Harnessing human genetics and stem cells for precision cardiovascular medicine

被引:4
|
作者
Caudal, Arianne [1 ,2 ]
Snyder, Michael P. [3 ]
Wu, Joseph C. [1 ,2 ,4 ]
机构
[1] Stanford Univ, Stanford Cardiovasc Inst, Sch Med, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Med, Div Cardiovasc Med, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Dept Genet, Stanford, CA 94305 USA
[4] Greenstone Biosci, Palo Alto, CA 94304 USA
来源
CELL GENOMICS | 2024年 / 4卷 / 02期
基金
美国国家卫生研究院;
关键词
HUMAN CARDIAC ORGANOIDS; HYPERTROPHIC CARDIOMYOPATHY; ENDOTHELIAL DYSFUNCTION; DILATED CARDIOMYOPATHY; INDUCED CARDIOTOXICITY; CARDIOMYOCYTES; MATURATION; DISEASE; MUTATIONS; VARIANT;
D O I
10.1016/j.xgen.2023.100445
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Human induced pluripotent stem cell (iPSC) platforms are valuable for biomedical and pharmaceutical research by providing tissue-specific human cells that retain patients' genetic integrity and display disease phenotypes in a dish. Looking forward, combining iPSC phenotyping platforms with genomic and screening technologies will continue to pave new directions for precision medicine, including genetic prediction, visualization, and treatment of heart disease. This review summarizes the recent use of iPSC technology to unpack the influence of genetic variants in cardiovascular pathology. We focus on various state -of -the -art genomic tools for cardiovascular therapies-including the expansion of genetic toolkits for molecular interrogation, in vitro population studies, and function-based drug screening-and their current applications in patient- and genome-edited iPSC platforms that are heralding new avenues for cardiovascular research.
引用
收藏
页数:12
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