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Changes in c-onc expression during embryonal carcinoma cell differentiation.

Protooncogenes expressed in murine embryonal carcinoma (EC) cells or their differentiated daughter cells include more or less ubiquitously expressed protooncogenes such as c-myc, c-K-ras, and c-abl, as well as c-onc genes with a very restricted expression pattern. Examples of the latter are N-myc, c...

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Detalles Bibliográficos
Autores principales: Sejersen, T, Jin, P, Rahm, M, Ringertz, N R
Formato: Texto
Lenguaje:English
Publicado: 1989
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1567617/
https://www.ncbi.nlm.nih.gov/pubmed/2647482
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author Sejersen, T
Jin, P
Rahm, M
Ringertz, N R
author_facet Sejersen, T
Jin, P
Rahm, M
Ringertz, N R
author_sort Sejersen, T
collection PubMed
description Protooncogenes expressed in murine embryonal carcinoma (EC) cells or their differentiated daughter cells include more or less ubiquitously expressed protooncogenes such as c-myc, c-K-ras, and c-abl, as well as c-onc genes with a very restricted expression pattern. Examples of the latter are N-myc, c-mos, and int-2. These c-onc genes are transcriptionally active in EC cells, as well as in germ cells and/or early embryonic cells. When EC cells are induced to differentiate some protooncogenes or oncogene-related products undergo changes in expression. Thus, EC cell differentiation has been associated with increased expression of c-src, c-fos, int-1, int-2, and the epidermal growth factor (EGF) receptor, whereas decreased expression has been observed for c-mos, c-K-ras, c-myc, N-myc, and platelet-derived growth factor. The relationships between these changes in expression and EC cell differentiation are not understood. They may be important for the differentiation process or for expression of a differentiated phenotype. They may, however, also be secondary events with no functional significance to EC cell differentiation.
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spelling pubmed-15676172006-09-18 Changes in c-onc expression during embryonal carcinoma cell differentiation. Sejersen, T Jin, P Rahm, M Ringertz, N R Environ Health Perspect Research Article Protooncogenes expressed in murine embryonal carcinoma (EC) cells or their differentiated daughter cells include more or less ubiquitously expressed protooncogenes such as c-myc, c-K-ras, and c-abl, as well as c-onc genes with a very restricted expression pattern. Examples of the latter are N-myc, c-mos, and int-2. These c-onc genes are transcriptionally active in EC cells, as well as in germ cells and/or early embryonic cells. When EC cells are induced to differentiate some protooncogenes or oncogene-related products undergo changes in expression. Thus, EC cell differentiation has been associated with increased expression of c-src, c-fos, int-1, int-2, and the epidermal growth factor (EGF) receptor, whereas decreased expression has been observed for c-mos, c-K-ras, c-myc, N-myc, and platelet-derived growth factor. The relationships between these changes in expression and EC cell differentiation are not understood. They may be important for the differentiation process or for expression of a differentiated phenotype. They may, however, also be secondary events with no functional significance to EC cell differentiation. 1989-03 /pmc/articles/PMC1567617/ /pubmed/2647482 Text en
spellingShingle Research Article
Sejersen, T
Jin, P
Rahm, M
Ringertz, N R
Changes in c-onc expression during embryonal carcinoma cell differentiation.
title Changes in c-onc expression during embryonal carcinoma cell differentiation.
title_full Changes in c-onc expression during embryonal carcinoma cell differentiation.
title_fullStr Changes in c-onc expression during embryonal carcinoma cell differentiation.
title_full_unstemmed Changes in c-onc expression during embryonal carcinoma cell differentiation.
title_short Changes in c-onc expression during embryonal carcinoma cell differentiation.
title_sort changes in c-onc expression during embryonal carcinoma cell differentiation.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1567617/
https://www.ncbi.nlm.nih.gov/pubmed/2647482
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