Bongarzone Salvatore, Staderini Matteo, Bolognesi Maria Laura
Institute for Research in Biomedicine, Barcelona Science Park, Baldiri Reixac 10, 08028 Barcelona, Spain.
Future Med Chem. 2014 Jun;6(9):1017-29. doi: 10.4155/fmc.14.56.
Prion diseases (PrDs) are fatal neurodegenerative disorders, for which no effective therapeutic and diagnostic tools exist. The main pathogenic event has been identified as the misfolding of a disease-associated prion protein. Nevertheless, pathogenesis seems to involve an intricate array of concomitant processes. Thus, it may be unlikely that drugs acting on single targets can effectively control PrDs. In addition, diagnosis occurs late in the disease process, by which point it is difficult to determine a successful therapeutic intervention. In this context, multitarget ligands (MTLs) and theranostic ligands (TLs) emerge for their potential to effectively cure and diagnose PrDs. In this review, we discuss the medicinal chemistry challenges of identifying novel MTLs and TLs against PrDs, and envision their impact on prion drug discovery.
朊病毒病(PrDs)是致命的神经退行性疾病,目前尚无有效的治疗和诊断工具。主要致病事件已被确定为与疾病相关的朊病毒蛋白的错误折叠。然而,发病机制似乎涉及一系列复杂的伴随过程。因此,作用于单一靶点的药物不太可能有效控制朊病毒病。此外,诊断在疾病过程后期进行,此时很难确定成功的治疗干预措施。在此背景下,多靶点配体(MTLs)和诊疗配体(TLs)因其有效治愈和诊断朊病毒病的潜力而出现。在本综述中,我们讨论了识别针对朊病毒病的新型MTLs和TLs所面临的药物化学挑战,并展望了它们对朊病毒药物发现的影响。