NADPH homeostasis in cancer: functions, mechanisms and therapeutic implications.
Huai-Qiang JuJin-Fei LinTian TianDan XieRui-Hua XuPublished in: Signal transduction and targeted therapy (2020)
Nicotinamide adenine dinucleotide phosphate (NADPH) is an essential electron donor in all organisms, and provides the reducing power for anabolic reactions and redox balance. NADPH homeostasis is regulated by varied signaling pathways and several metabolic enzymes that undergo adaptive alteration in cancer cells. The metabolic reprogramming of NADPH renders cancer cells both highly dependent on this metabolic network for antioxidant capacity and more susceptible to oxidative stress. Modulating the unique NADPH homeostasis of cancer cells might be an effective strategy to eliminate these cells. In this review, we summarize the current existing literatures on NADPH homeostasis, including its biological functions, regulatory mechanisms and the corresponding therapeutic interventions in human cancers, providing insights into therapeutic implications of targeting NADPH metabolism and the associated mechanism for cancer therapy.
Keyphrases
- reactive oxygen species
- cancer therapy
- oxidative stress
- induced apoptosis
- signaling pathway
- endothelial cells
- drug delivery
- physical activity
- squamous cell carcinoma
- cell proliferation
- ischemia reperfusion injury
- epithelial mesenchymal transition
- cell death
- childhood cancer
- multidrug resistant
- gram negative
- endoplasmic reticulum stress