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Multiplex Screening for Interacting Compounds in Paediatric Acute Myeloid Leukaemia

Paediatric acute myeloid leukaemia (AML) is a heterogeneous disease characterised by the malignant transformation of myeloid precursor cells with impaired differentiation. Standard therapy for paediatric AML has remained largely unchanged for over four decades and, combined with inadequate understan...

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Autores principales: Cairns, Lauren V., Lappin, Katrina M., Mutch, Alexander, Ali, Ahlam, Matchett, Kyle B., Mills, Ken I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8468645/
https://www.ncbi.nlm.nih.gov/pubmed/34576326
http://dx.doi.org/10.3390/ijms221810163
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author Cairns, Lauren V.
Lappin, Katrina M.
Mutch, Alexander
Ali, Ahlam
Matchett, Kyle B.
Mills, Ken I.
author_facet Cairns, Lauren V.
Lappin, Katrina M.
Mutch, Alexander
Ali, Ahlam
Matchett, Kyle B.
Mills, Ken I.
author_sort Cairns, Lauren V.
collection PubMed
description Paediatric acute myeloid leukaemia (AML) is a heterogeneous disease characterised by the malignant transformation of myeloid precursor cells with impaired differentiation. Standard therapy for paediatric AML has remained largely unchanged for over four decades and, combined with inadequate understanding of the biology of paediatric AML, has limited the progress of targeted therapies in this cohort. In recent years, the search for novel targets for the treatment of paediatric AML has accelerated in parallel with advanced genomic technologies which explore the mutational and transcriptional landscape of this disease. Exploiting the large combinatorial space of existing drugs provides an untapped resource for the identification of potential combination therapies for the treatment of paediatric AML. We have previously designed a multiplex screening strategy known as Multiplex Screening for Interacting Compounds in AML (MuSICAL); using an algorithm designed in-house, we screened all pairings of 384 FDA-approved compounds in less than 4000 wells by pooling drugs into 10 compounds per well. This approach maximised the probability of identifying new compound combinations with therapeutic potential while minimising cost, replication and redundancy. This screening strategy identified the triple combination of glimepiride, a sulfonylurea; pancuronium dibromide, a neuromuscular blocking agent; and vinblastine sulfate, a vinca alkaloid, as a potential therapy for paediatric AML. We envision that this approach can be used for a variety of disease-relevant screens allowing the efficient repurposing of drugs that can be rapidly moved into the clinic.
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spelling pubmed-84686452021-09-27 Multiplex Screening for Interacting Compounds in Paediatric Acute Myeloid Leukaemia Cairns, Lauren V. Lappin, Katrina M. Mutch, Alexander Ali, Ahlam Matchett, Kyle B. Mills, Ken I. Int J Mol Sci Article Paediatric acute myeloid leukaemia (AML) is a heterogeneous disease characterised by the malignant transformation of myeloid precursor cells with impaired differentiation. Standard therapy for paediatric AML has remained largely unchanged for over four decades and, combined with inadequate understanding of the biology of paediatric AML, has limited the progress of targeted therapies in this cohort. In recent years, the search for novel targets for the treatment of paediatric AML has accelerated in parallel with advanced genomic technologies which explore the mutational and transcriptional landscape of this disease. Exploiting the large combinatorial space of existing drugs provides an untapped resource for the identification of potential combination therapies for the treatment of paediatric AML. We have previously designed a multiplex screening strategy known as Multiplex Screening for Interacting Compounds in AML (MuSICAL); using an algorithm designed in-house, we screened all pairings of 384 FDA-approved compounds in less than 4000 wells by pooling drugs into 10 compounds per well. This approach maximised the probability of identifying new compound combinations with therapeutic potential while minimising cost, replication and redundancy. This screening strategy identified the triple combination of glimepiride, a sulfonylurea; pancuronium dibromide, a neuromuscular blocking agent; and vinblastine sulfate, a vinca alkaloid, as a potential therapy for paediatric AML. We envision that this approach can be used for a variety of disease-relevant screens allowing the efficient repurposing of drugs that can be rapidly moved into the clinic. MDPI 2021-09-21 /pmc/articles/PMC8468645/ /pubmed/34576326 http://dx.doi.org/10.3390/ijms221810163 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Cairns, Lauren V.
Lappin, Katrina M.
Mutch, Alexander
Ali, Ahlam
Matchett, Kyle B.
Mills, Ken I.
Multiplex Screening for Interacting Compounds in Paediatric Acute Myeloid Leukaemia
title Multiplex Screening for Interacting Compounds in Paediatric Acute Myeloid Leukaemia
title_full Multiplex Screening for Interacting Compounds in Paediatric Acute Myeloid Leukaemia
title_fullStr Multiplex Screening for Interacting Compounds in Paediatric Acute Myeloid Leukaemia
title_full_unstemmed Multiplex Screening for Interacting Compounds in Paediatric Acute Myeloid Leukaemia
title_short Multiplex Screening for Interacting Compounds in Paediatric Acute Myeloid Leukaemia
title_sort multiplex screening for interacting compounds in paediatric acute myeloid leukaemia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8468645/
https://www.ncbi.nlm.nih.gov/pubmed/34576326
http://dx.doi.org/10.3390/ijms221810163
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