Wei Yu-da, Li Shuang, Liu Gai-gai, Zhang Yong-xian, Ding Qiu-rong
Institute for Nutritional Sciences, Shanghai Institutes for Biological Sciences, Shanghai 200031, China.
Yi Chuan. 2015 Oct;37(10):983-91. doi: 10.16288/j.yczz.15-239.
Precision medicine emerges as a new approach that takes into account individual variability. The successful conduct of precision medicine requires the use of precise disease models. Human pluripotent stem cells (hPSCs), as well as adult stem cells, can be differentiated into a variety of human somatic cell types that can be used for research and drug screening. The development of genome editing technology over the past few years, especially the CRISPR/Cas system, has made it feasible to precisely and efficiently edit the genetic background. Therefore, disease modeling by using a combination of human stem cells and genome editing technology has offered a new platform to generate " personalized " disease models, which allow the study of the contribution of individual genetic variabilities to disease progression and the development of precise treatments. In this review, recent advances in the use of genome editing in human stem cells and the generation of stem cell models for rare diseases and cancers are discussed.
精准医学作为一种考虑个体差异的新方法应运而生。成功开展精准医学需要使用精确的疾病模型。人类多能干细胞(hPSC)以及成体干细胞可分化为多种人类体细胞类型,可用于研究和药物筛选。过去几年基因组编辑技术的发展,尤其是CRISPR/Cas系统,使得精确高效地编辑遗传背景成为可能。因此,结合人类干细胞和基因组编辑技术进行疾病建模提供了一个新平台,以生成“个性化”疾病模型,从而能够研究个体遗传变异对疾病进展的影响以及开发精准治疗方法。在本综述中,将讨论人类干细胞基因组编辑应用的最新进展以及罕见病和癌症干细胞模型的生成。