内质网
未折叠蛋白反应
药物开发
细胞生物学
药物发现
平衡
蛋白质折叠
药物靶点
药品
药理学
生物信息学
神经科学
医学
生物
作者
Stefan J. Marciniak,Joseph E. Chambers,David Ron
标识
DOI:10.1038/s41573-021-00320-3
摘要
The accumulation of misfolded proteins in the endoplasmic reticulum (ER) leads to ER stress, resulting in activation of the unfolded protein response (UPR) that aims to restore protein homeostasis. However, the UPR also plays an important pathological role in many diseases, including metabolic disorders, cancer and neurological disorders. Over the last decade, significant effort has been invested in targeting signalling proteins involved in the UPR and an array of drug-like molecules is now available. However, these molecules have limitations, the understanding of which is crucial for their development into therapies. Here, we critically review the existing ER stress and UPR-directed drug-like molecules, highlighting both their value and their limitations.
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