Department of Electrical and Computer Engineering, University of Connecticut, 371 Fairfield Way, Storrs, CT, 06269, USA.
NPJ Syst Biol Appl. 2022 Oct 3;8(1):37. doi: 10.1038/s41540-022-00247-4.
Omics-based approaches have become increasingly influential in identifying disease mechanisms and drug responses. Considering that diseases and drug responses are co-expressed and regulated in the relevant omics data interactions, the traditional way of grabbing omics data from single isolated layers cannot always obtain valuable inference. Also, drugs have adverse effects that may impair patients, and launching new medicines for diseases is costly. To resolve the above difficulties, systems biology is applied to predict potential molecular interactions by integrating omics data from genomic, proteomic, transcriptional, and metabolic layers. Combined with known drug reactions, the resulting models improve medicines' therapeutical performance by re-purposing the existing drugs and combining drug molecules without off-target effects. Based on the identified computational models, drug administration control laws are designed to balance toxicity and efficacy. This review introduces biomedical applications and analyses of interactions among gene, protein and drug molecules for modeling disease mechanisms and drug responses. The therapeutical performance can be improved by combining the predictive and computational models with drug administration designed by control laws. The challenges are also discussed for its clinical uses in this work.
基于组学的方法在识别疾病机制和药物反应方面变得越来越有影响力。考虑到疾病和药物反应在相关组学数据相互作用中共同表达和调节,从单个孤立层抓取组学数据的传统方法并不总是能获得有价值的推断。此外,药物有不良反应,可能会损害患者,而且开发针对疾病的新药成本很高。为了解决上述困难,系统生物学被应用于通过整合基因组、蛋白质组、转录组和代谢组学等层面的组学数据来预测潜在的分子相互作用。结合已知的药物反应,所得到的模型通过重新利用现有药物和结合没有脱靶效应的药物分子来提高药物的治疗性能。基于所确定的计算模型,设计药物管理控制律来平衡毒性和疗效。本综述介绍了用于建模疾病机制和药物反应的基因、蛋白质和药物分子相互作用的生物医学应用和分析。通过将预测和计算模型与控制律设计的药物管理相结合,可以提高治疗效果。本工作还讨论了其在临床应用中的挑战。