Zhang Hui, Ren Ji-Xia, Kang Yan-Li, Bo Peng, Liang Jun-Yu, Ding Lan, Kong Wei-Bao, Zhang Ji
College of Life Science, Northwest Normal University, Lanzhou, Gansu, 730070, PR China; State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, West China Medical School, Sichuan University, Chengdu, Sichuan, 610041, PR China.
State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, West China Medical School, Sichuan University, Chengdu, Sichuan, 610041, PR China; College of Life Science, Liaocheng University, Liaocheng, Shandong, 252059, PR China.
Reprod Toxicol. 2017 Aug;71:8-15. doi: 10.1016/j.reprotox.2017.04.005. Epub 2017 Apr 18.
Toxicological testing associated with developmental toxicity endpoints are very expensive, time consuming and labor intensive. Thus, developing alternative approaches for developmental toxicity testing is an important and urgent task in the drug development filed. In this investigation, the naïve Bayes classifier was applied to develop a novel prediction model for developmental toxicity. The established prediction model was evaluated by the internal 5-fold cross validation and external test set. The overall prediction results for the internal 5-fold cross validation of the training set and external test set were 96.6% and 82.8%, respectively. In addition, four simple descriptors and some representative substructures of developmental toxicants were identified. Thus, we hope the established in silico prediction model could be used as alternative method for toxicological assessment. And these obtained molecular information could afford a deeper understanding on the developmental toxicants, and provide guidance for medicinal chemists working in drug discovery and lead optimization.
与发育毒性终点相关的毒理学测试成本高昂、耗时且劳动强度大。因此,开发发育毒性测试的替代方法是药物开发领域一项重要且紧迫的任务。在本研究中,应用朴素贝叶斯分类器开发了一种新型发育毒性预测模型。通过内部5折交叉验证和外部测试集对所建立的预测模型进行评估。训练集内部5折交叉验证和外部测试集的总体预测结果分别为96.6%和82.8%。此外,还确定了四种简单描述符和一些发育毒物的代表性子结构。因此,我们希望所建立的计算机预测模型可作为毒理学评估的替代方法。并且这些获得的分子信息能够加深对发育毒物的理解,并为从事药物发现和先导优化的药物化学家提供指导。