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Predicting Combinative Drug Pairs via Integrating Heterogeneous Features for Both Known and New Drugs

机译:通过对已知和新药的整合异质特征来预测组合药物对

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An ordinary disease caused by the anomaly of expression level of an individual gene, can be treated by a specific drug, which regulates the gene's expression. However, this single-drug treatment has very low effectiveness on complex diseases [1], which usually involve multiple genes and pathways of the metabolic network. Drug combination, as one of multiple-target treatments, has demonstrated its effectiveness in treating complex diseases, such as HIV/AIDS [2] and colorectal cancer [3]. However, it is still costly and time-consuming in clinical trials to find an effective combination of individual drugs. Fortunately, both the number of approved drug combinations [4] and the amount of available heterogeneous information about drugs are increasing. It became feasible to develop computational approaches to predict potential candidates of drug pairs for the treatments of complex diseases [5, 6].
机译:由个体基因的表达水平的异常引起的普通疾病可以通过特定药物治疗,该药物调节基因的表达。然而,这种单药治疗对复杂疾病的有效性非常低,这通常涉及代谢网络的多种基因和途径。药物组合作为多目标治疗之一,已经证明其在治疗复杂疾病的有效性,例如艾滋病毒/艾滋病[2]和结肠直肠癌[3]。然而,在临床试验中仍然昂贵且耗时,以找到个体药物的有效组合。幸运的是,经批准的药物组合的数量[4]和有关药物的可用异质信息的数量正在增加。开发计算方法是可行的,以预测复杂疾病治疗的药物对的潜在候选者[5,6]。

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