
Frontiers in Immunology, Journal Year: 2025, Volume and Issue: 16
Published: March 27, 2025
The review by Yongmei Wang et al., "The ubiquitin-proteasome system in the tumor immune microenvironment: a key force combination therapy," provides comprehensive analysis of UPS's role TIME, highlighting its potential as therapeutic target immunotherapy [1]. Despite this, could benefit from more detailed discussion on impact transcription factor FOXP3, regulation cell function E3 ubiquitin-protein ligases, and emerging Proteolysis Targeting Chimeras (PROTACs) modulating ligase activity. FOXP3 stability [2].The activity expression are regulated various such CBLB STUB1. These mechanisms should be elaborated upon to provide understanding how UPS influences Treg biology [7].Identifying ligases their cancers like breast cancer can new targets for patients, especially those with advanced, recurrent, metastatic disease [8].In terms drug development, there has been significant progress targeting therapy. Proteasome inhibitors, bortezomib, have approved treatment multiple myeloma mantle lymphoma [9]. Additionally, development deubiquitinating enzyme (DUB) inhibitors is an area research, several compounds entering preclinical clinical trials [10]. For instance, USP7 inhibitor P5091 shown promise promoting ubiquitination degradation MDM2, thereby activating p53 pathway [11].The also thorough summary current research targets. SPOP FBXO22, ubiquitinate degrade PD -L1, suggesting that inhibition enhance anti-tumor responses [11]. Furthermore, neddylation regulating CRL complexes highlighted, disrupt TAM recruitment evasion .Proteolysis i s promising strategy [12], one end protein interest (POI) other binding ubiquitin ligase. By
Language: Английский