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Gene expression profiling of tumours derived from ras(V12)/E1A-transformed mouse embryonic fibroblasts to identify genes required for tumour development
BACKGROUND: In cancer, cellular transformation is followed by tumour development. Knowledge on the mechanisms of transformation, involving activation of proto-oncogenes and inactivation of tumour-suppressor genes has considerably improved whereas tumour development remains poorly understood. An inte...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC546195/ https://www.ncbi.nlm.nih.gov/pubmed/15651998 http://dx.doi.org/10.1186/1476-4598-4-4 |
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author | Vasseur, Sophie Malicet, Cédric Calvo, Ezequiel L Dagorn, Jean Charles Iovanna, Juan L |
author_facet | Vasseur, Sophie Malicet, Cédric Calvo, Ezequiel L Dagorn, Jean Charles Iovanna, Juan L |
author_sort | Vasseur, Sophie |
collection | PubMed |
description | BACKGROUND: In cancer, cellular transformation is followed by tumour development. Knowledge on the mechanisms of transformation, involving activation of proto-oncogenes and inactivation of tumour-suppressor genes has considerably improved whereas tumour development remains poorly understood. An interesting way of gaining information on tumour progression mechanisms would be to identify genes whose expression is altered during tumour formation. We used the Affymetrix-based DNA microarray technology to analyze gene expression profiles of tumours derived from ras(V12)/E1A-transformed mouse embryo fibroblasts in order to identify the genes that could be involved in tumour development. RESULTS: Among the 12,000 genes analyzed in this study, only 489 showed altered expression during tumour development, 213 being up-regulated and 276 down-regulated. The genes differentially expressed are involved in a variety of cellular functions, including control of transcription, regulation of mRNA maturation and processing, regulation of protein translation, activation of interferon-induced genes, intracellular signalling, apoptosis, cell growth, angiogenesis, cytoskeleton, cell-to-cell interaction, extracellular matrix formation, metabolism and production of secretory factors. CONCLUSIONS: Some of the genes identified in this work, whose expression is altered upon ras(V12)/E1A transformation of MEFs, could be new cancer therapeutic targets. |
format | Text |
id | pubmed-546195 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-5461952005-01-30 Gene expression profiling of tumours derived from ras(V12)/E1A-transformed mouse embryonic fibroblasts to identify genes required for tumour development Vasseur, Sophie Malicet, Cédric Calvo, Ezequiel L Dagorn, Jean Charles Iovanna, Juan L Mol Cancer Research BACKGROUND: In cancer, cellular transformation is followed by tumour development. Knowledge on the mechanisms of transformation, involving activation of proto-oncogenes and inactivation of tumour-suppressor genes has considerably improved whereas tumour development remains poorly understood. An interesting way of gaining information on tumour progression mechanisms would be to identify genes whose expression is altered during tumour formation. We used the Affymetrix-based DNA microarray technology to analyze gene expression profiles of tumours derived from ras(V12)/E1A-transformed mouse embryo fibroblasts in order to identify the genes that could be involved in tumour development. RESULTS: Among the 12,000 genes analyzed in this study, only 489 showed altered expression during tumour development, 213 being up-regulated and 276 down-regulated. The genes differentially expressed are involved in a variety of cellular functions, including control of transcription, regulation of mRNA maturation and processing, regulation of protein translation, activation of interferon-induced genes, intracellular signalling, apoptosis, cell growth, angiogenesis, cytoskeleton, cell-to-cell interaction, extracellular matrix formation, metabolism and production of secretory factors. CONCLUSIONS: Some of the genes identified in this work, whose expression is altered upon ras(V12)/E1A transformation of MEFs, could be new cancer therapeutic targets. BioMed Central 2005-01-16 /pmc/articles/PMC546195/ /pubmed/15651998 http://dx.doi.org/10.1186/1476-4598-4-4 Text en Copyright © 2005 Vasseur et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Vasseur, Sophie Malicet, Cédric Calvo, Ezequiel L Dagorn, Jean Charles Iovanna, Juan L Gene expression profiling of tumours derived from ras(V12)/E1A-transformed mouse embryonic fibroblasts to identify genes required for tumour development |
title | Gene expression profiling of tumours derived from ras(V12)/E1A-transformed mouse embryonic fibroblasts to identify genes required for tumour development |
title_full | Gene expression profiling of tumours derived from ras(V12)/E1A-transformed mouse embryonic fibroblasts to identify genes required for tumour development |
title_fullStr | Gene expression profiling of tumours derived from ras(V12)/E1A-transformed mouse embryonic fibroblasts to identify genes required for tumour development |
title_full_unstemmed | Gene expression profiling of tumours derived from ras(V12)/E1A-transformed mouse embryonic fibroblasts to identify genes required for tumour development |
title_short | Gene expression profiling of tumours derived from ras(V12)/E1A-transformed mouse embryonic fibroblasts to identify genes required for tumour development |
title_sort | gene expression profiling of tumours derived from ras(v12)/e1a-transformed mouse embryonic fibroblasts to identify genes required for tumour development |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC546195/ https://www.ncbi.nlm.nih.gov/pubmed/15651998 http://dx.doi.org/10.1186/1476-4598-4-4 |
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