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H-RACS: a handy tool to rank anti-cancer synergistic drugs

机译:H-RACS:一个方便的工具用于排名抗癌协同毒品

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摘要

Though promising, identifying synergistic combinations from a large pool of candidate drugs remains challenging for cancer treatment. Due to unclear mechanism and limited confirmed cases, only a few computational algorithms are able to predict drug synergy. Yet they normally require the drug-cell treatment results as an essential input, thus exclude the possibility to pre-screen those unexplored drugs without cell treatment profiling. Based on the largest dataset of 33,574 combinational scenarios, we proposed a handy webserver, H-RACS, to overcome the above problems. Being loaded with chemical structures and target information, H-RACS can recommend potential synergistic pairs between candidate drugs on 928 cell lines of 24 prevalent cancer types. A high model performance was achieved with AUC of 0.89 on independent combinational scenarios. On the second independent validation of DREAM dataset, H-RACS obtained precision of 67% among its top 5% ranking list. When being tested on new combinations and new cell lines, H-RACS showed strong extendibility with AUC of 0.84 and 0.81 respectively. As the first online server freely accessible at http://www.badd-cao.net/h-racs, H-RACS may promote the pre-screening of synergistic combinations for new chemical drugs on unexplored cancers.
机译:虽然有前途,但识别来自一大堆候选药物的协同组合仍然挑战癌症治疗。由于机制和有限的确认情况下,只有少数计算算法能够预测药物协同作用。然而,它们通常需要药物细胞治疗结果作为必要的输入,因此排除了在没有细胞治疗分析的情况下预先筛选那些未探究药物的可能性。基于33,574个组合场景的最大数据集,我们提出了一个方便的网络服务器,H-RAC,来克服上述问题。加载化学结构和目标信息,H-Racs可以推荐候选药物之间的潜在协同对,在928种普遍癌症类型的细胞系上。在独立组合情景中为0.89的AUC实现了高模型性能。在梦想数据集的第二个独立验证中,H-RACS在其前5%排名列表中获得了67%的精度。在新组合和新的细胞系上进行测试时,H-RACS分别显示出与0.84和0.81的AUC的强大可扩展性。作为第一个在线服务器免费访问http://www.badd-cao.net/h-racs,H-Racs可能会促进在未开发的癌症上进行新化学药物的协同组合的预筛选。

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