Kabir Md Humayun, O'Connor Michael D
School of Medicine, Western Sydney University, Campbelltown, NSW, Australia.
Department of Computer Science and Engineering, University of Rajshahi, Rajshahi, Bangladesh.
Biophys Rev. 2019 Feb;11(1):41-50. doi: 10.1007/s12551-018-0486-4. Epub 2019 Jan 25.
Identification of new drug and cell therapy targets for disease treatment will be facilitated by a detailed molecular understanding of normal and disease development. Human pluripotent stem cells can provide a large in vitro source of human cell types and, in a growing number of instances, also three-dimensional multicellular tissues called organoids. The application of stem cell technology to discovery and development of new therapies will be aided by detailed molecular characterisation of cell identity, cell signalling pathways and target gene networks. Big data or 'omics' techniques-particularly transcriptomics and proteomics-facilitate cell and tissue characterisation using thousands to tens-of-thousands of genes or proteins. These gene and protein profiles are analysed using existing and/or emergent bioinformatics methods, including a growing number of methods that compare sample profiles against compendia of reference samples. This review assesses how compendium-based analyses can aid the application of stem cell technology for new therapy development. This includes via robust definition of differentiated stem cell identity, as well as elucidation of complex signalling pathways and target gene networks involved in normal and diseased states.
对正常和疾病发展的详细分子理解将有助于识别用于疾病治疗的新药物和细胞治疗靶点。人类多能干细胞可以提供大量体外来源的人类细胞类型,并且在越来越多的情况下,还能提供称为类器官的三维多细胞组织。对细胞身份、细胞信号通路和靶基因网络进行详细的分子表征,将有助于干细胞技术在新疗法发现和开发中的应用。大数据或“组学”技术——特别是转录组学和蛋白质组学——有助于利用数千到数万个基因或蛋白质对细胞和组织进行表征。使用现有的和/或新兴的生物信息学方法对这些基因和蛋白质谱进行分析,包括越来越多的将样本谱与参考样本集进行比较的方法。本综述评估了基于样本集的分析如何有助于干细胞技术在新疗法开发中的应用。这包括通过对分化干细胞身份的可靠定义,以及阐明正常和疾病状态下涉及的复杂信号通路和靶基因网络。