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处于神经元凋亡与存活交叉点的药物靶点识别

Drug target identification at the crossroad of neuronal apoptosis and survival.

作者信息

Maino Barbara, Paparone Simona, Severini Cinzia, Ciotti Maria Teresa, D'agata Velia, Calissano Pietro, Cavallaro Sebastiano

机构信息

a Institute of Neurological Sciences , Italian National Research Council , Catania , Italy.

b Institute of Cell Biology and Neurobiology , Italian National Research Council , Roma , Italy.

出版信息

Expert Opin Drug Discov. 2017 Mar;12(3):249-259. doi: 10.1080/17460441.2017.1280023. Epub 2017 Jan 23.

DOI:10.1080/17460441.2017.1280023
PMID:28067072
Abstract

Inappropriate activation of apoptosis may contribute to neurodegeneration, a multifaceted process that results in various chronic disorders, including Alzheimer's and Parkinson's diseases. Several in vitro and in vivo studies demonstrated that neuronal apoptosis is a multi-pathway cell-death program that requires RNA synthesis. Thus, transcriptionally activated genes whose products induce cell death can be triggered by different stimuli and antagonized by neurotrophic factors. Systems biology is now unveiling the series of intracellular signaling pathways and key drug targets at the intersection of neuronal apoptosis and survival. Areas covered: This review introduces a genomic approach that can be used to elucidate the systems biology of neuronal apoptosis and survival, and to rationally select drug targets, no longer oriented to emulate the action of growth factors at the membrane receptor level, but rather to modulate their downstream signals. Expert opinion: The advent of genomics is offering an unprecedented opportunity to explore how the delicate balance between apoptosis and survival-inducing signals triggers a transcriptional program. Characterization of this program can be useful to identify potential pharmacological targets for existing drugs. Such knowledge might pave the way towards an innovative pharmacology.

摘要

细胞凋亡的不适当激活可能导致神经退行性变,这是一个多方面的过程,会引发各种慢性疾病,包括阿尔茨海默病和帕金森病。多项体外和体内研究表明,神经元凋亡是一个需要RNA合成的多途径细胞死亡程序。因此,其产物诱导细胞死亡的转录激活基因可由不同刺激触发,并受到神经营养因子的拮抗作用。系统生物学目前正在揭示神经元凋亡与存活交叉点处的一系列细胞内信号通路和关键药物靶点。涵盖领域:本综述介绍了一种基因组学方法,该方法可用于阐明神经元凋亡与存活的系统生物学,并合理选择药物靶点,不再旨在模拟生长因子在膜受体水平的作用,而是调节其下游信号。专家观点:基因组学的出现为探索凋亡与存活诱导信号之间的微妙平衡如何触发转录程序提供了前所未有的机会。对该程序的表征有助于识别现有药物的潜在药理学靶点。此类知识可能为创新药理学铺平道路。

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