Yin Jiayi, Li Xiaoxu, Li Fengcheng, Lu Yinjing, Zeng Su, Zhu Feng
College of Pharmaceutical Sciences, Zhejiang University, Hangzhou 310058, China.
Innovation Institute for Artificial Intelligence in Medicine of Zhejiang University, Hangzhou 310018, China.
Comput Struct Biotechnol J. 2021 Apr 21;19:2318-2328. doi: 10.1016/j.csbj.2021.04.035. eCollection 2021.
An appropriate therapeutic index is crucial for drug discovery and development since narrow therapeutic index (NTI) drugs with slight dosage variation may induce severe adverse drug reactions or potential treatment failure. To date, the shared characteristics underlying the targets of NTI drugs have been explored by several studies, which have been applied to identify potential drug targets. However, the association between the drug therapeutic index and the related disease has not been dissected, which is important for revealing the NTI drug mechanism and optimizing drug design. Therefore, in this study, two classes of disease (cancers and cardiovascular disorders) with the largest number of NTI drugs were selected, and the target property of the corresponding NTI drugs was analyzed. By calculating the biological system profiles and human protein-protein interaction (PPI) network properties of drug targets and adopting an AI-based algorithm, differentiated features between two diseases were discovered to reveal the distinct underlying mechanisms of NTI drugs in different diseases. Consequently, ten shared features and four unique features were identified for both diseases to distinguish NTI from NNTI drug targets. These computational discoveries, as well as the newly found features, suggest that in the clinical study of avoiding narrow therapeutic index in those diseases, the ability of target to be a hub and the efficiency of target signaling in the human PPI network should be considered, and it could thus provide novel guidance in the drug discovery and clinical research process and help to estimate the drug safety of cancer and cardiovascular disease.
合适的治疗指数对于药物研发至关重要,因为治疗指数窄(NTI)的药物剂量稍有变化就可能引发严重的药物不良反应或导致潜在的治疗失败。迄今为止,已有多项研究探索了NTI药物靶点的共同特征,并将其应用于识别潜在的药物靶点。然而,药物治疗指数与相关疾病之间的关联尚未得到剖析,而这对于揭示NTI药物机制和优化药物设计至关重要。因此,在本研究中,我们选择了NTI药物数量最多的两类疾病(癌症和心血管疾病),并分析了相应NTI药物的靶点特性。通过计算药物靶点的生物系统概况和人类蛋白质-蛋白质相互作用(PPI)网络特性,并采用基于人工智能的算法,发现了两种疾病之间的差异特征,以揭示NTI药物在不同疾病中的独特潜在机制。因此,确定了两种疾病共有的十个特征和四个独特特征,以区分NTI和非NTI药物靶点。这些计算发现以及新发现的特征表明,在这些疾病避免窄治疗指数的临床研究中,应考虑靶点在人类PPI网络中成为枢纽的能力和靶点信号传导效率,从而为药物研发和临床研究过程提供新的指导,并有助于评估癌症和心血管疾病药物的安全性。