Development of novel prediction model for drug-induced mitochondrial toxicity by using naive Bayes classifier method

被引:31
作者
Zhang, Hui [1 ,2 ,3 ]
Yu, Peng [1 ]
Ren, Ji-Xia [2 ,3 ,4 ]
Li, Xi-Bo [1 ]
Wang, He-Li [1 ]
Ding, Lan [1 ]
Kong, Wei-Bao [1 ]
机构
[1] Northwest Normal Univ, Coll Life Sci, Lanzhou 730070, Gansu, Peoples R China
[2] Sichuan Univ, West China Med Sch, West China Hosp, State Key Lab Biotherapy, Chengdu 610041, Sichuan, Peoples R China
[3] Sichuan Univ, West China Med Sch, West China Hosp, Canc Ctr, Chengdu 610041, Sichuan, Peoples R China
[4] Liaocheng Univ, Coll Life Sci, Liaocheng 252059, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
Mitochondrial toxicity; Naive Bayes classifier; Recursive partitioning classifier; Molecular descriptors; Extended connectivity fingerprints (ECFP_6); IN-SILICO PREDICTION; ADMET EVALUATION; NEURODEGENERATIVE DISEASES; DYSFUNCTION; TARGETS; MECHANISMS; ASSAY;
D O I
10.1016/j.fct.2017.10.021
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Mitochondrial dysfunction has been considered as an important contributing factor in the etiology of drug induced organ toxicity, and even plays an important role in the pathogenesis of some diseases. The objective of this investigation was to develop a novel prediction model of drug-induced mitochondrial toxicity by using a naive Bayes classifier. For comparison, the recursive partitioning classifier prediction model was also constructed. Among these methods, the prediction performance of naive Bayes classifier established here showed best, which yielded average overall prediction accuracies for the internal 5-fold cross validation of the training set and external test set were 95 +/- 0.6% and 81 +/- 1.1%, respectively. In addition, four important molecular descriptors and some representative substructures of toxicants produced by ECFP_6 fingerprints were identified. We hope the established naive Bayes prediction model can be employed for the mitochondrial toxicity assessment, and these obtained important information of mitochondrial toxicants can provide guidance for medicinal chemists working in drug discovery and lead optimization.
引用
收藏
页码:122 / 129
页数:8
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