磷酸戊糖途径
烟酰胺腺嘌呤二核苷酸磷酸
糖酵解
癌变
代谢途径
NAD+激酶
生物化学
癌细胞
厌氧糖酵解
氧化磷酸化
生物
新陈代谢
烟酰胺腺嘌呤二核苷酸
瓦博格效应
细胞生物学
癌症研究
化学
癌症
酶
氧化酶试验
遗传学
基因
作者
Noorhan Ghanem,Chirine El‐Baba,Khaled Araji,Riyad El‐Khoury,Julnar Usta,Nadine Darwiche
出处
期刊:Chemotherapy
[Karger Publishers]
日期:2021-01-01
卷期号:66 (5-6): 179-191
被引量:54
摘要
<b><i>Background:</i></b> 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. <b><i>Summary:</i></b> 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. <b><i>Key Message:</i></b> Exploiting the metabolic vulnerability of the PPP offers potential novel therapeutic opportunities and improves patients’ response to cancer therapy.
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