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METHYLATION STATUS OF EPIDERMAL GROWTH FACTOR RECEPTOR GENE IN LUNG CARCINOMA CELLS

The methylation status of the epidermal growth factor receptor (EGFR) gene was compared in cell lines from four major types of lung carcinoma, small cell lung carcinoma (SCLC), large cell lung carcinoma, squamous cell carcinoma and adenocarcinoma, in order to examine whether DNA methylation is respo...

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Detalles Bibliográficos
Autores principales: Gamou, Shinobu, Shimosato, Yukio, Merlino, Glenn T., Shimizu, Nobuyoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1988
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5917620/
https://www.ncbi.nlm.nih.gov/pubmed/2848004
http://dx.doi.org/10.1111/j.1349-7006.1988.tb00065.x
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author Gamou, Shinobu
Shimosato, Yukio
Merlino, Glenn T.
Shimizu, Nobuyoshi
author_facet Gamou, Shinobu
Shimosato, Yukio
Merlino, Glenn T.
Shimizu, Nobuyoshi
author_sort Gamou, Shinobu
collection PubMed
description The methylation status of the epidermal growth factor receptor (EGFR) gene was compared in cell lines from four major types of lung carcinoma, small cell lung carcinoma (SCLC), large cell lung carcinoma, squamous cell carcinoma and adenocarcinoma, in order to examine whether DNA methylation is responsible for the suppression of EGFR gene in SCLC cells. Southern blot analysis revealed that the structural region of the EGFR gene is methylated to various degrees regardless of the expression of EGF receptor on the surface. An 8‐kilobase EcoRI fragment which contains the EGFR gene promoter region is readily digested with various methylation‐sensitive restriction enzymes in all types of cells, indicating that the EGFR gene 5’region is barely methylated. Thus, a mechanism other than DNA methylation appears to control EGFR gene expression and the lack of EGFR gene expression in SCLC cells may be caused by a paucity of some transcription regulatory factor(s).
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spelling pubmed-59176202018-05-11 METHYLATION STATUS OF EPIDERMAL GROWTH FACTOR RECEPTOR GENE IN LUNG CARCINOMA CELLS Gamou, Shinobu Shimosato, Yukio Merlino, Glenn T. Shimizu, Nobuyoshi Jpn J Cancer Res Rapid Communication The methylation status of the epidermal growth factor receptor (EGFR) gene was compared in cell lines from four major types of lung carcinoma, small cell lung carcinoma (SCLC), large cell lung carcinoma, squamous cell carcinoma and adenocarcinoma, in order to examine whether DNA methylation is responsible for the suppression of EGFR gene in SCLC cells. Southern blot analysis revealed that the structural region of the EGFR gene is methylated to various degrees regardless of the expression of EGF receptor on the surface. An 8‐kilobase EcoRI fragment which contains the EGFR gene promoter region is readily digested with various methylation‐sensitive restriction enzymes in all types of cells, indicating that the EGFR gene 5’region is barely methylated. Thus, a mechanism other than DNA methylation appears to control EGFR gene expression and the lack of EGFR gene expression in SCLC cells may be caused by a paucity of some transcription regulatory factor(s). Blackwell Publishing Ltd 1988-09 /pmc/articles/PMC5917620/ /pubmed/2848004 http://dx.doi.org/10.1111/j.1349-7006.1988.tb00065.x Text en
spellingShingle Rapid Communication
Gamou, Shinobu
Shimosato, Yukio
Merlino, Glenn T.
Shimizu, Nobuyoshi
METHYLATION STATUS OF EPIDERMAL GROWTH FACTOR RECEPTOR GENE IN LUNG CARCINOMA CELLS
title METHYLATION STATUS OF EPIDERMAL GROWTH FACTOR RECEPTOR GENE IN LUNG CARCINOMA CELLS
title_full METHYLATION STATUS OF EPIDERMAL GROWTH FACTOR RECEPTOR GENE IN LUNG CARCINOMA CELLS
title_fullStr METHYLATION STATUS OF EPIDERMAL GROWTH FACTOR RECEPTOR GENE IN LUNG CARCINOMA CELLS
title_full_unstemmed METHYLATION STATUS OF EPIDERMAL GROWTH FACTOR RECEPTOR GENE IN LUNG CARCINOMA CELLS
title_short METHYLATION STATUS OF EPIDERMAL GROWTH FACTOR RECEPTOR GENE IN LUNG CARCINOMA CELLS
title_sort methylation status of epidermal growth factor receptor gene in lung carcinoma cells
topic Rapid Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5917620/
https://www.ncbi.nlm.nih.gov/pubmed/2848004
http://dx.doi.org/10.1111/j.1349-7006.1988.tb00065.x
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