Department of Neuroscience and Center for Neurovirology, Temple University School of Medicine, Philadelphia, Pennsylvania, United States of America.
PLoS One. 2012;7(4):e35054. doi: 10.1371/journal.pone.0035054. Epub 2012 Apr 9.
Recent studies have reported the detection of the human neurotropic virus, JCV, in a significant population of brain tumors, including medulloblastomas. Accordingly, expression of the JCV early protein, T-antigen, which has transforming activity in cell culture and in transgenic mice, results in the development of a broad range of tumors of neural crest and glial origin. Evidently, the association of T-antigen with a range of tumor-suppressor proteins, including p53 and pRb, and signaling molecules, such as β-catenin and IRS-1, plays a role in the oncogenic function of JCV T-antigen. We demonstrate that T-antigen expression is suppressed by glucose deprivation in medulloblastoma cells and in glioblastoma xenografts that both endogenously express T-antigen. Mechanistic studies indicate that glucose deprivation-mediated suppression of T-antigen is partly influenced by 5'-activated AMP kinase (AMPK), an important sensor of the AMP/ATP ratio in cells. In addition, glucose deprivation-induced cell cycle arrest in the G1 phase is blocked with AMPK inhibition, which also prevents T-antigen downregulation. Furthermore, T-antigen prevents G1 arrest and sustains cells in the G2 phase during glucose deprivation. On a functional level, T-antigen downregulation is partially dependent on reactive oxygen species (ROS) production during glucose deprivation, and T-antigen prevents ROS induction, loss of ATP production, and cytotoxicity induced by glucose deprivation. Additionally, we have found that T-antigen is downregulated by the glycolytic inhibitor, 2-deoxy-D-glucose (2-DG), and the pentose phosphate inhibitors, 6-aminonicotinamide and oxythiamine, and that T-antigen modulates expression of the glycolytic enzyme, hexokinase 2 (HK2), and the pentose phosphate enzyme, transaldolase-1 (TALDO1), indicating a potential link between T-antigen and metabolic regulation. These studies point to the possible involvement of JCV T-antigen in medulloblastoma proliferation and the metabolic phenotype and may enhance our understanding of the role of viral proteins in glycolytic tumor metabolism, thus providing useful targets for the treatment of virus-induced tumors.
最近的研究报告称,在包括成神经管细胞瘤在内的大量脑肿瘤中检测到了人类神经嗜性病毒 JCV。因此,JCV 早期蛋白 T 抗原的表达具有转化细胞培养和转基因小鼠的活性,导致神经嵴和神经胶质来源的广泛肿瘤的发展。显然,T 抗原与一系列肿瘤抑制蛋白,包括 p53 和 pRb,以及信号分子,如 β-连环蛋白和 IRS-1 的关联,在 JCV T 抗原的致癌功能中发挥作用。我们证明 T 抗原的表达在成神经管细胞瘤细胞和内源性表达 T 抗原的神经胶质瘤异种移植中受到葡萄糖剥夺的抑制。机制研究表明,葡萄糖剥夺介导的 T 抗原抑制部分受 5'-激活的 AMP 激酶 (AMPK) 的影响,AMPK 是细胞中 AMP/ATP 比值的重要传感器。此外,用 AMPK 抑制剂阻断葡萄糖剥夺诱导的细胞周期 G1 期阻滞,也阻止了 T 抗原下调。此外,T 抗原在葡萄糖剥夺期间阻止 G1 期阻滞并使细胞维持在 G2 期。在功能水平上,T 抗原的下调部分依赖于葡萄糖剥夺期间的活性氧 (ROS) 的产生,并且 T 抗原可以防止 ROS 诱导、ATP 产生丧失以及葡萄糖剥夺引起的细胞毒性。此外,我们发现 T 抗原可被糖酵解抑制剂 2-脱氧-D-葡萄糖 (2-DG) 和戊糖磷酸抑制剂 6-氨基烟酰胺和噻唑啉-1 下调,并且 T 抗原调节糖酵解酶己糖激酶 2 (HK2) 和戊糖磷酸酶转醛酶-1 (TALDO1) 的表达,表明 T 抗原与代谢调节之间可能存在潜在联系。这些研究表明 JCV T 抗原可能参与成神经管细胞瘤的增殖和代谢表型,并可能增强我们对病毒蛋白在糖酵解肿瘤代谢中的作用的理解,从而为治疗病毒诱导的肿瘤提供有用的靶点。