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Colorectal adenoma to carcinoma progression is accompanied by changes in gene expression associated with ageing, chromosomal instability, and fatty acid metabolism

BACKGROUND: Colorectal cancer develops in a multi-step manner from normal epithelium, through a pre-malignant lesion (so-called adenoma), into a malignant lesion (carcinoma), which invades surrounding tissues and eventually can spread systemically (metastasis). It is estimated that only about 5% of...

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Autores principales: Carvalho, Beatriz, Sillars-Hardebol, Anke H., Postma, Cindy, Mongera, Sandra, Droste, Jochim Terhaar Sive, Obulkasim, Askar, van de Wiel, Mark, van Criekinge, Wim, Ylstra, Bauke, Fijneman, Remond J. A., Meijer, Gerrit A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3308003/
https://www.ncbi.nlm.nih.gov/pubmed/22278361
http://dx.doi.org/10.1007/s13402-011-0065-1
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author Carvalho, Beatriz
Sillars-Hardebol, Anke H.
Postma, Cindy
Mongera, Sandra
Droste, Jochim Terhaar Sive
Obulkasim, Askar
van de Wiel, Mark
van Criekinge, Wim
Ylstra, Bauke
Fijneman, Remond J. A.
Meijer, Gerrit A.
author_facet Carvalho, Beatriz
Sillars-Hardebol, Anke H.
Postma, Cindy
Mongera, Sandra
Droste, Jochim Terhaar Sive
Obulkasim, Askar
van de Wiel, Mark
van Criekinge, Wim
Ylstra, Bauke
Fijneman, Remond J. A.
Meijer, Gerrit A.
author_sort Carvalho, Beatriz
collection PubMed
description BACKGROUND: Colorectal cancer develops in a multi-step manner from normal epithelium, through a pre-malignant lesion (so-called adenoma), into a malignant lesion (carcinoma), which invades surrounding tissues and eventually can spread systemically (metastasis). It is estimated that only about 5% of adenomas do progress to a carcinoma. AIM: The present study aimed to unravel the biology of adenoma to carcinoma progression by mRNA expression profiling, and to identify candidate biomarkers for adenomas that are truly at high risk of progression. METHODS: Genome-wide mRNA expression profiles were obtained from a series of 37 colorectal adenomas and 31 colorectal carcinomas using oligonucleotide microarrays. Differentially expressed genes were validated in an independent colorectal gene expression data set. Gene Set Enrichment Analysis (GSEA) was used to identify altered expression of sets of genes associated with specific biological processes, in order to better understand the biology of colorectal adenoma to carcinoma progression. RESULTS: mRNA expression of 248 genes was significantly different, of which 96 were upregulated and 152 downregulated in carcinomas compared to adenomas. Classification of adenomas and carcinomas using the expression of these genes showed to be very accurate, also when tested in an independent expression data set. Gene-sets associated with ageing (which is related to senescence) and chromosomal instability were upregulated, and a gene-set associated with fatty acid metabolism was downregulated in carcinomas compared to adenomas. Moreover, gene-sets associated with chromosomal location revealed chromosome 4q22 loss and chromosome 20q gain of gene-set expression as being relevant in this progression. CONCLUDING REMARK: These data are consistent with the notion that adenomas and carcinomas are distinct biological entities. Disruption of specific biological processes like senescence (ageing), maintenance of chromosomal instability and altered metabolism, are key factors in the progression from adenoma to carcinoma. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s13402-011-0065-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-33080032012-03-22 Colorectal adenoma to carcinoma progression is accompanied by changes in gene expression associated with ageing, chromosomal instability, and fatty acid metabolism Carvalho, Beatriz Sillars-Hardebol, Anke H. Postma, Cindy Mongera, Sandra Droste, Jochim Terhaar Sive Obulkasim, Askar van de Wiel, Mark van Criekinge, Wim Ylstra, Bauke Fijneman, Remond J. A. Meijer, Gerrit A. Cell Oncol (Dordr) Original Paper BACKGROUND: Colorectal cancer develops in a multi-step manner from normal epithelium, through a pre-malignant lesion (so-called adenoma), into a malignant lesion (carcinoma), which invades surrounding tissues and eventually can spread systemically (metastasis). It is estimated that only about 5% of adenomas do progress to a carcinoma. AIM: The present study aimed to unravel the biology of adenoma to carcinoma progression by mRNA expression profiling, and to identify candidate biomarkers for adenomas that are truly at high risk of progression. METHODS: Genome-wide mRNA expression profiles were obtained from a series of 37 colorectal adenomas and 31 colorectal carcinomas using oligonucleotide microarrays. Differentially expressed genes were validated in an independent colorectal gene expression data set. Gene Set Enrichment Analysis (GSEA) was used to identify altered expression of sets of genes associated with specific biological processes, in order to better understand the biology of colorectal adenoma to carcinoma progression. RESULTS: mRNA expression of 248 genes was significantly different, of which 96 were upregulated and 152 downregulated in carcinomas compared to adenomas. Classification of adenomas and carcinomas using the expression of these genes showed to be very accurate, also when tested in an independent expression data set. Gene-sets associated with ageing (which is related to senescence) and chromosomal instability were upregulated, and a gene-set associated with fatty acid metabolism was downregulated in carcinomas compared to adenomas. Moreover, gene-sets associated with chromosomal location revealed chromosome 4q22 loss and chromosome 20q gain of gene-set expression as being relevant in this progression. CONCLUDING REMARK: These data are consistent with the notion that adenomas and carcinomas are distinct biological entities. Disruption of specific biological processes like senescence (ageing), maintenance of chromosomal instability and altered metabolism, are key factors in the progression from adenoma to carcinoma. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s13402-011-0065-1) contains supplementary material, which is available to authorized users. Springer Netherlands 2012-01-26 2012-02 /pmc/articles/PMC3308003/ /pubmed/22278361 http://dx.doi.org/10.1007/s13402-011-0065-1 Text en © International Society for Cellular Oncology 2012
spellingShingle Original Paper
Carvalho, Beatriz
Sillars-Hardebol, Anke H.
Postma, Cindy
Mongera, Sandra
Droste, Jochim Terhaar Sive
Obulkasim, Askar
van de Wiel, Mark
van Criekinge, Wim
Ylstra, Bauke
Fijneman, Remond J. A.
Meijer, Gerrit A.
Colorectal adenoma to carcinoma progression is accompanied by changes in gene expression associated with ageing, chromosomal instability, and fatty acid metabolism
title Colorectal adenoma to carcinoma progression is accompanied by changes in gene expression associated with ageing, chromosomal instability, and fatty acid metabolism
title_full Colorectal adenoma to carcinoma progression is accompanied by changes in gene expression associated with ageing, chromosomal instability, and fatty acid metabolism
title_fullStr Colorectal adenoma to carcinoma progression is accompanied by changes in gene expression associated with ageing, chromosomal instability, and fatty acid metabolism
title_full_unstemmed Colorectal adenoma to carcinoma progression is accompanied by changes in gene expression associated with ageing, chromosomal instability, and fatty acid metabolism
title_short Colorectal adenoma to carcinoma progression is accompanied by changes in gene expression associated with ageing, chromosomal instability, and fatty acid metabolism
title_sort colorectal adenoma to carcinoma progression is accompanied by changes in gene expression associated with ageing, chromosomal instability, and fatty acid metabolism
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3308003/
https://www.ncbi.nlm.nih.gov/pubmed/22278361
http://dx.doi.org/10.1007/s13402-011-0065-1
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