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Gene expression profiling identifies tumour markers potentially playing a role in uveal melanoma development
Microarray is a powerful tool to compare the gene expression of different tumour specimens and cell lines simultaneously and quantitatively. To get a better insight into genes that are involved in uveal melanoma tumorigenesis, we compared the gene expression profiles of 12 different uveal melanoma c...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2003
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2394439/ https://www.ncbi.nlm.nih.gov/pubmed/14612903 http://dx.doi.org/10.1038/sj.bjc.6601374 |
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author | Zuidervaart, W van der Velden, P A Hurks, M H van Nieuwpoort, F A Out-Luiting, C J J Singh, A D Frants, R R Jager, M J Gruis, N A |
author_facet | Zuidervaart, W van der Velden, P A Hurks, M H van Nieuwpoort, F A Out-Luiting, C J J Singh, A D Frants, R R Jager, M J Gruis, N A |
author_sort | Zuidervaart, W |
collection | PubMed |
description | Microarray is a powerful tool to compare the gene expression of different tumour specimens and cell lines simultaneously and quantitatively. To get a better insight into genes that are involved in uveal melanoma tumorigenesis, we compared the gene expression profiles of 12 different uveal melanoma cell lines with three melanocyte cell cultures obtained from healthy donor eyes. Gene expression profiles were obtained by nylon filter arrays, containing 1176 gene spots related to cancer development. The expression levels of selected genes were validated on cell lines and primary uveal melanomas by real time RT–PCR, and were subsequently included in cluster analysis. Four candidate tumour markers, Laminin Receptor 1, Endothelin 2, Von Hippel Lindau Binding protein 1 and Cullin 2, have been selected from genes that were differentially expressed in the uveal melanoma cell lines compared to the normal uveal melanocytes. In primary uveal melanomas, these four markers could discriminate between two classes of uveal melanoma, which may be indicative of a differential disease process. |
format | Text |
id | pubmed-2394439 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2003 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23944392009-09-10 Gene expression profiling identifies tumour markers potentially playing a role in uveal melanoma development Zuidervaart, W van der Velden, P A Hurks, M H van Nieuwpoort, F A Out-Luiting, C J J Singh, A D Frants, R R Jager, M J Gruis, N A Br J Cancer Molecular and Cellular Pathology Microarray is a powerful tool to compare the gene expression of different tumour specimens and cell lines simultaneously and quantitatively. To get a better insight into genes that are involved in uveal melanoma tumorigenesis, we compared the gene expression profiles of 12 different uveal melanoma cell lines with three melanocyte cell cultures obtained from healthy donor eyes. Gene expression profiles were obtained by nylon filter arrays, containing 1176 gene spots related to cancer development. The expression levels of selected genes were validated on cell lines and primary uveal melanomas by real time RT–PCR, and were subsequently included in cluster analysis. Four candidate tumour markers, Laminin Receptor 1, Endothelin 2, Von Hippel Lindau Binding protein 1 and Cullin 2, have been selected from genes that were differentially expressed in the uveal melanoma cell lines compared to the normal uveal melanocytes. In primary uveal melanomas, these four markers could discriminate between two classes of uveal melanoma, which may be indicative of a differential disease process. Nature Publishing Group 2003-11-17 2003-11-11 /pmc/articles/PMC2394439/ /pubmed/14612903 http://dx.doi.org/10.1038/sj.bjc.6601374 Text en Copyright © 2003 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Molecular and Cellular Pathology Zuidervaart, W van der Velden, P A Hurks, M H van Nieuwpoort, F A Out-Luiting, C J J Singh, A D Frants, R R Jager, M J Gruis, N A Gene expression profiling identifies tumour markers potentially playing a role in uveal melanoma development |
title | Gene expression profiling identifies tumour markers potentially playing a role in uveal melanoma development |
title_full | Gene expression profiling identifies tumour markers potentially playing a role in uveal melanoma development |
title_fullStr | Gene expression profiling identifies tumour markers potentially playing a role in uveal melanoma development |
title_full_unstemmed | Gene expression profiling identifies tumour markers potentially playing a role in uveal melanoma development |
title_short | Gene expression profiling identifies tumour markers potentially playing a role in uveal melanoma development |
title_sort | gene expression profiling identifies tumour markers potentially playing a role in uveal melanoma development |
topic | Molecular and Cellular Pathology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2394439/ https://www.ncbi.nlm.nih.gov/pubmed/14612903 http://dx.doi.org/10.1038/sj.bjc.6601374 |
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