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Identification of amplified and highly expressed genes in amplicons of the T-cell line huT78 detected by cDNA microarray CGH

BACKGROUND: Conventional Comparative Genomic Hybridization (CGH) has been widely used for detecting copy number alterations in cancer and for identifying regions containing candidate tumor responsible genes. Recently, several studies have shown the utility of cDNA microarray CGH for studing gene cop...

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Autores principales: Meléndez, Bárbara, Martínez-Delgado, Beatriz, Cuadros, Marta, Fernández, Victoria, Díaz-Uriarte, Ramón, Benítez, Javier
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC546232/
https://www.ncbi.nlm.nih.gov/pubmed/15656903
http://dx.doi.org/10.1186/1476-4598-4-5
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author Meléndez, Bárbara
Martínez-Delgado, Beatriz
Cuadros, Marta
Fernández, Victoria
Díaz-Uriarte, Ramón
Benítez, Javier
author_facet Meléndez, Bárbara
Martínez-Delgado, Beatriz
Cuadros, Marta
Fernández, Victoria
Díaz-Uriarte, Ramón
Benítez, Javier
author_sort Meléndez, Bárbara
collection PubMed
description BACKGROUND: Conventional Comparative Genomic Hybridization (CGH) has been widely used for detecting copy number alterations in cancer and for identifying regions containing candidate tumor responsible genes. Recently, several studies have shown the utility of cDNA microarray CGH for studing gene copy changes in various types of tumors. However, no such studies on T-cell lymphomas have been performed. To date T-cell lymphomas analyzed by the use of chromosome CGH have revealed only slight copy number alterations and not gene amplifications. RESULTS: In the present study, we describe the characterization of three amplicons of the T-cell line huT78 located at 2q34-q37, 8q23-q24 and 20p, where new amplified and overexpressed genes are found. The use of a cDNA microarray containing 7.657 transcripts allowed the identification of certain genes, such as BCLX, PCNA, FKBP1A, IGFBP2 and cMYC, that are amplified, highly expressed, and also contained in the amplicons on 20p and 2q. The expresion of these genes was analyzed in 39 T-cell lymphomas and 3 other T-cell lines. CONCLUSION: By the use of conventional CGH and CGH and expression cDNA microarrays we defined three amplicons in the T-cell line huT78 and identified several novel gene amplifications (BCLX, PCNA, FKBP1A, IGFBP2 and cMYC). We showed that overexpression of the amplified genes could be attributable to gene dosage. We speculate that deregulation of those genes could be important in the development of T-cell lymphomas and/or in the maintenance of T-cell lines.
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spelling pubmed-5462322005-01-30 Identification of amplified and highly expressed genes in amplicons of the T-cell line huT78 detected by cDNA microarray CGH Meléndez, Bárbara Martínez-Delgado, Beatriz Cuadros, Marta Fernández, Victoria Díaz-Uriarte, Ramón Benítez, Javier Mol Cancer Short Communication BACKGROUND: Conventional Comparative Genomic Hybridization (CGH) has been widely used for detecting copy number alterations in cancer and for identifying regions containing candidate tumor responsible genes. Recently, several studies have shown the utility of cDNA microarray CGH for studing gene copy changes in various types of tumors. However, no such studies on T-cell lymphomas have been performed. To date T-cell lymphomas analyzed by the use of chromosome CGH have revealed only slight copy number alterations and not gene amplifications. RESULTS: In the present study, we describe the characterization of three amplicons of the T-cell line huT78 located at 2q34-q37, 8q23-q24 and 20p, where new amplified and overexpressed genes are found. The use of a cDNA microarray containing 7.657 transcripts allowed the identification of certain genes, such as BCLX, PCNA, FKBP1A, IGFBP2 and cMYC, that are amplified, highly expressed, and also contained in the amplicons on 20p and 2q. The expresion of these genes was analyzed in 39 T-cell lymphomas and 3 other T-cell lines. CONCLUSION: By the use of conventional CGH and CGH and expression cDNA microarrays we defined three amplicons in the T-cell line huT78 and identified several novel gene amplifications (BCLX, PCNA, FKBP1A, IGFBP2 and cMYC). We showed that overexpression of the amplified genes could be attributable to gene dosage. We speculate that deregulation of those genes could be important in the development of T-cell lymphomas and/or in the maintenance of T-cell lines. BioMed Central 2005-01-18 /pmc/articles/PMC546232/ /pubmed/15656903 http://dx.doi.org/10.1186/1476-4598-4-5 Text en Copyright © 2005 Meléndez 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 Short Communication
Meléndez, Bárbara
Martínez-Delgado, Beatriz
Cuadros, Marta
Fernández, Victoria
Díaz-Uriarte, Ramón
Benítez, Javier
Identification of amplified and highly expressed genes in amplicons of the T-cell line huT78 detected by cDNA microarray CGH
title Identification of amplified and highly expressed genes in amplicons of the T-cell line huT78 detected by cDNA microarray CGH
title_full Identification of amplified and highly expressed genes in amplicons of the T-cell line huT78 detected by cDNA microarray CGH
title_fullStr Identification of amplified and highly expressed genes in amplicons of the T-cell line huT78 detected by cDNA microarray CGH
title_full_unstemmed Identification of amplified and highly expressed genes in amplicons of the T-cell line huT78 detected by cDNA microarray CGH
title_short Identification of amplified and highly expressed genes in amplicons of the T-cell line huT78 detected by cDNA microarray CGH
title_sort identification of amplified and highly expressed genes in amplicons of the t-cell line hut78 detected by cdna microarray cgh
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC546232/
https://www.ncbi.nlm.nih.gov/pubmed/15656903
http://dx.doi.org/10.1186/1476-4598-4-5
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