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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...

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Autores principales: Vasseur, Sophie, Malicet, Cédric, Calvo, Ezequiel L, Dagorn, Jean Charles, Iovanna, Juan L
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
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.
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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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