Wu Qihui, Su Shijie, Cai Chuipu, Xu Lina, Fan Xiude, Ke Hanzhong, Dai Zhao, Fang Shuhuan, Zhuo Yue, Wang Qi, Pan Huafeng, Gu Yong, Fang Jiansong
Clinical Research Center, Hainan Provincial Hospital of Traditional Chinese Medicine, Guangzhou University of Chinese Medicine, Haikou, China.
Science and Technology Innovation Center, Guangzhou University of Chinese Medicine, Guangzhou, China.
Comput Struct Biotechnol J. 2023 Feb 24;21:1907-1920. doi: 10.1016/j.csbj.2023.02.041. eCollection 2023.
Despite the massive investment in Alzheimer's disease (AD), there are still no disease-modifying treatments (DMTs) for AD. One major reason is attributed to the limitation of clinical "one-size-fits-all" approach, since the same AD treatment solely based on clinical diagnosis was unlikely to achieve good clinical efficacy. In recent years, computational approaches based on multiomics data have provided an unprecedented opportunity for drug discovery since they can substantially lower the costs and boost the efficiency. In this study, we intended to identify potential drug candidates for different pathological stages of AD by computationally repurposing Food and Drug Administration (FDA) approved drugs. First, we assembled gene expression data from three different AD pathological stages, which include mild cognitive impairment (MCI) and early and late stages of AD (EAD, LAD). We next quantified the network distances between drug target networks and AD modules by utilizing a network proximity approach, and identified 193 candidates that possessed significant associations with AD. After searching for previous literature evidence, 63 out of 193 (32.6%) predicted drugs were demonstrated to exert therapeutic effects on AD. We further explored the novel mechanism of action (MOA) for these drug candidates by determining the specific brain cells they might function on based on AD patient single cell transcriptomic data. Additionally, we selected several promising candidates that could cross the blood brain barrier together with confirmed neuroprotective effects, and subsequently determined the antioxidative activity of these compounds. Experimental results showed that azathioprine decreased the reactive oxygen species (ROS) and malondialdehyde (MDA) levels and improved the superoxide dismutase (SOD) activity in APP-SH-SY5Y cells. Finally, we deciphered the potential MOA of azathioprine against AD via network analysis and validated several apoptosis-related proteins (Caspase 3, Cleaved Caspase 3, Bax, Bcl2) through western blotting. In summary, this study presented an effective computational strategy utilizing omics data for AD drug repurposing, which provides a new perspective for drug discovery and development.
尽管在阿尔茨海默病(AD)研究上投入巨大,但目前仍没有针对AD的疾病修饰疗法(DMTs)。一个主要原因是临床“一刀切”方法存在局限性,因为仅基于临床诊断的相同AD治疗不太可能取得良好的临床疗效。近年来,基于多组学数据的计算方法为药物发现提供了前所未有的机会,因为它们可以大幅降低成本并提高效率。在本研究中,我们旨在通过对美国食品药品监督管理局(FDA)批准的药物进行计算性重新利用,来识别AD不同病理阶段的潜在候选药物。首先,我们收集了来自三个不同AD病理阶段的基因表达数据,包括轻度认知障碍(MCI)以及AD的早期和晚期(EAD、LAD)。接下来,我们利用网络接近度方法量化了药物靶标网络与AD模块之间的网络距离,并确定了193个与AD有显著关联的候选药物。在检索先前的文献证据后,193个预测药物中有63个(32.6%)被证明对AD有治疗作用。我们通过基于AD患者单细胞转录组数据确定这些候选药物可能作用的特定脑细胞,进一步探索了它们的新作用机制(MOA)。此外,我们选择了几种有前景的能够穿过血脑屏障并具有已证实的神经保护作用的候选药物,随后测定了这些化合物的抗氧化活性。实验结果表明,硫唑嘌呤降低了APP-SH-SY5Y细胞中的活性氧(ROS)和丙二醛(MDA)水平,并提高了超氧化物歧化酶(SOD)活性。最后,我们通过网络分析解读了硫唑嘌呤针对AD的潜在作用机制,并通过蛋白质印迹法验证了几种凋亡相关蛋白(Caspase 3、裂解的Caspase 3、Bax、Bcl2)。总之,本研究提出了一种利用组学数据进行AD药物重新利用的有效计算策略,为药物发现和开发提供了新的视角。