Edward Doisy Department of Biochemistry and Molecular Biology.
Departments of Internal Medicine and Pharmacology & Physiology, Saint Louis University School of Medicine, St. Louis, Missouri.
Mo Med. 2021 Jul-Aug;118(4):340-345.
Most neurodegenerative disorders afflict the ageing population and are often incurable. Therefore, therapeutic development is a major focus in biomedical research. We highlight a new class of drugs, RNA molecules, to control gene expression and decrease neurotoxicity. Their efficacy is shown in pre-clinical studies, clinical trials and in cases of approved patient treatment. As the number of RNA-based strategies increases, so does the promise of targeting more disease-associated genes through a variety of different mechanisms.
大多数神经退行性疾病都影响老年人群体,而且往往无法治愈。因此,治疗方法的开发是生物医学研究的主要重点。我们强调了一类新的药物,即 RNA 分子,它们可以控制基因表达并降低神经毒性。它们的疗效已在临床前研究、临床试验以及经批准的患者治疗案例中得到证实。随着基于 RNA 的策略数量的增加,通过各种不同的机制靶向更多与疾病相关的基因的前景也越来越大。