Ghanem Noorhan, El-Baba Chirine, Araji Khaled, El-Khoury Riyad, Usta Julnar, Darwiche Nadine
Department of Biochemistry and Molecular Genetics, American University of Beirut, Beirut, Lebanon.
Department of Pathology and Laboratory Medicine, American University of Beirut, Beirut, Lebanon.
Chemotherapy. 2021;66(5-6):179-191. doi: 10.1159/000519784. Epub 2021 Nov 12.
Tumorigenesis is associated with deregulation of nutritional requirements, intermediary metabolites production, and microenvironment interactions. Unlike their normal cell counterparts, tumor cells rely on aerobic glycolysis, through the Warburg effect.
The pentose phosphate pathway (PPP) is a major glucose metabolic shunt that is upregulated in cancer cells. The PPP comprises an oxidative and a nonoxidative phase and is essential for nucleotide synthesis of rapidly dividing cells. The PPP also generates nicotinamide adenine dinucleotide phosphate, which is required for reductive metabolism and to counteract oxidative stress in tumor cells. This article reviews the regulation of the PPP and discusses inhibitors that target its main pathways. Key Message: Exploiting the metabolic vulnerability of the PPP offers potential novel therapeutic opportunities and improves patients' response to cancer therapy.
肿瘤发生与营养需求失调、中间代谢产物生成及微环境相互作用有关。与正常细胞不同,肿瘤细胞通过瓦伯格效应依赖有氧糖酵解。
磷酸戊糖途径(PPP)是癌细胞中上调的主要葡萄糖代谢支路。PPP由氧化阶段和非氧化阶段组成,对快速分裂细胞的核苷酸合成至关重要。PPP还产生烟酰胺腺嘌呤二核苷酸磷酸,这是肿瘤细胞还原代谢和对抗氧化应激所必需的。本文综述了PPP的调控,并讨论了靶向其主要途径的抑制剂。关键信息:利用PPP的代谢脆弱性提供了潜在的新型治疗机会,并改善了患者对癌症治疗的反应。