Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
J Hepatol. 2022 Sep;77(3):849-864. doi: 10.1016/j.jhep.2022.04.038. Epub 2022 May 18.
Metabolic reprogramming is a hallmark of cancer and allows tumour cells to meet the increased energy demands required for rapid proliferation, invasion, and metastasis. Indeed, many tumour cells acquire distinctive metabolic and bioenergetic features that enable them to survive in resource-limited conditions, mainly by harnessing alternative nutrients. Several recent studies have explored the metabolic plasticity of cancer cells with the aim of identifying new druggable targets, while therapeutic strategies to limit the access to nutrients have been successfully applied to the treatment of some tumours. Cholangiocarcinoma (CCA), a highly heterogeneous tumour, is the second most common form of primary liver cancer. It is characterised by resistance to chemotherapy and poor prognosis, with 5-year survival rates of below 20%. Deregulation of metabolic pathways have been described during the onset and progression of CCA. Increased aerobic glycolysis and glutamine anaplerosis provide CCA cells with the ability to generate biosynthetic intermediates. Other metabolic alterations involving carbohydrates, amino acids and lipids have been shown to sustain cancer cell growth and dissemination. In this review, we discuss the complex metabolic rewiring that occurs during CCA development and leads to unique nutrient addiction. The possible role of therapeutic interventions based on metabolic changes is also thoroughly discussed.
代谢重编程是癌症的一个标志,它使肿瘤细胞能够满足快速增殖、侵袭和转移所需的增加的能量需求。事实上,许多肿瘤细胞获得了独特的代谢和生物能量特征,使它们能够在资源有限的条件下生存,主要是通过利用替代营养物质。最近的几项研究探讨了癌细胞的代谢可塑性,旨在确定新的可药物治疗的靶点,而限制营养物质获取的治疗策略已成功应用于某些肿瘤的治疗。胆管癌(CCA)是一种高度异质性的肿瘤,是原发性肝癌的第二大常见形式。它的特点是对化疗的耐药性和预后不良,5 年生存率低于 20%。在 CCA 的发生和进展过程中,已经描述了代谢途径的失调。有氧糖酵解和谷氨酰胺回补的增加使 CCA 细胞能够生成生物合成中间体。其他涉及碳水化合物、氨基酸和脂质的代谢改变被证明可以维持癌细胞的生长和扩散。在这篇综述中,我们讨论了在 CCA 发展过程中发生的复杂代谢重编程,导致了独特的营养成瘾。还彻底讨论了基于代谢变化的治疗干预的可能作用。