Functional Genomics Center, Institute of Neurological Sciences, Italian National Research Council, Catania, Italy.
Curr Pharm Des. 2011;17(3):190-203. doi: 10.2174/138161211795049688.
The advent of "systems biology" has highlighted that any function of a biological system is rarely attributable to a single molecule or a single process. Hence, complex processes, such as apoptosis and survival, depend on the activity of an integrated network of genes and their encoded proteins, which almost never work alone but interact with each other in highly structured and incredibly complex ways. With the completion of genome sequencing in humans and model organisms, and the advent of DNA microarray technology, the transcriptional cascades and gene networks regulating neuronal apoptosis and survival are being elucidated providing new potential pharmacological targets. The emerging challenge is the effective selection of the myriad of targets to identify those with the most therapeutic utility. The present review will illustrate how the identification, prioritization and validation of preclinical therapeutics can be achieved through genomic analysis of critical pathways and networks in neuronal apoptosis and survival.
“系统生物学”的出现强调了生物系统的任何功能都很少归因于单个分子或单个过程。因此,复杂的过程,如细胞凋亡和存活,取决于基因及其编码蛋白的整合网络的活性,这些基因及其编码蛋白几乎从不单独工作,而是以高度结构化和极其复杂的方式相互作用。随着人类和模式生物基因组测序的完成,以及 DNA 微阵列技术的出现,调控神经元凋亡和存活的转录级联和基因网络正在被阐明,为新的潜在药物靶点提供了依据。当前的挑战是有效地选择无数的靶点,以确定那些具有最大治疗效用的靶点。本综述将说明如何通过对神经元凋亡和存活的关键途径和网络进行基因组分析来鉴定、优先考虑和验证临床前治疗药物。