Inserm U 1035, BMGIC, 33076 Bordeaux, France; Université de Bordeaux, 146 rue Léo Saignat, 33076 Bordeaux, France.
Service de Biochimie Métabolique, CHU de Bordeaux, France; Inserm U1211 Maladies Rares: Génétique et Métabolisme (MRGM), Université de Bordeaux, Bordeaux, France.
Cell Rep. 2018 Jun 19;23(12):3621-3634. doi: 10.1016/j.celrep.2018.05.060.
Although growing evidence indicates that bioenergetic metabolism plays an important role in the progression of tumorigenesis, little information is available on the contribution of reprogramming of energy metabolism in cancer initiation. By applying a quantitative proteomic approach and targeted metabolomics, we find that specific metabolic modifications precede primary skin tumor formation. Using a multistage model of ultraviolet B (UVB) radiation-induced skin cancer, we show that glycolysis, tricarboxylic acid (TCA) cycle, and fatty acid β-oxidation are decreased at a very early stage of photocarcinogenesis, while the distal part of the electron transport chain (ETC) is upregulated. Reductive glutamine metabolism and the activity of dihydroorotate dehydrogenase (DHODH) are both necessary for maintaining high ETC. Mice with decreased DHODH activity or impaired ETC failed to develop pre-malignant and malignant lesions. DHODH activity represents a major link between DNA repair efficiency and bioenergetic patterning during skin carcinogenesis.
尽管越来越多的证据表明生物能量代谢在肿瘤发生的发展中起着重要作用,但关于能量代谢重编程在癌症起始中的作用的信息却很少。通过应用定量蛋白质组学方法和靶向代谢组学,我们发现特定的代谢修饰先于原发性皮肤肿瘤的形成。通过紫外线 B(UVB)辐射诱导的皮肤癌多阶段模型,我们表明糖酵解、三羧酸(TCA)循环和脂肪酸β氧化在光致癌发生的早期阶段就降低了,而电子传递链(ETC)的远端部分被上调。还原性谷氨酰胺代谢和二氢乳清酸脱氢酶(DHODH)的活性对于维持高 ETC 都是必需的。DHODH 活性降低或 ETC 受损的小鼠无法形成恶性前病变和恶性病变。DHODH 活性代表了皮肤癌变过程中 DNA 修复效率和生物能量模式之间的主要联系。