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A Review of Human Pluripotent Stem Cell-Derived Cardiomyocytes for High-Throughput Drug Discovery Cardiotoxicity Screening and Publication Standards

机译:用于高通量药物发现心脏毒性筛查和出版标准的人多能干细胞衍生心肌细胞的综述

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摘要

Drug attrition rates have increased in past years, resulting in growing costs for the pharmaceutical industry and consumers. The reasons for this include the lack of in vitro models that correlate with clinical results, and poor preclinical toxicity screening assays. The in vitro production of human cardiac progenitor cells and cardiomyocytes from human pluripotent stem cells provides an amenable source of cells for applications in drug discovery, disease modeling, regenerative medicine, and cardiotoxicity screening. In addition, the ability to derive human induced pluripotent stem cells from somatic tissues, combined with current high-throughput screening and pharmacogenomics, may help realize the use of these cells to fulfill the potential of personalized medicine. In this review, we discuss the use of pluripotent stem cell-derived cardiomyocytes for drug discovery and cardiotoxicity screening, as well as current hurdles that must be overcome for wider clinical applications of this promising approach.
机译:过去几年中,药物消耗率有所增加,导致制药业和消费者的成本不断增加。其原因包括缺乏与临床结果相关的体外模型,以及不良的临床前毒性筛选分析。由人多能干细胞体外产生人心脏祖细胞和心肌细胞提供了可用于药物发现,疾病建模,再生医学和心脏毒性筛查的细胞来源。另外,从体细胞组织中提取人诱导的多能干细胞的能力,与当前的高通量筛选和药物基因组学相结合,可能有助于实现这些细胞的用途,以实现个性化医学的潜力。在这篇综述中,我们讨论了将多能干细胞衍生的心肌细胞用于药物发现和心脏毒性筛查,以及目前对于该有希望的方法的更广泛临床应用必须克服的障碍。

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