个体化医疗中药物反应预测的矩阵补全方法

Giang T. T. Nguyen, Duc-Hau Le
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引用次数: 5

摘要

个性化医疗的一个重要目标是根据患者的分子特征为他们提供正确的治疗。几个大型项目已经启动,并产生了大量的人类细胞系组学和药物反应数据。这些项目对于在对人体进行临床试验之前在细胞系上测试药物反应非常有用。然而,一系列药物和细胞系尚未经过测试。因此,许多计算方法试图预测这样的反应,以最大限度地提高治疗效率和最小化副作用。这些方法不仅利用已知的药物-细胞系反应,而且利用药物之间和细胞系之间的相似性。然而,用于计算细胞系相似性的细胞系组学数据通常因平台而异,导致结果不一致。因此,在本研究中,我们提出了一种基于矩阵补全技术的药物反应预测方法(MCDRP),该方法仅使用已知的药物-细胞系反应信息来预测未经测试的细胞系的药物反应。该方法不仅可以同时计算一种药物的反应,还可以同时计算所有药物的反应。与其他方法相比,我们发现我们的方法获得了更好的IC50响应测量性能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A matrix completion method for drug response prediction in personalized medicine
One of the significant goals of personalized medicine is to provide the right treatment to patients based on their molecular features. Several big projects have been launched and generated a large amount of -omics and drug response data for cell lines of the human. These projects are very useful for testing of drug responses on cell lines before employing clinical trials on humans. However, a range of drugs and cell lines have not been tested yet. Thus, many computational methods attempt to predict such the responses to maximize the treatment efficiency and to minimize side-effects. These methods use not only known drug -- cell lines responses but also the similarity between drugs and between cell lines. Nevertheless, -omics data for cell lines which is used to calculate the cell-line similarities usually varies among platforms leading to heterogeneous results. Therefore, in this study, we propose a drug response prediction method (MCDRP) based on a matrix completion technique using only known drug -- cell lines response information to predict drug responses for untested cell lines. The method can impute responses for not only one at time but also all drugs simultaneously. In comparison with other methods, we found that our method achieved better performance for IC50 response measurement.
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