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Retinoic Acid Receptors in Acute Myeloid Leukemia Therapy
Retinoic acid (RA) signaling pathways regulate fundamental biological processes, such as cell proliferation, development, differentiation, and apoptosis. Retinoid receptors (RARs and RXRs) are ligand-dependent transcription factors. All-trans retinoic acid (ATRA) is the principal endogenous ligand f...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6966485/ https://www.ncbi.nlm.nih.gov/pubmed/31805753 http://dx.doi.org/10.3390/cancers11121915 |
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author | di Martino, Orsola Welch, John S. |
author_facet | di Martino, Orsola Welch, John S. |
author_sort | di Martino, Orsola |
collection | PubMed |
description | Retinoic acid (RA) signaling pathways regulate fundamental biological processes, such as cell proliferation, development, differentiation, and apoptosis. Retinoid receptors (RARs and RXRs) are ligand-dependent transcription factors. All-trans retinoic acid (ATRA) is the principal endogenous ligand for the retinoic acid receptor alpha (RARA) and is produced by the enzymatic oxidation of dietary vitamin A, whose deficiency is associated with several pathological conditions. Differentiation therapy using ATRA revolutionized the outcome of acute promyelocytic leukemia (APL), although attempts to replicate these results in other cancer types have been met with more modest results. A better knowledge of RA signaling in different leukemia contexts is required to improve initial designs. Here, we will review the RA signaling pathway in normal and malignant hematopoiesis, and will discuss the advantages and the limitations related to retinoid therapy in acute myeloid leukemia. |
format | Online Article Text |
id | pubmed-6966485 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-69664852020-01-27 Retinoic Acid Receptors in Acute Myeloid Leukemia Therapy di Martino, Orsola Welch, John S. Cancers (Basel) Review Retinoic acid (RA) signaling pathways regulate fundamental biological processes, such as cell proliferation, development, differentiation, and apoptosis. Retinoid receptors (RARs and RXRs) are ligand-dependent transcription factors. All-trans retinoic acid (ATRA) is the principal endogenous ligand for the retinoic acid receptor alpha (RARA) and is produced by the enzymatic oxidation of dietary vitamin A, whose deficiency is associated with several pathological conditions. Differentiation therapy using ATRA revolutionized the outcome of acute promyelocytic leukemia (APL), although attempts to replicate these results in other cancer types have been met with more modest results. A better knowledge of RA signaling in different leukemia contexts is required to improve initial designs. Here, we will review the RA signaling pathway in normal and malignant hematopoiesis, and will discuss the advantages and the limitations related to retinoid therapy in acute myeloid leukemia. MDPI 2019-12-01 /pmc/articles/PMC6966485/ /pubmed/31805753 http://dx.doi.org/10.3390/cancers11121915 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 di Martino, Orsola Welch, John S. Retinoic Acid Receptors in Acute Myeloid Leukemia Therapy |
title | Retinoic Acid Receptors in Acute Myeloid Leukemia Therapy |
title_full | Retinoic Acid Receptors in Acute Myeloid Leukemia Therapy |
title_fullStr | Retinoic Acid Receptors in Acute Myeloid Leukemia Therapy |
title_full_unstemmed | Retinoic Acid Receptors in Acute Myeloid Leukemia Therapy |
title_short | Retinoic Acid Receptors in Acute Myeloid Leukemia Therapy |
title_sort | retinoic acid receptors in acute myeloid leukemia therapy |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6966485/ https://www.ncbi.nlm.nih.gov/pubmed/31805753 http://dx.doi.org/10.3390/cancers11121915 |
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