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儿科急性髓细胞白血病相互作用化合物的多重筛选。

Multiplex Screening for Interacting Compounds in Paediatric Acute Myeloid Leukaemia.

机构信息

Patrick G. Johnston Centre for Cancer Research, Queen's University Belfast, 97 Lisburn Road, Belfast BT9 7AE, UK.

Northern Ireland Centre for Stratified Medicine, School of Biomedical Sciences, Ulster University, C-TRIC, Altnagelvin Hospital Campus, Glenshane Road, Derry/Londonderry BT47 6SB, UK.

出版信息

Int J Mol Sci. 2021 Sep 21;22(18):10163. doi: 10.3390/ijms221810163.

Abstract

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.

摘要

儿科急性髓系白血病(AML)是一种异质性疾病,其特征是髓样前体细胞恶性转化,分化受损。四十多年来,儿科 AML 的标准治疗方法基本保持不变,再加上对儿科 AML 生物学的认识不足,限制了针对这一人群的靶向治疗的进展。近年来,随着探索这种疾病的突变和转录景观的先进基因组技术的发展,寻找儿科 AML 治疗新靶点的研究也在加速。利用现有药物的大量组合空间,为寻找儿科 AML 潜在的联合治疗方法提供了未开发的资源。我们之前设计了一种称为 AML 中相互作用化合物的多重筛选策略(Multiplex Screening for Interacting Compounds in AML,MuSICAL);使用内部设计的算法,我们通过将药物每孔 10 种药物混合的方式,在不到 4000 个孔中对 384 种 FDA 批准的化合物进行了所有两两组合的筛选。这种方法最大限度地提高了识别具有治疗潜力的新化合物组合的概率,同时最小化了成本、复制和冗余。这种筛选策略确定了磺酰脲类药物格列美脲、神经肌肉阻滞剂潘库溴铵二溴化物和长春新碱硫酸盐的三联组合,可能成为儿科 AML 的一种潜在治疗方法。我们设想这种方法可以用于各种与疾病相关的筛选,从而有效地重新利用可以迅速推向临床的药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7c1/8468645/2efc5ce3816c/ijms-22-10163-g001.jpg

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