoforms and putative roles in tumorigenesis

Isoforms of the casein kinase 1 (CK1) family have been shown to phosphorylate key regulatory molecules involved in cell cycle, transcription and translation, the structure of the cytoskeleton, cell-cell adhesion and receptor-coupled signal transduction. They regulate key signaling pathways known to...

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Detalles Bibliográficos
Autores principales: Schittek, Birgit, Sinnberg, Tobias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4201705/
https://www.ncbi.nlm.nih.gov/pubmed/25306547
http://dx.doi.org/10.1186/1476-4598-13-231
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author Schittek, Birgit
Sinnberg, Tobias
author_facet Schittek, Birgit
Sinnberg, Tobias
author_sort Schittek, Birgit
collection PubMed
description Isoforms of the casein kinase 1 (CK1) family have been shown to phosphorylate key regulatory molecules involved in cell cycle, transcription and translation, the structure of the cytoskeleton, cell-cell adhesion and receptor-coupled signal transduction. They regulate key signaling pathways known to be critically involved in tumor progression. Recent results point to an altered expression or activity of different CK1 isoforms in tumor cells. This review summarizes the expression and biological function of CK1 family members in normal and malignant cells and the evidence obtained so far about their role in tumorigenesis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1476-4598-13-231) contains supplementary material, which is available to authorized users.
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spelling pubmed-42017052014-10-19 Biological functions of casein kinase 1 isoforms and putative roles in tumorigenesis Schittek, Birgit Sinnberg, Tobias Mol Cancer Review Isoforms of the casein kinase 1 (CK1) family have been shown to phosphorylate key regulatory molecules involved in cell cycle, transcription and translation, the structure of the cytoskeleton, cell-cell adhesion and receptor-coupled signal transduction. They regulate key signaling pathways known to be critically involved in tumor progression. Recent results point to an altered expression or activity of different CK1 isoforms in tumor cells. This review summarizes the expression and biological function of CK1 family members in normal and malignant cells and the evidence obtained so far about their role in tumorigenesis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1476-4598-13-231) contains supplementary material, which is available to authorized users. BioMed Central 2014-10-11 /pmc/articles/PMC4201705/ /pubmed/25306547 http://dx.doi.org/10.1186/1476-4598-13-231 Text en © Schittek and Sinnberg; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Schittek, Birgit
Sinnberg, Tobias
Biological functions of casein kinase 1 isoforms and putative roles in tumorigenesis
title Biological functions of casein kinase 1 isoforms and putative roles in tumorigenesis
title_full Biological functions of casein kinase 1 isoforms and putative roles in tumorigenesis
title_fullStr Biological functions of casein kinase 1 isoforms and putative roles in tumorigenesis
title_full_unstemmed Biological functions of casein kinase 1 isoforms and putative roles in tumorigenesis
title_short Biological functions of casein kinase 1 isoforms and putative roles in tumorigenesis
title_sort biological functions of casein kinase 1 isoforms and putative roles in tumorigenesis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4201705/
https://www.ncbi.nlm.nih.gov/pubmed/25306547
http://dx.doi.org/10.1186/1476-4598-13-231
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