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Targeting Apoptotic Pathways in Acute Myeloid Leukaemia

Acute Myeloid Leukaemia is a devastating disease that continues to have a poor outcome for the majority of patients. In recent years, however, a number of drugs have received FDA approval, following on from successful clinical trial results. This parallels the characterization of the molecular lands...

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Autores principales: Sillar, Jonathan R., Enjeti, Anoop K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6895902/
https://www.ncbi.nlm.nih.gov/pubmed/31717784
http://dx.doi.org/10.3390/cancers11111660
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author Sillar, Jonathan R.
Enjeti, Anoop K.
author_facet Sillar, Jonathan R.
Enjeti, Anoop K.
author_sort Sillar, Jonathan R.
collection PubMed
description Acute Myeloid Leukaemia is a devastating disease that continues to have a poor outcome for the majority of patients. In recent years, however, a number of drugs have received FDA approval, following on from successful clinical trial results. This parallels the characterization of the molecular landscape of Acute Myeloid Leukaemia (AML) over the last decade, which has led to the development of drugs targeting newly identified recurring mutations. In addition, basic biological research into the pathobiology of AML has identified aberrant programmed cell death pathways in AML. Following on from successful outcomes in lymphoid malignancies, drugs targeting the B Cell Lymphoma 2 (BCL-2) family of anti-apoptotic proteins have been explored in AML. In this review, we will outline the preclinical and clinical work to date supporting the role of drugs targeting BCL-2, with Venetoclax being the most advanced to date. We will also highlight rationale combinations using Venetoclax, ongoing clinical trials and biomarkers of response identified from the early phase clinical trials performed.
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spelling pubmed-68959022019-12-24 Targeting Apoptotic Pathways in Acute Myeloid Leukaemia Sillar, Jonathan R. Enjeti, Anoop K. Cancers (Basel) Review Acute Myeloid Leukaemia is a devastating disease that continues to have a poor outcome for the majority of patients. In recent years, however, a number of drugs have received FDA approval, following on from successful clinical trial results. This parallels the characterization of the molecular landscape of Acute Myeloid Leukaemia (AML) over the last decade, which has led to the development of drugs targeting newly identified recurring mutations. In addition, basic biological research into the pathobiology of AML has identified aberrant programmed cell death pathways in AML. Following on from successful outcomes in lymphoid malignancies, drugs targeting the B Cell Lymphoma 2 (BCL-2) family of anti-apoptotic proteins have been explored in AML. In this review, we will outline the preclinical and clinical work to date supporting the role of drugs targeting BCL-2, with Venetoclax being the most advanced to date. We will also highlight rationale combinations using Venetoclax, ongoing clinical trials and biomarkers of response identified from the early phase clinical trials performed. MDPI 2019-10-26 /pmc/articles/PMC6895902/ /pubmed/31717784 http://dx.doi.org/10.3390/cancers11111660 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
Sillar, Jonathan R.
Enjeti, Anoop K.
Targeting Apoptotic Pathways in Acute Myeloid Leukaemia
title Targeting Apoptotic Pathways in Acute Myeloid Leukaemia
title_full Targeting Apoptotic Pathways in Acute Myeloid Leukaemia
title_fullStr Targeting Apoptotic Pathways in Acute Myeloid Leukaemia
title_full_unstemmed Targeting Apoptotic Pathways in Acute Myeloid Leukaemia
title_short Targeting Apoptotic Pathways in Acute Myeloid Leukaemia
title_sort targeting apoptotic pathways in acute myeloid leukaemia
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6895902/
https://www.ncbi.nlm.nih.gov/pubmed/31717784
http://dx.doi.org/10.3390/cancers11111660
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