个性化医疗:在患者衍生细胞培养中建立药物反应预测机器学习模型

Abbi Abdel-Rehim, Oghenejokpeme Orhobor, Gareth Griffiths, Larisa Soldatova, Ross D. King
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引用次数: 0

摘要

癌症治疗中的个性化药物概念正变得越来越重要。目前已经有了专门针对出现明确突变的肿瘤患者的药物。然而,这一领域仍处于起步阶段,个性化治疗远未成为标准治疗。个性化医疗通常与组学数据的利用联系在一起。然而,由于数据信息的多样性和规模,以及细胞内发生的无数相互作用背后的复杂性,实施多组学数据已被证明是困难的。精准医疗的另一种方法是采用基于功能的细胞概况。这包括针对患者衍生细胞筛选一系列药物。在这里,我们展示了一个概念验证,即针对高度多样化的患者衍生细胞系进行一系列药物筛选,从而为 "新患者 "确定可能的治疗方案。我们的研究表明,这种方法能根据药物对靶细胞的活性对药物进行高效排序。我们认为这种方法具有巨大的潜力,因为药物活性可以从不同的药物治疗细胞系子集中有效地推算出来,而这些细胞系并不一定来自相同的组织类型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Personalised Medicine: Establishing predictive machine learning models for drug responses in patient derived cell culture
The concept of personalised medicine in cancer therapy is becoming increasingly important. There already exist drugs administered specifically for patients with tumours presenting well-defined mutations. However, the field is still in its infancy, and personalised treatments are far from being standard of care. Personalised medicine is often associated with the utilisation of omics data. Yet, implementation of multi-omics data has proven difficult, due to the variety and scale of the information within the data, as well as the complexity behind the myriad of interactions taking place within the cell. An alternative approach to precision medicine is to employ a function-based profile of the cell. This involves screening a range of drugs against patient derived cells. Here we demonstrate a proof-of-concept, where a collection of drug screens against a highly diverse set of patient-derived cell lines, are leveraged to identify putative treatment options for a 'new patient'. We show that this methodology is highly efficient in ranking the drugs according to their activity towards the target cells. We argue that this approach offers great potential, as activities can be efficiently imputed from various subsets of the drug treated cell lines that do not necessarily originate from the same tissue type.
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