Facilitative glucose transporters: Implications for cancer detection, prognosis and treatment

被引:425
作者
Barron, Carly C. [1 ]
Bilan, Philip J. [2 ]
Tsakiridis, Theodoros [3 ,4 ]
Tsiani, Evangelia [1 ]
机构
[1] Brock Univ, Dept Hlth Sci, St Catharines, ON L2S 3A1, Canada
[2] Hosp Sick Children, Peter Gilgan Ctr Res & Learning, Cell Biol Program, Toronto, ON M5G 0A4, Canada
[3] McMaster Univ, Dept Oncol, Hamilton, ON L8S 4L8, Canada
[4] McMaster Univ, Dept Pathol & Mol Med, Hamilton, ON L8S 4L8, Canada
来源
METABOLISM-CLINICAL AND EXPERIMENTAL | 2016年 / 65卷 / 02期
基金
加拿大自然科学与工程研究理事会;
关键词
Glucose transporter; GLUT; SLC2; Warburg effect; Cancer metabolism; POSITRON-EMISSION-TOMOGRAPHY; CELL LUNG-CANCER; HYPOXIA-INDUCIBLE FACTOR-1-ALPHA; MYO-INOSITOL SYMPORTER; GENE-EXPRESSION; FRUCTOSE TRANSPORTER; BREAST-CANCER; DIFFERENTIAL EXPRESSION; TISSUE DISTRIBUTION; BLADDER-CANCER;
D O I
10.1016/j.metabol.2015.10.007
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
It is long recognized that cancer cells display increased glucose uptake and metabolism. In a rate-limiting step for glucose metabolism, the glucose transporter (GLUT) proteins facilitate glucose uptake across the plasma membrane. Fourteen members of the GLUT protein family have been identified in humans. This review describes the major characteristics of each member of the GLUT family and highlights evidence of abnormal expression in tumors and cancer cells. The regulation of GLUTs by key proliferation and pro-survival pathways including the phosphatidylinositol 3-kinase (PI3K)-Akt, hypoxia-inducible factor-1 (HIF-1), Ras, c-Myc and p53 pathways is discussed. The clinical utility of GLUT expression in cancer has been recognized and evidence regarding the use of GLUTs as prognostic or predictive biomarkers is presented. GLUTs represent attractive targets for cancer therapy and this review summarizes recent studies in which GLUT1, GLUT3, GLUTS and others are inhibited to decrease cancer growth. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:124 / 139
页数:16
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