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RUNX1 Dosage in Development and Cancer

The transcription factor RUNX1 first came to prominence due to its involvement in the t(8;21) translocation in acute myeloid leukemia (AML). Since this discovery, RUNX1 has been shown to play important roles not only in leukemia but also in the ontogeny of the normal hematopoietic system. Although i...

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Autores principales: Lie-a-ling, Michael, Mevel, Renaud, Patel, Rahima, Blyth, Karen, Baena, Esther, Kouskoff, Valerie, Lacaud, Georges
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society for Molecular and Cellular Biology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7057845/
https://www.ncbi.nlm.nih.gov/pubmed/31991535
http://dx.doi.org/10.14348/molcells.2019.0301
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author Lie-a-ling, Michael
Mevel, Renaud
Patel, Rahima
Blyth, Karen
Baena, Esther
Kouskoff, Valerie
Lacaud, Georges
author_facet Lie-a-ling, Michael
Mevel, Renaud
Patel, Rahima
Blyth, Karen
Baena, Esther
Kouskoff, Valerie
Lacaud, Georges
author_sort Lie-a-ling, Michael
collection PubMed
description The transcription factor RUNX1 first came to prominence due to its involvement in the t(8;21) translocation in acute myeloid leukemia (AML). Since this discovery, RUNX1 has been shown to play important roles not only in leukemia but also in the ontogeny of the normal hematopoietic system. Although it is currently still challenging to fully assess the different parameters regulating RUNX1 dosage, it has become clear that the dose of RUNX1 can greatly affect both leukemia and normal hematopoietic development. It is also becoming evident that varying levels of RUNX1 expression can be used as markers of tumor progression not only in the hematopoietic system, but also in non-hematopoietic cancers. Here, we provide an overview of the current knowledge of the effects of RUNX1 dosage in normal development of both hematopoietic and epithelial tissues and their associated cancers.
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spelling pubmed-70578452020-03-12 RUNX1 Dosage in Development and Cancer Lie-a-ling, Michael Mevel, Renaud Patel, Rahima Blyth, Karen Baena, Esther Kouskoff, Valerie Lacaud, Georges Mol Cells Minireview The transcription factor RUNX1 first came to prominence due to its involvement in the t(8;21) translocation in acute myeloid leukemia (AML). Since this discovery, RUNX1 has been shown to play important roles not only in leukemia but also in the ontogeny of the normal hematopoietic system. Although it is currently still challenging to fully assess the different parameters regulating RUNX1 dosage, it has become clear that the dose of RUNX1 can greatly affect both leukemia and normal hematopoietic development. It is also becoming evident that varying levels of RUNX1 expression can be used as markers of tumor progression not only in the hematopoietic system, but also in non-hematopoietic cancers. Here, we provide an overview of the current knowledge of the effects of RUNX1 dosage in normal development of both hematopoietic and epithelial tissues and their associated cancers. Korean Society for Molecular and Cellular Biology 2020-02-29 2020-01-24 /pmc/articles/PMC7057845/ /pubmed/31991535 http://dx.doi.org/10.14348/molcells.2019.0301 Text en © The Korean Society for Molecular and Cellular Biology. All rights reserved. This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Minireview
Lie-a-ling, Michael
Mevel, Renaud
Patel, Rahima
Blyth, Karen
Baena, Esther
Kouskoff, Valerie
Lacaud, Georges
RUNX1 Dosage in Development and Cancer
title RUNX1 Dosage in Development and Cancer
title_full RUNX1 Dosage in Development and Cancer
title_fullStr RUNX1 Dosage in Development and Cancer
title_full_unstemmed RUNX1 Dosage in Development and Cancer
title_short RUNX1 Dosage in Development and Cancer
title_sort runx1 dosage in development and cancer
topic Minireview
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7057845/
https://www.ncbi.nlm.nih.gov/pubmed/31991535
http://dx.doi.org/10.14348/molcells.2019.0301
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