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Glucose transporter 1 (GLUT1) expression is associated with intestinal type of gastric carcinoma.

Increased expression of glucose transporter1 (GLUT1) has been reported in many human cancers. We hypothesized that the degree of GLUT1 might provide a useful biological information in gastric adenocarcinoma. RT-PCR and immunostaining were used to analyze GLUT1 expression in gastric cancer. RT-PCR sh...

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Detalles Bibliográficos
Autores principales: Kim, W. S., Kim, Y. Y., Jang, S. J., Kimm, K., Jung, M. H.
Formato: Texto
Lenguaje:English
Publicado: Korean Academy of Medical Sciences 2000
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3054654/
https://www.ncbi.nlm.nih.gov/pubmed/10983690
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author Kim, W. S.
Kim, Y. Y.
Jang, S. J.
Kimm, K.
Jung, M. H.
author_facet Kim, W. S.
Kim, Y. Y.
Jang, S. J.
Kimm, K.
Jung, M. H.
author_sort Kim, W. S.
collection PubMed
description Increased expression of glucose transporter1 (GLUT1) has been reported in many human cancers. We hypothesized that the degree of GLUT1 might provide a useful biological information in gastric adenocarcinoma. RT-PCR and immunostaining were used to analyze GLUT1 expression in gastric cancer. RT-PCR showed GLUT1 expression was not largely detected in normal gastric tissue but was detected in cancerous gastric tissue of counterpart. By immunohistochemistry, GLUT1 protein was absent in normal gastric epithelium and intestinal metaplasia. 11 of 65 patients with gastric adenocarcinoma had specific GLUT1 immunostaining in a plasma membrane pattern with varied intensities. GLUT1 protein did not show any significant correlation with tumor stage and nodal metastasis (p>0.05 by Mann-Whitney test). However, the positive immunostaining for GLUT1 is associated with intestinal differentiation (p=0.003). Our results suggest that GLUT1 protein is associated with intestinal type of gastric cancer.
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spelling pubmed-30546542011-03-15 Glucose transporter 1 (GLUT1) expression is associated with intestinal type of gastric carcinoma. Kim, W. S. Kim, Y. Y. Jang, S. J. Kimm, K. Jung, M. H. J Korean Med Sci Research Article Increased expression of glucose transporter1 (GLUT1) has been reported in many human cancers. We hypothesized that the degree of GLUT1 might provide a useful biological information in gastric adenocarcinoma. RT-PCR and immunostaining were used to analyze GLUT1 expression in gastric cancer. RT-PCR showed GLUT1 expression was not largely detected in normal gastric tissue but was detected in cancerous gastric tissue of counterpart. By immunohistochemistry, GLUT1 protein was absent in normal gastric epithelium and intestinal metaplasia. 11 of 65 patients with gastric adenocarcinoma had specific GLUT1 immunostaining in a plasma membrane pattern with varied intensities. GLUT1 protein did not show any significant correlation with tumor stage and nodal metastasis (p>0.05 by Mann-Whitney test). However, the positive immunostaining for GLUT1 is associated with intestinal differentiation (p=0.003). Our results suggest that GLUT1 protein is associated with intestinal type of gastric cancer. Korean Academy of Medical Sciences 2000-08 /pmc/articles/PMC3054654/ /pubmed/10983690 Text en
spellingShingle Research Article
Kim, W. S.
Kim, Y. Y.
Jang, S. J.
Kimm, K.
Jung, M. H.
Glucose transporter 1 (GLUT1) expression is associated with intestinal type of gastric carcinoma.
title Glucose transporter 1 (GLUT1) expression is associated with intestinal type of gastric carcinoma.
title_full Glucose transporter 1 (GLUT1) expression is associated with intestinal type of gastric carcinoma.
title_fullStr Glucose transporter 1 (GLUT1) expression is associated with intestinal type of gastric carcinoma.
title_full_unstemmed Glucose transporter 1 (GLUT1) expression is associated with intestinal type of gastric carcinoma.
title_short Glucose transporter 1 (GLUT1) expression is associated with intestinal type of gastric carcinoma.
title_sort glucose transporter 1 (glut1) expression is associated with intestinal type of gastric carcinoma.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3054654/
https://www.ncbi.nlm.nih.gov/pubmed/10983690
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