诱导多能干细胞
基因组编辑
基因组
精密医学
计算生物学
生物
人类基因组
疾病
人类疾病
基因
遗传学
胚胎干细胞
医学
病理
作者
Benjamin Steyer,Evan Cory,Krishanu Saha
标识
DOI:10.1016/j.ddtec.2018.02.001
摘要
Many avenues exist for human pluripotent stem cells (hPSCs) to impact medical care, but they may have their greatest impact on the development of precision medicine. Recent advances in genome editing and stem cell technology have enabled construction of clinically-relevant, genotype-specific "disease-in-a-dish" models. In this review, we outline the use of genome-edited hPSCs in precision disease modeling and drug screening as well as describe methodological advances in scarless genome editing. Scarless genome-editing approaches are attractive for genotype-specific disease modeling as only the intended DNA base-pair edits are incorporated without additional genomic modification. Emerging evidentiary standards for development and approval of precision therapies are likely to increase application of disease models derived from genome-edited hPSCs.
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