Literature DB >> 28042452

Anticancer agents interacting with membrane glucose transporters.

C Granchi1, S Fortunato1, F Minutolo1.   

Abstract

The altered metabolism observed in cancer cells generally consists in increased glucose uptake and glycolytic activity. This is associated with an overexpression of glucose transporter proteins (GLUTs), which facilitate glucose uptake across the plasma membrane and play a crucial role in the survival of cancer cells. Therefore GLUTs are considered as suitable targets for the treatment of cancer. Herein we review some of the most relevant GLUT inhibitors that have been recently developed as prospective anticancer agents.

Entities:  

Year:  2016        PMID: 28042452      PMCID: PMC5198910          DOI: 10.1039/C6MD00287K

Source DB:  PubMed          Journal:  Medchemcomm        ISSN: 2040-2503            Impact factor:   3.597


  96 in total

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7.  Hexose transporter GLUT1 harbors several distinct regulatory binding sites for flavones and tyrphostins.

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Journal:  Biochemistry       Date:  2011-09-27       Impact factor: 3.162

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10.  Myricetin, quercetin and catechin-gallate inhibit glucose uptake in isolated rat adipocytes.

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Journal:  Biochem J       Date:  2005-03-15       Impact factor: 3.857

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  23 in total

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2.  Transmembrane Exchange of Fluorosugars: Characterization of Red Cell GLUT1 Kinetics Using 19F NMR.

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5.  Aromatic carbohydrate amphiphile disrupts cancer spheroids and prevents relapse.

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Review 6.  Power of two: combination of therapeutic approaches involving glucose transporter (GLUT) inhibitors to combat cancer.

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Review 7.  Plant-derived glucose transport inhibitors with potential antitumor activity.

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10.  Targeting of GLUT5 for Transporter-Mediated Drug-Delivery Is Contingent upon Substrate Hydrophilicity.

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