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Inhibition of cell proliferation and glucose uptake in human laryngeal carcinoma cells by antisense oligonucleotides against glucose transporter-1

✍ Scribed by Shui-Hong Zhou; Jun Fan; Xiao-Ming Chen; Ke-Jia Cheng; Shen-Qing Wang


Publisher
John Wiley and Sons
Year
2009
Tongue
English
Weight
464 KB
Volume
31
Category
Article
ISSN
1043-3074

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✦ Synopsis


Abstract

Background.

Malignant cells show increased glucose uptake in vitro and in vivo, which is thought to be mediated by glucose transporters. In this study, we investigated the effect of plasmid‐derived antisense RNA against the Glut‐l gene on proliferation and glucose uptake in laryngeal carcinoma Hep‐2 cells.

Methods.

The expression plasmids pcDNA3.1(+)‐Glut‐1 and pcDNA3.1(+)‐anti Glut‐1 were constructed. The MTT method was used to assess cell growth inhibition. The expression of Glut‐1 mRNA and protein was detected by reverse transcriptase‐polymerase chain reaction and Western blotting, respectively.

Results.

After transfection, Glut‐1 AS clearly inhibited glucose uptake and cell growth in Hep‐2 cells, and we observed a decrease in the expression of Glut‐1 mRNA and protein in Hep‐2 cells.

Conclusions.

Glut‐1 AS decreases glucose uptake and inhibits the proliferation of Hep‐2 cells. © 2009 Wiley Periodicals, Inc. Head Neck, 2009


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## Abstract In recent years, successful examples of antisense oligonucleotide (AS) therapy for genetic diseases have stimulated scientists to investigate its application on cancer diseases. AS can be used to down‐regulate the mRNA and protein expression by annealing to specific region of the target