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诱导多能干细胞:神经疾病的临床前药物研究工具。

iPSCs: A Preclinical Drug Research Tool for Neurological Disorders.

机构信息

Institute for Biomedical Research and Innovation (IRIB), Italian National Research Council, 95126 Catania, Italy.

Department of Biomedical and Biotechnological Sciences (BIOMETEC), Section of Pharmacology, University of Catania, 95123 Catania, Italy.

出版信息

Int J Mol Sci. 2021 Apr 27;22(9):4596. doi: 10.3390/ijms22094596.

Abstract

The development and commercialization of new drugs is an articulated, lengthy, and very expensive process that proceeds through several steps, starting from target identification, screening new leading compounds for testing in preclinical studies, and subsequently in clinical trials to reach the final approval for therapeutic use. Preclinical studies are usually performed using both cell cultures and animal models, although they do not completely resume the complexity of human diseases, in particular neurodegenerative conditions. To this regard, stem cells represent a powerful tool in all steps of drug discovery. The recent advancement in induced Pluripotent Stem Cells (iPSCs) technology has opened the possibility to obtain patient-specific disease models for drug screening and development. Here, we report the use of iPSCs as a disease model for drug development in the contest of neurological disorders, including Alzheimer's (AD) and Parkinson's disease (PD), Amyotrophic lateral Sclerosis (ALS), and Fragile X syndrome (FRAX).

摘要

新药的开发和商业化是一个复杂、漫长且非常昂贵的过程,它要经过多个步骤,从目标确定开始,筛选新的先导化合物进行临床前研究,并随后进行临床试验,最终获得治疗用途的批准。临床前研究通常使用细胞培养和动物模型进行,但它们并不能完全重现人类疾病的复杂性,特别是神经退行性疾病。在这方面,干细胞在药物发现的所有步骤中都是一种强大的工具。诱导多能干细胞 (iPSC) 技术的最新进展为药物筛选和开发提供了获得患者特异性疾病模型的可能性。在这里,我们报告了使用 iPSC 作为神经紊乱疾病(包括阿尔茨海默病 (AD) 和帕金森病 (PD)、肌萎缩性侧索硬化症 (ALS) 和脆性 X 综合征 (FRAX))药物开发的疾病模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7c2/8123805/07f8f0dbcb0b/ijms-22-04596-g001.jpg

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