Keloid Senescent Fibroblast Elimination & SASP Suppression (Communications Biology, 2025) FOXO4-DRI Induces p53-pS15 Nuclear Exclusion and Apoptosis in Keloid Fibroblast Models A study published in Communications Biology (Nature Publishing Group, 2025) used single-cell RNA sequencing to characterise the senescent cell landscape in keloids pathological scars with tumour-like aggressiveness
Instead, accumulation of infiltrating T cells expressing IFN depleted sensory neurons in patients with anosmia 33
Intrauterine insemination
Key Research Areas for FOXO4-DRI FOXO4p53 protein-protein interaction disruption assays co-immunoprecipitation (CO-IP) and competitive binding studies Senescent cell identification and selective elimination assays SA--galactosidase, p16, p21, p53 staining combined with FOXO4-DRI apoptosis induction p53 TAD2 binding, nuclear exclusion, and mitochondrial translocation studies phospho-p53 (Ser15) pathway research BAX/BCL-2/Caspase-3 intrinsic apoptosis pathway investigations in senescent cell models SASP (Senescence-Associated Secretory Phenotype) characterisation and suppression IL-6, IL-8, MMP, VEGF, CXCL2/3 pathway studies Tissue-specific senescent cell biology fibroblasts, endothelial cells, Leydig cells, chondrocytes, epithelial cells Vascular ageing pathway research endothelial cell senescence, aortic function, and ROS/oxidative stress studies Senescent Leydig cell and male reproductive ageing models FOXO4 nuclear translocation and testosterone synthesis pathway research Chondrocyte senescence and cartilage biology senescent cell removal and chondrogenic potential restoration studies Keloid and pathological scar biology senescent fibroblast elimination and SASP suppression in fibrotic tissue models Senescent cancer cell elimination FOXO4-DRI as a senolytic tool in oncology research models Comparative senolytic research FOXO4-DRI vs
Linkage disequilibrium across the UGT1A locus should not be ignored in association studies of cancer susceptibility
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