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本文引用的文献

1
Expression of the GLUT1 glucose transporter and p53 in carcinomas of the pancreatobiliary tract.GLUT1 葡萄糖转运蛋白和 p53 在胰胆管癌中的表达。
Pathol Res Pract. 2010 Jan 15;206(1):24-9. doi: 10.1016/j.prp.2009.07.018. Epub 2009 Oct 12.
2
Facilitative glucose transporter 9 expression affects glucose sensing in pancreatic beta-cells.易化葡萄糖转运蛋白 9 的表达会影响胰腺β细胞的葡萄糖感应。
Endocrinology. 2009 Dec;150(12):5302-10. doi: 10.1210/en.2009-0747. Epub 2009 Oct 6.
3
Facilitative glucose transporter 9, a unique hexose and urate transporter.易化葡萄糖转运蛋白 9,一种独特的己糖和尿酸转运蛋白。
Am J Physiol Endocrinol Metab. 2009 Oct;297(4):E831-5. doi: 10.1152/ajpendo.00296.2009.
4
Glut9 is a major regulator of urate homeostasis and its genetic inactivation induces hyperuricosuria and urate nephropathy.Glut9是尿酸盐稳态的主要调节因子,其基因失活会导致高尿酸尿症和尿酸盐肾病。
Proc Natl Acad Sci U S A. 2009 Sep 8;106(36):15501-6. doi: 10.1073/pnas.0904411106. Epub 2009 Aug 21.
5
Glucose deprivation contributes to the development of KRAS pathway mutations in tumor cells.葡萄糖剥夺促进肿瘤细胞中KRAS信号通路突变的发生。
Science. 2009 Sep 18;325(5947):1555-9. doi: 10.1126/science.1174229. Epub 2009 Aug 6.
6
Evaluation of expression and function of the H+/myo-inositol transporter HMIT.H⁺/肌醇转运体HMIT的表达及功能评估
BMC Cell Biol. 2009 Jul 16;10:54. doi: 10.1186/1471-2121-10-54.
7
Insulin-stimulated translocation of glucose transporter (GLUT) 12 parallels that of GLUT4 in normal muscle.在正常肌肉中,胰岛素刺激的葡萄糖转运蛋白12(GLUT12)易位与葡萄糖转运蛋白4(GLUT4)的易位相似。
J Clin Endocrinol Metab. 2009 Sep;94(9):3535-42. doi: 10.1210/jc.2009-0162. Epub 2009 Jun 23.
8
Erythroid glucose transporters.红细胞葡萄糖转运蛋白
Curr Opin Hematol. 2009 May;16(3):165-72. doi: 10.1097/MOH.0b013e328329905c.
9
Growth inhibition of head and neck carcinomas by D-allose.D-阿洛酮糖对头颈部癌的生长抑制作用
Head Neck. 2009 Aug;31(8):1049-55. doi: 10.1002/hed.21070.
10
GLUT8, the enigmatic intracellular hexose transporter.GLUT8,神秘的细胞内己糖转运蛋白。
Am J Physiol Endocrinol Metab. 2009 Apr;296(4):E614-8. doi: 10.1152/ajpendo.91019.2008. Epub 2009 Jan 27.

糖转运蛋白在癌症中的潜在作用及其与抗癌治疗的关系。

Potential role of sugar transporters in cancer and their relationship with anticancer therapy.

机构信息

Biomedical Research Institute, A Coruña University Hospital, As Xubias 84, 15006 A Coruña, Spain.

出版信息

Int J Endocrinol. 2010;2010. doi: 10.1155/2010/205357. Epub 2010 Jul 18.

DOI:10.1155/2010/205357
PMID:20706540
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2913528/
Abstract

Sugars, primarily glucose and fructose, are the main energy source of cells. Because of their hydrophilic nature, cells use a number of transporter proteins to introduce sugars through their plasma membrane. Cancer cells are well known to display an enhanced sugar uptake and consumption. In fact, sugar transporters are deregulated in cancer cells so they incorporate higher amounts of sugar than normal cells. In this paper, we compile the most significant data available about biochemical and biological properties of sugar transporters in normal tissues and we review the available information about sugar carrier expression in different types of cancer. Moreover, we describe the possible pharmacological interactions between drugs currently used in anticancer therapy and the expression or function of facilitative sugar transporters. Finally, we also go into the insights about the future design of drugs targeted against sugar utilization in cancer cells.

摘要

糖,主要是葡萄糖和果糖,是细胞的主要能量来源。由于其亲水性,细胞使用许多转运蛋白将糖通过质膜导入细胞内。众所周知,癌细胞具有增强的糖摄取和消耗能力。事实上,癌细胞中的糖转运蛋白失调,因此它们摄取的糖比正常细胞多。在本文中,我们汇总了关于正常组织中糖转运蛋白的生化和生物学特性的最有意义的数据,并综述了不同类型癌症中糖载体表达的现有信息。此外,我们还描述了目前用于癌症治疗的药物与促进性糖转运蛋白的表达或功能之间可能存在的药理相互作用。最后,我们还探讨了针对癌细胞中糖利用的药物设计的未来思路。