合成代谢
尿素循环
分解代谢
癌症
尿素
酶
新陈代谢
代谢途径
化学
生物化学
癌细胞
肝癌
生物
氨基酸
精氨酸
遗传学
作者
Rom Keshet,Peter W. Szlosarek,Arkaitz Carracedo,Ayelet Erez
标识
DOI:10.1038/s41568-018-0054-z
摘要
Cancer cells reprogramme metabolism to maximize the use of nitrogen and carbon for the anabolic synthesis of macromolecules that are required during tumour proliferation and growth. To achieve this aim, one strategy is to reduce catabolism and nitrogen disposal. The urea cycle (UC) in the liver is the main metabolic pathway to convert excess nitrogen into disposable urea. Outside the liver, UC enzymes are differentially expressed, enabling the use of nitrogen for the synthesis of UC intermediates that are required to accommodate cellular needs. Interestingly, the expression of UC enzymes is altered in cancer, revealing a revolutionary mechanism to maximize nitrogen incorporation into biomass. In this Review, we discuss the metabolic benefits underlying UC deregulation in cancer and the relevance of these alterations for cancer diagnosis and therapy.
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