This review systematically integrates advances in STAMBPL1 biology from structural to translational studies, highlighting its promise as a therapeutic target for precision cancer therapy.
Prostate cancer (PC) is one of the most common male cancers. Cancer cells are well known for their capacity to avoid programed cell death (PCD) via a variety of molecular pathways, allowing them to survive oncogenic stress and therapeutic challenges. Although oncogenic splicing factors are frequently dysregulated in tu...
DUBs function as central signaling hubs orchestrating malignant progression, treatment resistance, and immune evasion in breast cancer, positioning them as promising prognostic biomarkers and therapeutic targets.
Xiao-Yu Zhang, Dun-Ya Yang, Xiang-Wu Lin et al.· Discover Oncology· 0 citations
Receptor-interacting protein kinase 1 (RIPK1) mediates cell survival, inflammation, and cell death, and its kinase-independent scaffolding function drives tumor progression and therapeutic resistance, which cannot be eliminated by conventional RIPK1 kinase inhibitors. To overcome this limitation, we adopted proteolysis...
Shun-Xin Guo, Ming-Ze Tang, Pei Yu et al.· European journal of medicina...· 0 citations
S-phase kinase-associated protein 2 (SKP2), a key substrate-recognition subunit of the Skp1-Cul1-F-box (SCF) E3 ubiquitin ligase complex, promotes the ubiquitin–proteasome-mediated degradation of tumor suppressors such as p27Kip1 and p21(Cip1/Waf1). Through these activities, SKP2 regulates critical cellular processes,...
Yue-Ying Zhang, O. Faruq, M. Shrestha et al.· Cells· 0 citations
The ubiquitin-specific peptidase 42 (USP42) is a cysteine-dependent deubiquitinase with pro-tumorigenic roles in several cancers. In lung adenocarcinoma (LUAD), elevated USP42 expression correlates with advanced stage and poor survival, mirroring the prognostic impact of prostaglandin-endoperoxide synthase 2 (PTGS2) ov...
Hai-Nan Ye, Ji Shen, Dan Liu et al.· Journal of Molecular Histolo...· 0 citations
It is proposed that UBA1 functions as a proteostasis-innate immunity checkpoint whose biological output is determined by residual enzymatic activity, subcellular distribution, lineage context, and clone size and suggests a mechanism-based approach to therapeutic intervention in VEXAS syndrome and malignancy.
Yan-Yu Zhang, Quan-Xin Su· Frontiers in Immunology· 0 citations
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