TY - JOUR
T1 - Specific non-genetic IAP-based protein erasers (SNIPERs) as a potential therapeutic strategy
AU - Ma, Zonghui
AU - Ji, Yu
AU - Yu, Yifan
AU - Liang, Dailin
N1 - Publisher Copyright:
© 2021 Elsevier Masson SAS
PY - 2021/4/15
Y1 - 2021/4/15
N2 - As a newly emerged technology, PROTAC (proteolysis targeting chimera) is a promising therapeutic strategy for varieties of diseases. Unlike small molecule inhibitors, PROTACs catalytically induce target proteins degradation, including currently “undruggable” target proteins. In addition, PROTACs can be a potentially successful strategy to overcome drug resistance. IAPs can inhibit apoptosis by inhibiting caspase, and also exhibits the activity of E3 ubiquitin ligase. Specific and nongenetic IAP-based protein erasers (SNIPERs) are hybrid molecules that designed based on IAPs, and used to degrade the target proteins closely associated with diseases. Their structures consist of three parts, including target protein ligand, E3 ligase ligand and the linker between them. SNIPERs (PROTACs) degrade diseases-associated proteins through human inherent ubiquitin-proteasome system. So far, many SNIPERs have been developed to treat diseases that difficult to handle by traditional methods, such as radiotherapy, chemotherapy and small molecule inhibitors, and showed promising prospects in application. In this paper, the recent advances of SNIPERs were summarized, and the chances and challenges associated with this area were also highlighted.
AB - As a newly emerged technology, PROTAC (proteolysis targeting chimera) is a promising therapeutic strategy for varieties of diseases. Unlike small molecule inhibitors, PROTACs catalytically induce target proteins degradation, including currently “undruggable” target proteins. In addition, PROTACs can be a potentially successful strategy to overcome drug resistance. IAPs can inhibit apoptosis by inhibiting caspase, and also exhibits the activity of E3 ubiquitin ligase. Specific and nongenetic IAP-based protein erasers (SNIPERs) are hybrid molecules that designed based on IAPs, and used to degrade the target proteins closely associated with diseases. Their structures consist of three parts, including target protein ligand, E3 ligase ligand and the linker between them. SNIPERs (PROTACs) degrade diseases-associated proteins through human inherent ubiquitin-proteasome system. So far, many SNIPERs have been developed to treat diseases that difficult to handle by traditional methods, such as radiotherapy, chemotherapy and small molecule inhibitors, and showed promising prospects in application. In this paper, the recent advances of SNIPERs were summarized, and the chances and challenges associated with this area were also highlighted.
KW - Antitumor
KW - IAPs
KW - PROTAC
KW - Protein degradation
KW - SNIPER
KW - Ubiquitin-proteasome system (UPS)
UR - http://www.scopus.com/inward/record.url?scp=85101656896&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85101656896&partnerID=8YFLogxK
U2 - 10.1016/j.ejmech.2021.113247
DO - 10.1016/j.ejmech.2021.113247
M3 - Review article
C2 - 33652355
AN - SCOPUS:85101656896
SN - 0223-5234
VL - 216
JO - European journal of medicinal chemistry
JF - European journal of medicinal chemistry
M1 - 113247
ER -