Saggese Pasquale, Sellitto Assunta, Martinez Cesar A, Giurato Giorgio, Nassa Giovanni, Rizzo Francesca, Tarallo Roberta, Scafoglio Claudio
Division of Pulmonary and Critical Care Medicine, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA 90095, USA.
Laboratory of Molecular Medicine and Genomics, Department of Medicine, Surgery and Dentistry 'Scuola Medica Salernitana', University of Salerno, 84081 Baronissi (SA), Italy.
Cancers (Basel). 2020 Dec 16;12(12):3788. doi: 10.3390/cancers12123788.
Metabolic reprogramming is a hallmark of cancer, with consistent rewiring of glucose, glutamine, and mitochondrial metabolism. While these metabolic alterations are adequate to meet the metabolic needs of cell growth and proliferation, the changes in critical metabolites have also consequences for the regulation of the cell differentiation state. Cancer evolution is characterized by progression towards a poorly differentiated, stem-like phenotype, and epigenetic modulation of the chromatin structure is an important prerequisite for the maintenance of an undifferentiated state by repression of lineage-specific genes. Epigenetic modifiers depend on intermediates of cellular metabolism both as substrates and as co-factors. Therefore, the metabolic reprogramming that occurs in cancer likely plays an important role in the process of the de-differentiation characteristic of the neoplastic process. Here, we review the epigenetic consequences of metabolic reprogramming in cancer, with particular focus on the role of mitochondrial intermediates and hypoxia in the regulation of cellular de-differentiation. We also discuss therapeutic implications.
代谢重编程是癌症的一个标志,伴随着葡萄糖、谷氨酰胺和线粒体代谢的持续重塑。虽然这些代谢改变足以满足细胞生长和增殖的代谢需求,但关键代谢物的变化也会对细胞分化状态的调节产生影响。癌症演变的特征是朝着低分化、干细胞样表型发展,染色质结构的表观遗传调控是通过抑制谱系特异性基因来维持未分化状态的重要前提。表观遗传修饰因子既依赖细胞代谢中间产物作为底物,也依赖其作为辅助因子。因此,癌症中发生的代谢重编程可能在肿瘤形成过程的去分化过程中发挥重要作用。在这里,我们综述了癌症中代谢重编程的表观遗传后果,特别关注线粒体中间产物和缺氧在细胞去分化调节中的作用。我们还讨论了治疗意义。