Markouli Mariam, Strepkos Dimitrios, Papavassiliou Kostas A, Papavassiliou Athanasios G, Piperi Christina
Department of Biological Chemistry, Medical School, National and Kapodistrian University of Athens, 11527 Athens, Greece.
Cancers (Basel). 2022 May 27;14(11):2655. doi: 10.3390/cancers14112655.
Metabolic alterations in neoplastic cells have recently gained increasing attention as a main topic of research, playing a crucial regulatory role in the development and progression of tumors. The interplay between epigenetic modifications and metabolic pathways in glioblastoma cells has emerged as a key pathogenic area with great potential for targeted therapy. Epigenetic mechanisms have been demonstrated to affect main metabolic pathways, such as glycolysis, pentose phosphate pathway, gluconeogenesis, oxidative phosphorylation, TCA cycle, lipid, and glutamine metabolism by modifying key regulatory genes. Although epigenetic modifications can primarily promote the activity of metabolic pathways, they may also exert an inhibitory role. In this way, they participate in a complex network of interactions that regulate the metabolic behavior of malignant cells, increasing their heterogeneity and plasticity. Herein, we discuss the main epigenetic mechanisms that regulate the metabolic pathways in glioblastoma cells and highlight their targeting potential against tumor progression.
肿瘤细胞中的代谢改变作为一个主要研究课题,近来受到越来越多的关注,在肿瘤的发生和发展中起着关键的调节作用。胶质母细胞瘤细胞中表观遗传修饰与代谢途径之间的相互作用已成为一个具有巨大靶向治疗潜力的关键致病领域。表观遗传机制已被证明可通过修饰关键调控基因来影响主要代谢途径,如糖酵解、磷酸戊糖途径、糖异生、氧化磷酸化、三羧酸循环、脂质和谷氨酰胺代谢。虽然表观遗传修饰主要可促进代谢途径的活性,但它们也可能发挥抑制作用。通过这种方式,它们参与了一个复杂的相互作用网络,调节恶性细胞的代谢行为,增加其异质性和可塑性。在此,我们讨论调节胶质母细胞瘤细胞代谢途径的主要表观遗传机制,并强调它们针对肿瘤进展的靶向潜力。