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Targeting apoptosis in acute myeloid leukaemia
Acute myeloid leukaemia (AML) is a molecularly and clinically heterogeneous disease, and its incidence is increasing as the populations in Western countries age. Despite major advances in understanding the genetic landscape of AML and its impact on the biology of the disease, standard therapy has no...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5674101/ https://www.ncbi.nlm.nih.gov/pubmed/29017180 http://dx.doi.org/10.1038/bjc.2017.281 |
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author | Cassier, Philippe A Castets, Marie Belhabri, Amine Vey, Norbert |
author_facet | Cassier, Philippe A Castets, Marie Belhabri, Amine Vey, Norbert |
author_sort | Cassier, Philippe A |
collection | PubMed |
description | Acute myeloid leukaemia (AML) is a molecularly and clinically heterogeneous disease, and its incidence is increasing as the populations in Western countries age. Despite major advances in understanding the genetic landscape of AML and its impact on the biology of the disease, standard therapy has not changed significantly in the last three decades. Allogeneic haematopoietic stem cell transplantation remains the best chance for cure, but can only be offered to a minority of younger fit patients. Molecularly targeted drugs aiming at restoring apoptosis in leukaemic cells have shown encouraging activity in early clinical trials and some of these drugs are currently being evaluated in randomised controlled trials. In this review, we discuss the current development of drugs designed to trigger cell death in AML. |
format | Online Article Text |
id | pubmed-5674101 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-56741012017-11-08 Targeting apoptosis in acute myeloid leukaemia Cassier, Philippe A Castets, Marie Belhabri, Amine Vey, Norbert Br J Cancer Review Acute myeloid leukaemia (AML) is a molecularly and clinically heterogeneous disease, and its incidence is increasing as the populations in Western countries age. Despite major advances in understanding the genetic landscape of AML and its impact on the biology of the disease, standard therapy has not changed significantly in the last three decades. Allogeneic haematopoietic stem cell transplantation remains the best chance for cure, but can only be offered to a minority of younger fit patients. Molecularly targeted drugs aiming at restoring apoptosis in leukaemic cells have shown encouraging activity in early clinical trials and some of these drugs are currently being evaluated in randomised controlled trials. In this review, we discuss the current development of drugs designed to trigger cell death in AML. Nature Publishing Group 2017-10-10 2017-08-24 /pmc/articles/PMC5674101/ /pubmed/29017180 http://dx.doi.org/10.1038/bjc.2017.281 Text en Copyright © 2017 The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Review Cassier, Philippe A Castets, Marie Belhabri, Amine Vey, Norbert Targeting apoptosis in acute myeloid leukaemia |
title | Targeting apoptosis in acute myeloid leukaemia |
title_full | Targeting apoptosis in acute myeloid leukaemia |
title_fullStr | Targeting apoptosis in acute myeloid leukaemia |
title_full_unstemmed | Targeting apoptosis in acute myeloid leukaemia |
title_short | Targeting apoptosis in acute myeloid leukaemia |
title_sort | targeting apoptosis in acute myeloid leukaemia |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5674101/ https://www.ncbi.nlm.nih.gov/pubmed/29017180 http://dx.doi.org/10.1038/bjc.2017.281 |
work_keys_str_mv | AT cassierphilippea targetingapoptosisinacutemyeloidleukaemia AT castetsmarie targetingapoptosisinacutemyeloidleukaemia AT belhabriamine targetingapoptosisinacutemyeloidleukaemia AT veynorbert targetingapoptosisinacutemyeloidleukaemia |