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The Transcriptional Roles of ALK Fusion Proteins in Tumorigenesis

Anaplastic lymphoma kinase (ALK) is a tyrosine kinase involved in neuronal and gut development. Initially discovered in T cell lymphoma, ALK is frequently affected in diverse cancers by oncogenic translocations. These translocations involve different fusion partners that facilitate multimerisation a...

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Autores principales: Ducray, Stephen P., Natarajan, Karthikraj, Garland, Gavin D., Turner, Suzanne D., Egger, Gerda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6721376/
https://www.ncbi.nlm.nih.gov/pubmed/31366041
http://dx.doi.org/10.3390/cancers11081074
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author Ducray, Stephen P.
Natarajan, Karthikraj
Garland, Gavin D.
Turner, Suzanne D.
Egger, Gerda
author_facet Ducray, Stephen P.
Natarajan, Karthikraj
Garland, Gavin D.
Turner, Suzanne D.
Egger, Gerda
author_sort Ducray, Stephen P.
collection PubMed
description Anaplastic lymphoma kinase (ALK) is a tyrosine kinase involved in neuronal and gut development. Initially discovered in T cell lymphoma, ALK is frequently affected in diverse cancers by oncogenic translocations. These translocations involve different fusion partners that facilitate multimerisation and autophosphorylation of ALK, resulting in a constitutively active tyrosine kinase with oncogenic potential. ALK fusion proteins are involved in diverse cellular signalling pathways, such as Ras/extracellular signal-regulated kinase (ERK), phosphatidylinositol 3-kinase (PI3K)/Akt and Janus protein tyrosine kinase (JAK)/STAT. Furthermore, ALK is implicated in epigenetic regulation, including DNA methylation and miRNA expression, and an interaction with nuclear proteins has been described. Through these mechanisms, ALK fusion proteins enable a transcriptional programme that drives the pathogenesis of a range of ALK-related malignancies.
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spelling pubmed-67213762019-09-10 The Transcriptional Roles of ALK Fusion Proteins in Tumorigenesis Ducray, Stephen P. Natarajan, Karthikraj Garland, Gavin D. Turner, Suzanne D. Egger, Gerda Cancers (Basel) Review Anaplastic lymphoma kinase (ALK) is a tyrosine kinase involved in neuronal and gut development. Initially discovered in T cell lymphoma, ALK is frequently affected in diverse cancers by oncogenic translocations. These translocations involve different fusion partners that facilitate multimerisation and autophosphorylation of ALK, resulting in a constitutively active tyrosine kinase with oncogenic potential. ALK fusion proteins are involved in diverse cellular signalling pathways, such as Ras/extracellular signal-regulated kinase (ERK), phosphatidylinositol 3-kinase (PI3K)/Akt and Janus protein tyrosine kinase (JAK)/STAT. Furthermore, ALK is implicated in epigenetic regulation, including DNA methylation and miRNA expression, and an interaction with nuclear proteins has been described. Through these mechanisms, ALK fusion proteins enable a transcriptional programme that drives the pathogenesis of a range of ALK-related malignancies. MDPI 2019-07-30 /pmc/articles/PMC6721376/ /pubmed/31366041 http://dx.doi.org/10.3390/cancers11081074 Text en © 2019 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
Ducray, Stephen P.
Natarajan, Karthikraj
Garland, Gavin D.
Turner, Suzanne D.
Egger, Gerda
The Transcriptional Roles of ALK Fusion Proteins in Tumorigenesis
title The Transcriptional Roles of ALK Fusion Proteins in Tumorigenesis
title_full The Transcriptional Roles of ALK Fusion Proteins in Tumorigenesis
title_fullStr The Transcriptional Roles of ALK Fusion Proteins in Tumorigenesis
title_full_unstemmed The Transcriptional Roles of ALK Fusion Proteins in Tumorigenesis
title_short The Transcriptional Roles of ALK Fusion Proteins in Tumorigenesis
title_sort transcriptional roles of alk fusion proteins in tumorigenesis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6721376/
https://www.ncbi.nlm.nih.gov/pubmed/31366041
http://dx.doi.org/10.3390/cancers11081074
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