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Prolyl hydroxylase domain enzymes and their role in cell signaling and cancer metabolism
Institution:1. Department of Clinical Laboratory, Children''s Hospital of Nanjing Medical University, Nanjing 210008, China;2. Department of Nephrology, Children''s Hospital of Nanjing Medical University, 72 Guangzhou Road, Nanjing 210008, China;3. Jiangsu Key Laboratory of Pediatrics, Nanjing Medical University, Nanjing 210029, China;4. Nanjing Key Laboratory of Pediatrics, Children''s Hospital of Nanjing Medical University, Nanjing 210008, China
Abstract:The prolyl hydroxylase domain (PHD) enzymes regulate the stability of the hypoxia-inducible factor (HIF) in response to oxygen availability. During oxygen limitation, the inhibition of PHD permits the stabilization of HIF, allowing the cellular adaptation to hypoxia. This adaptation is especially important for solid tumors, which are often exposed to a hypoxic environment. However, and despite their original role as the oxygen sensors of the cell, PHD are currently known to display HIF-independent and hydroxylase-independent functions in the control of different cellular pathways, including mTOR pathway, NF-kB pathway, apoptosis and cellular metabolism. In this review, we summarize the recent advances in the regulation and functions of PHD in cancer signaling and cell metabolism.
Keywords:2-Oxoglutarate  Cancer  Metabolism  mTOR  PHD
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