Checkpoint inhibitor promotes tissue repair
Peer-Reviewed Publication
Updates every hour. Last Updated: 14-Dec-2025 13:11 ET (14-Dec-2025 18:11 GMT/UTC)
Immune checkpoint inhibitors are well known as a form of cancer treatment. Researchers at UZH have now identified a new, important function of these inhibitors: promotion of tissue healing. This finding could help advance the treatment of fibrosis and chronic wounds.
In a study published in MedComm - Oncology, researchers report that the enzyme O-GlcNAc Transferase (OGT) plays a key role in driving liver cancer linked to Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD-HCC). The team found that OGT levels increase as the disease progresses. They also discovered that OGT modifies the tumor suppressor protein PTEN in a way that disrupts its normal function, this modification leads to PTEN degradation and reduced phospholipase activity, triggering a cancer-promoting signaling pathway and accelerating tumor growth. The findings suggest that targeting OGT could offer a new therapeutic approach for treating MASLD-related liver cancer.
Abnormal cell proliferation is a major hallmark of cancer. Several proteins are involved in the cell cycle, and most of these regulate the positive or negative control of cyclin-dependent kinases. Previous studies have implicated cell-cycle proteins in regulating immune cells and factors of the tumor immune microenvironment (TIME), highlighting their role in regulating tumor immunity.
Glioblastoma (GBM), a malignant tumor originating from glial, is the most common primary tumor of the central nervous system and the most aggressive form of glioma. Despite surgery, radiation, and chemotherapy, recurrence is almost inevitable, and the five-year survival rate remains around 25%. A major reason for this resilience is the ability of GBM cells to adapt and resist therapy. Epithelial‒mesenchymal transition (EMT), a process in which epithelial cells undergo transformation into cells with a mesenchymal phenotype, has emerged as a central mechanism underlying this adaptability.
Breast cancer (BRCA) remains the most common malignant cancer in women worldwide. Although a range of treatments exists, options with fewer side effects are still limited. SIGLEC15 (sialic acid-binding immunoglobulin-type lectin 15), an emerging immunosuppressive transmembrane protein, is highly expressed across many solid tumors, including BRCA. Understanding its role could help design therapies that overcome the drawbacks of current standards.
Combining an epigenetic therapy with an anti-PD-1 antibody, which uses the body’s natural response to viral infections, showed promising results in patients with relapsed or refractory natural killer/T-cell lymphoma (R/R NKTL), a rare and aggressive cancer with limited treatment options.