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Mapping of the chromosomal amplification 1p21-22 in bladder cancer

BACKGROUND: The aim of the study was to characterize a recurrent amplification at chromosomal region 1p21-22 in bladder cancer. METHODS: ArrayCGH (aCGH) was performed to identify DNA copy number variations in 7 clinical samples and 6 bladder cancer cell lines. FISH was used to map the amplicon at 1p...

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Autores principales: Scaravilli, Mauro, Asero, Paola, Tammela, Teuvo LJ, Visakorpi, Tapio, Saramäki, Outi R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4143550/
https://www.ncbi.nlm.nih.gov/pubmed/25135188
http://dx.doi.org/10.1186/1756-0500-7-547
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author Scaravilli, Mauro
Asero, Paola
Tammela, Teuvo LJ
Visakorpi, Tapio
Saramäki, Outi R
author_facet Scaravilli, Mauro
Asero, Paola
Tammela, Teuvo LJ
Visakorpi, Tapio
Saramäki, Outi R
author_sort Scaravilli, Mauro
collection PubMed
description BACKGROUND: The aim of the study was to characterize a recurrent amplification at chromosomal region 1p21-22 in bladder cancer. METHODS: ArrayCGH (aCGH) was performed to identify DNA copy number variations in 7 clinical samples and 6 bladder cancer cell lines. FISH was used to map the amplicon at 1p21-22 in the cell lines. Gene expression microarrays and qRT-PCR were used to study the expression of putative target genes in the region. RESULTS: aCGH identified an amplification at 1p21-22 in 10/13 (77%) samples. The minimal region of the amplification was mapped to a region of about 1 Mb in size, containing a total of 11 known genes. The highest amplification was found in SCaBER squamous cell carcinoma cell line. Four genes, TMED5, DR1, RPL5 and EVI5, showed significant overexpression in the SCaBER cell line compared to all the other samples tested. Oncomine database analysis revealed upregulation of DR1 in superficial and infiltrating bladder cancer samples, compared to normal bladder. CONCLUSIONS: In conclusions, we have identified and mapped chromosomal amplification at 1p21-22 in bladder cancer as well as studied the expression of the genes in the region. DR1 was found to be significantly overexpressed in the SCaBER, which is a model of squamous cell carcinoma. However, the overexpression was found also in a published clinical sample cohort of superficial and infiltrating bladder cancers. Further studies with more clinical material are needed to investigate the role of the amplification at 1p21-22.
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spelling pubmed-41435502014-08-27 Mapping of the chromosomal amplification 1p21-22 in bladder cancer Scaravilli, Mauro Asero, Paola Tammela, Teuvo LJ Visakorpi, Tapio Saramäki, Outi R BMC Res Notes Research Article BACKGROUND: The aim of the study was to characterize a recurrent amplification at chromosomal region 1p21-22 in bladder cancer. METHODS: ArrayCGH (aCGH) was performed to identify DNA copy number variations in 7 clinical samples and 6 bladder cancer cell lines. FISH was used to map the amplicon at 1p21-22 in the cell lines. Gene expression microarrays and qRT-PCR were used to study the expression of putative target genes in the region. RESULTS: aCGH identified an amplification at 1p21-22 in 10/13 (77%) samples. The minimal region of the amplification was mapped to a region of about 1 Mb in size, containing a total of 11 known genes. The highest amplification was found in SCaBER squamous cell carcinoma cell line. Four genes, TMED5, DR1, RPL5 and EVI5, showed significant overexpression in the SCaBER cell line compared to all the other samples tested. Oncomine database analysis revealed upregulation of DR1 in superficial and infiltrating bladder cancer samples, compared to normal bladder. CONCLUSIONS: In conclusions, we have identified and mapped chromosomal amplification at 1p21-22 in bladder cancer as well as studied the expression of the genes in the region. DR1 was found to be significantly overexpressed in the SCaBER, which is a model of squamous cell carcinoma. However, the overexpression was found also in a published clinical sample cohort of superficial and infiltrating bladder cancers. Further studies with more clinical material are needed to investigate the role of the amplification at 1p21-22. BioMed Central 2014-08-18 /pmc/articles/PMC4143550/ /pubmed/25135188 http://dx.doi.org/10.1186/1756-0500-7-547 Text en © Scaravilli et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Scaravilli, Mauro
Asero, Paola
Tammela, Teuvo LJ
Visakorpi, Tapio
Saramäki, Outi R
Mapping of the chromosomal amplification 1p21-22 in bladder cancer
title Mapping of the chromosomal amplification 1p21-22 in bladder cancer
title_full Mapping of the chromosomal amplification 1p21-22 in bladder cancer
title_fullStr Mapping of the chromosomal amplification 1p21-22 in bladder cancer
title_full_unstemmed Mapping of the chromosomal amplification 1p21-22 in bladder cancer
title_short Mapping of the chromosomal amplification 1p21-22 in bladder cancer
title_sort mapping of the chromosomal amplification 1p21-22 in bladder cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4143550/
https://www.ncbi.nlm.nih.gov/pubmed/25135188
http://dx.doi.org/10.1186/1756-0500-7-547
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