Re-oxygenation Causes Hypoxic Tumor Regression Through Restoration of p53 Wild-Type Conformation and Post-Translational Modifications
This 2012 study explored how re-oxygenation impacts hypoxic tumors by restoring wild-type functionality to p53, a key tumor suppressor often rendered inactive under low oxygen conditions. Under hypoxia, p53 assumes a mutant-like conformation that diminishes its transcriptional and tumor-suppressive activities. Re-oxygenation with 30% oxygen at normobaric pressure reversed these effects