TY - JOUR
T1 - Targeting Necrosis
T2 - Elastase-like Protease Inhibitors Curtail Necrotic Cell Death Both in Vitro and in Three in Vivo Disease Models
AU - Khalfin, Boris
AU - Lichtenstein, Alexandra
AU - Albeck, Amnon
AU - Nathan, Ilana
N1 - Publisher Copyright:
© 2021 American Chemical Society. All rights reserved.
PY - 2021/2/11
Y1 - 2021/2/11
N2 - Necrosis is the main mode of cell death, which leads to multiple clinical conditions affecting hundreds of millions of people worldwide. Its molecular mechanisms are poorly understood, hampering therapeutics development. Here, we identify key proteolytic activities essential for necrosis using various biochemical approaches, enzymatic assays, medicinal chemistry, and siRNA library screening. These findings provide strategies to treat and prevent necrosis, including known medicines used for other indications, siRNAs, and establish a platform for the design of new inhibitory molecules. Indeed, inhibitors of these pathways demonstrated protective activity in vitro and in vivo in animal models of traumatic brain injury, acute myocardial infarction, and drug-induced liver toxicity. Consequently, this study may pave the way for the development of novel therapies for the treatment, inhibition, or prevention of a large number of hitherto untreatable diseases.
AB - Necrosis is the main mode of cell death, which leads to multiple clinical conditions affecting hundreds of millions of people worldwide. Its molecular mechanisms are poorly understood, hampering therapeutics development. Here, we identify key proteolytic activities essential for necrosis using various biochemical approaches, enzymatic assays, medicinal chemistry, and siRNA library screening. These findings provide strategies to treat and prevent necrosis, including known medicines used for other indications, siRNAs, and establish a platform for the design of new inhibitory molecules. Indeed, inhibitors of these pathways demonstrated protective activity in vitro and in vivo in animal models of traumatic brain injury, acute myocardial infarction, and drug-induced liver toxicity. Consequently, this study may pave the way for the development of novel therapies for the treatment, inhibition, or prevention of a large number of hitherto untreatable diseases.
UR - http://www.scopus.com/inward/record.url?scp=85101433123&partnerID=8YFLogxK
U2 - 10.1021/acs.jmedchem.0c01683
DO - 10.1021/acs.jmedchem.0c01683
M3 - Article
C2 - 33522230
AN - SCOPUS:85101433123
SN - 0022-2623
VL - 64
SP - 1510
EP - 1523
JO - Journal of Medicinal Chemistry
JF - Journal of Medicinal Chemistry
IS - 3
ER -