Lauria Graziantonio, Curcio Rosita, Lunetti Paola, Tiziani Stefano, Coppola Vincenzo, Dolce Vincenza, Fiermonte Giuseppe, Ahmed Amer
Department of Pharmacy, Health and Nutritional Sciences, University of Calabria, 87036 Rende, Italy.
Department of Bioscience, Biotechnology and Environment, University of Bari, 70125 Bari, Italy.
Cancers (Basel). 2023 Jan 8;15(2):411. doi: 10.3390/cancers15020411.
Pancreatic cancer is among the deadliest cancers worldwide and commonly presents as pancreatic ductal adenocarcinoma (PDAC). Metabolic reprogramming is a hallmark of PDAC. Glucose and glutamine metabolism are extensively rewired in order to fulfil both energetic and synthetic demands of this aggressive tumour and maintain favorable redox homeostasis. The mitochondrial pyruvate carrier (MPC), the glutamine carrier (SLC1A5_Var), the glutamate carrier (GC), the aspartate/glutamate carrier (AGC), and the uncoupling protein 2 (UCP2) have all been shown to influence PDAC cell growth and progression. The expression of MPC is downregulated in PDAC and its overexpression reduces cell growth rate, whereas the other four transporters are usually overexpressed and the loss of one or more of them renders PDAC cells unable to grow and proliferate by altering the levels of crucial metabolites such as aspartate. The aim of this review is to comprehensively evaluate the current experimental evidence about the function of these carriers in PDAC metabolic rewiring. Dissecting the precise role of these transporters in the context of the tumour microenvironment is necessary for targeted drug development.
胰腺癌是全球最致命的癌症之一,通常表现为胰腺导管腺癌(PDAC)。代谢重编程是PDAC的一个标志。葡萄糖和谷氨酰胺代谢被广泛重塑,以满足这种侵袭性肿瘤的能量和合成需求,并维持良好的氧化还原稳态。线粒体丙酮酸载体(MPC)、谷氨酰胺载体(SLC1A5_Var)、谷氨酸载体(GC)、天冬氨酸/谷氨酸载体(AGC)和解偶联蛋白2(UCP2)均已被证明会影响PDAC细胞的生长和进展。MPC的表达在PDAC中下调,其过表达会降低细胞生长速率,而其他四种转运蛋白通常过表达,其中一种或多种的缺失会通过改变关键代谢物(如天冬氨酸)的水平,使PDAC细胞无法生长和增殖。本综述的目的是全面评估目前关于这些载体在PDAC代谢重塑中功能的实验证据。剖析这些转运蛋白在肿瘤微环境中的精确作用对于靶向药物开发是必要的。