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Pharmacological targeting of endoplasmic reticulum stress in disease
Author(s) -
Stefan J. Marciniak,
Joseph E. Chambers,
David Ron
Publication year - 2021
Publication title -
nature reviews drug discovery
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.921
H-Index - 328
eISSN - 1474-1784
pISSN - 1474-1776
DOI - 10.1038/s41573-021-00320-3
Subject(s) - endoplasmic reticulum , unfolded protein response , drug discovery , drug development , homeostasis , protein folding , microbiology and biotechnology , drug , drug target , medicine , bioinformatics , neuroscience , biology , pharmacology
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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