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A genome-wide map of aberrantly expressed chromosomal islands in colorectal cancer

BACKGROUND: Cancer development is accompanied by genetic phenomena like deletion and amplification of chromosome parts or alterations of chromatin structure. It is expected that these mechanisms have a strong effect on regional gene expression. RESULTS: We investigated genome-wide gene expression in...

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Autores principales: Staub, Eike, Gröne, Jörn, Mennerich, Detlev, Röpcke, Stefan, Klamann, Irina, Hinzmann, Bernd, Castanos-Velez, Esmeralda, Mann, Benno, Pilarsky, Christian, Brümmendorf, Thomas, Weber, Birgit, Buhr, Heinz-Johannes, Rosenthal, André
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1601966/
https://www.ncbi.nlm.nih.gov/pubmed/16982006
http://dx.doi.org/10.1186/1476-4598-5-37
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author Staub, Eike
Gröne, Jörn
Mennerich, Detlev
Röpcke, Stefan
Klamann, Irina
Hinzmann, Bernd
Castanos-Velez, Esmeralda
Mann, Benno
Pilarsky, Christian
Brümmendorf, Thomas
Weber, Birgit
Buhr, Heinz-Johannes
Rosenthal, André
author_facet Staub, Eike
Gröne, Jörn
Mennerich, Detlev
Röpcke, Stefan
Klamann, Irina
Hinzmann, Bernd
Castanos-Velez, Esmeralda
Mann, Benno
Pilarsky, Christian
Brümmendorf, Thomas
Weber, Birgit
Buhr, Heinz-Johannes
Rosenthal, André
author_sort Staub, Eike
collection PubMed
description BACKGROUND: Cancer development is accompanied by genetic phenomena like deletion and amplification of chromosome parts or alterations of chromatin structure. It is expected that these mechanisms have a strong effect on regional gene expression. RESULTS: We investigated genome-wide gene expression in colorectal carcinoma (CRC) and normal epithelial tissues from 25 patients using oligonucleotide arrays. This allowed us to identify 81 distinct chromosomal islands with aberrant gene expression. Of these, 38 islands show a gain in expression and 43 a loss of expression. In total, 7.892 genes (25.3% of all human genes) are located in aberrantly expressed islands. Many chromosomal regions that are linked to hereditary colorectal cancer show deregulated expression. Also, many known tumor genes localize to chromosomal islands of misregulated expression in CRC. CONCLUSION: An extensive comparison with published CGH data suggests that chromosomal regions known for frequent deletions in colon cancer tend to show reduced expression. In contrast, regions that are often amplified in colorectal tumors exhibit heterogeneous expression patterns: even show a decrease of mRNA expression. Because for several islands of deregulated expression chromosomal aberrations have never been observed, we speculate that additional mechanisms (like abnormal states of regional chromatin) also have a substantial impact on the formation of co-expression islands in colorectal carcinoma.
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spelling pubmed-16019662006-10-13 A genome-wide map of aberrantly expressed chromosomal islands in colorectal cancer Staub, Eike Gröne, Jörn Mennerich, Detlev Röpcke, Stefan Klamann, Irina Hinzmann, Bernd Castanos-Velez, Esmeralda Mann, Benno Pilarsky, Christian Brümmendorf, Thomas Weber, Birgit Buhr, Heinz-Johannes Rosenthal, André Mol Cancer Research BACKGROUND: Cancer development is accompanied by genetic phenomena like deletion and amplification of chromosome parts or alterations of chromatin structure. It is expected that these mechanisms have a strong effect on regional gene expression. RESULTS: We investigated genome-wide gene expression in colorectal carcinoma (CRC) and normal epithelial tissues from 25 patients using oligonucleotide arrays. This allowed us to identify 81 distinct chromosomal islands with aberrant gene expression. Of these, 38 islands show a gain in expression and 43 a loss of expression. In total, 7.892 genes (25.3% of all human genes) are located in aberrantly expressed islands. Many chromosomal regions that are linked to hereditary colorectal cancer show deregulated expression. Also, many known tumor genes localize to chromosomal islands of misregulated expression in CRC. CONCLUSION: An extensive comparison with published CGH data suggests that chromosomal regions known for frequent deletions in colon cancer tend to show reduced expression. In contrast, regions that are often amplified in colorectal tumors exhibit heterogeneous expression patterns: even show a decrease of mRNA expression. Because for several islands of deregulated expression chromosomal aberrations have never been observed, we speculate that additional mechanisms (like abnormal states of regional chromatin) also have a substantial impact on the formation of co-expression islands in colorectal carcinoma. BioMed Central 2006-09-18 /pmc/articles/PMC1601966/ /pubmed/16982006 http://dx.doi.org/10.1186/1476-4598-5-37 Text en Copyright © 2006 Staub 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
Staub, Eike
Gröne, Jörn
Mennerich, Detlev
Röpcke, Stefan
Klamann, Irina
Hinzmann, Bernd
Castanos-Velez, Esmeralda
Mann, Benno
Pilarsky, Christian
Brümmendorf, Thomas
Weber, Birgit
Buhr, Heinz-Johannes
Rosenthal, André
A genome-wide map of aberrantly expressed chromosomal islands in colorectal cancer
title A genome-wide map of aberrantly expressed chromosomal islands in colorectal cancer
title_full A genome-wide map of aberrantly expressed chromosomal islands in colorectal cancer
title_fullStr A genome-wide map of aberrantly expressed chromosomal islands in colorectal cancer
title_full_unstemmed A genome-wide map of aberrantly expressed chromosomal islands in colorectal cancer
title_short A genome-wide map of aberrantly expressed chromosomal islands in colorectal cancer
title_sort genome-wide map of aberrantly expressed chromosomal islands in colorectal cancer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1601966/
https://www.ncbi.nlm.nih.gov/pubmed/16982006
http://dx.doi.org/10.1186/1476-4598-5-37
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