Results 21 to 30 of about 3,728 (186)
Discovery of SKP2-Recruiting PROTACs for Target Protein Degradation. [PDF]
Based on the SKP2‐targeting ligand SL1, we designed non‐covalent PROTACs by linking it with the BRD4 inhibitor JQ1 and the AR antagonist AL through a linker. These PROTACs successfully induced the ubiquitination of BRD4 and AR, followed by proteasome‐mediated degradation.
Dong G +13 more
europepmc +2 more sources
BackgroundBromodomain and extracellular terminal (BET) family (including BRD2, BRD3, and BRD4) is considered to be a major driver of cancer cell growth and a new target for cancer therapy.
Yongli Situ +10 more
doaj +1 more source
Principles of paralog-specific targeted protein degradation engaging the C-degron E3 KLHDC2 [PDF]
PROTAC® (proteolysis-targeting chimera) molecules induce proximity between an E3 ligase and protein-of-interest (POI) to target the POI for ubiquitin-mediated degradation.
Daniel C. Scott +21 more
doaj +2 more sources
Bromodomain and extraterminal domain (BET) proteins are epigenetic readers that regulate gene expression. We investigated whether variants in BET genes are associated with survival outcomes for lung cancer.
Jang Hyuck Lee +17 more
doaj +1 more source
Case report: Immunovirotherapy as a novel add-on treatment in a patient with thoracic NUT carcinoma
NUT carcinoma (NC) is a rare and extremely aggressive form of cancer, usually presenting with intrathoracic or neck manifestations in adolescents and young adults.
Linus D. Kloker +25 more
doaj +1 more source
Bromodomain and Extra-Terminal (BET) Domain Protein Inhibitors for Solid Tumor Cancers [PDF]
The bromodomain and extraterminal (BET) domain protein family is involved in the process of transcription of genetic information. The BET protein family includes BRD2, BRD3, BRD4, and bromodomain testis-specific protein.
Martin V. Nguyen +2 more
doaj +1 more source
BET proteins function as histone code readers of acetylated lysins that determine the positive regulation in transcription of genes involved in cell cycle progression, differentiation, inflammation, and many other pathways. In recent years, thanks to the
Noemi Martella +8 more
doaj +1 more source
NUT-midline carcinoma of the lung with rare BRD3-NUTM1 fusion
Prerana Jha +11 more
doaj +2 more sources

