Lizhnyak Pavel N, Ottens Andrew K
Department of Anatomy and Neurobiology, Virginia Commonwealth University School of Medicine, Richmond, VA 23298, USA.
Expert Rev Proteomics. 2015 Feb;12(1):75-82. doi: 10.1586/14789450.2015.1000869.
Effective traumatic brain injury (TBI) therapeutics remains stubbornly elusive. Efforts in the field have been challenged by the heterogeneity of clinical TBI, with greater complexity among underlying molecular phenotypes than initially conceived. Future research must confront the multitude of factors comprising this heterogeneity, representing a big data challenge befitting the coming informatics age. Proteomics is poised to serve a central role in prescriptive therapeutic development because it offers an efficient endpoint within which to assess post-TBI biochemistry. We examine rationale for multifactor TBI proteomic studies and the particular importance of temporal profiling in defining biochemical sequences and guiding therapeutic development. Finally, we offer perspective on repurposing biofluid proteomics to develop theragnostic assays with which to prescribe, monitor and assess pharmaceutics for improved translation and outcome for patients with TBI.
有效的创伤性脑损伤(TBI)治疗方法仍然难以捉摸。该领域的努力受到临床TBI异质性的挑战,其潜在分子表型的复杂性比最初设想的要大。未来的研究必须应对构成这种异质性的众多因素,这是一个适合即将到来的信息时代的大数据挑战。蛋白质组学有望在个性化治疗开发中发挥核心作用,因为它提供了一个有效的终点,可在其中评估TBI后的生物化学变化。我们研究了多因素TBI蛋白质组学研究的基本原理,以及时间分析在定义生化序列和指导治疗开发中的特殊重要性。最后,我们对重新利用生物流体蛋白质组学以开发诊断治疗分析方法提出了看法,通过这些方法可以为TBI患者开处方、监测和评估药物,以改善转化和治疗效果。