Lin Fan, Li Zilin, Hua Yunfen, Lim Yoon Pin
a Department of Cell Biology , Nanjing Medical University , Nanjing , China.
b Department of Biochemistry , Yong Loo Lin School of Medicine, National University of Singapore , Singapore.
Expert Rev Proteomics. 2016;13(4):411-20. doi: 10.1586/14789450.2016.1164043.
Most recently approved anti-cancer drugs by the US FDA are targeted therapeutic agents and this represents an important trend for future anticancer therapy. Unlike conventional chemotherapy that rarely considers individual differences, it is crucial for targeted therapies to identify the beneficial subgroup of patients for the treatment. Currently, genomics and transcriptomics are the major 'omic' analytics used in studies of drug response prediction. However, proteomic profiling excels both in its advantages of directly detecting an instantaneous dynamic of the whole proteome, which contains most current diagnostic markers and therapeutic targets. Moreover, proteomic profiling improves understanding of the mechanism for drug resistance and helps finding optimal combination therapy. This article reviews the recent success of applications of proteomic analytics in predicting the response to targeted anticancer therapeutics, and discusses the potential avenues and pitfalls of proteomic platforms and techniques used most in the field.
美国食品药品监督管理局(FDA)最近批准的抗癌药物大多是靶向治疗药物,这代表了未来抗癌治疗的一个重要趋势。与很少考虑个体差异的传统化疗不同,靶向治疗确定受益患者亚组进行治疗至关重要。目前,基因组学和转录组学是药物反应预测研究中主要使用的“组学”分析方法。然而,蛋白质组分析在直接检测整个蛋白质组的瞬时动态方面具有优势,而整个蛋白质组包含了大多数当前的诊断标志物和治疗靶点。此外,蛋白质组分析有助于深入了解耐药机制,并有助于找到最佳联合治疗方案。本文综述了蛋白质组分析在预测靶向抗癌治疗反应方面的近期应用成果,并讨论了该领域最常用的蛋白质组平台和技术的潜在途径及陷阱。