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利用诱导多能干细胞进行疾病建模和药物发现的新时代。

A new era of disease modeling and drug discovery using induced pluripotent stem cells.

机构信息

College of Pharmacy, Chung-Ang University, Seoul, 06974, Korea.

出版信息

Arch Pharm Res. 2017 Jan;40(1):1-12. doi: 10.1007/s12272-016-0871-0. Epub 2016 Dec 5.

Abstract

In 2006, Shinya Yamanaka first reported that in vitro reprogramming of somatic cells toward pluripotency was achieved by simple induction of specific transcription factors. Induced pluripotent stem cell (iPSC) technology has since revolutionized the ways in which we explore the mechanisms of human diseases and develop therapeutics. Here, I describe the recent advances in human iPSC-based disease modeling and drug discovery and discuss the current challenges. Additionally, I outline potential future applications of human iPSCs in classifying patients based on their response to drugs in clinical trials and elucidating optimal patient-specific therapeutic strategies, which will contribute to reduced attrition rates and the development of precision medicine.

摘要

2006 年,Shinya Yamanaka 首次报道,通过简单诱导特定转录因子,可将体细胞在体外重编程为多能性细胞。诱导多能干细胞(iPSC)技术彻底改变了我们探索人类疾病机制和开发治疗方法的方式。在这里,我描述了基于人类 iPSC 的疾病建模和药物发现的最新进展,并讨论了当前的挑战。此外,我概述了人类 iPSC 在临床试验中根据患者对药物的反应对患者进行分类和阐明最佳患者特异性治疗策略的潜在未来应用,这将有助于降低淘汰率和开发精准医学。

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