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Identification of novel neuroendocrine-specific tumour genes
Neuroendocrine tumours (NETs) comprise a heterogenous group of malignancies with an often unpredictable course, and with limited treatment options. Thus, new diagnostic, prognostic, and therapeutic markers are needed. To shed new lights into the biology of NETs, we have by cDNA transcript profiling,...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2570516/ https://www.ncbi.nlm.nih.gov/pubmed/18827820 http://dx.doi.org/10.1038/sj.bjc.6604565 |
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author | Hofsli, E Wheeler, T E Langaas, M Lægreid, A Thommesen, L |
author_facet | Hofsli, E Wheeler, T E Langaas, M Lægreid, A Thommesen, L |
author_sort | Hofsli, E |
collection | PubMed |
description | Neuroendocrine tumours (NETs) comprise a heterogenous group of malignancies with an often unpredictable course, and with limited treatment options. Thus, new diagnostic, prognostic, and therapeutic markers are needed. To shed new lights into the biology of NETs, we have by cDNA transcript profiling, sought to identify genes that are either up- or downregulated in NE as compared with non-NE tumour cells. A panel of six NET and four non-NET cell lines were examined, and out of 12 743 genes examined, we studied in detail the 200 most significantly differentially expressed genes in the comparison. In addition to potential new diagnostic markers (NEFM, CLDN4, PEROX2), the results point to genes that may be involved in the tumorigenesis (BEX1, TMEPAI, FOSL1, RAB32), and in the processes of invasion, progression and metastasis (MME, STAT3, DCBLD2) of NETs. Verification by real time qRT–PCR showed a high degree of consistency to the microarray results. Furthermore, the protein expression of some of the genes were examined. The results of our study has opened a window to new areas of research, by uncovering new candidate genes and proteins to be further investigated in the search for new prognostic, predictive, and therapeutic markers in NETs. |
format | Text |
id | pubmed-2570516 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-25705162009-10-21 Identification of novel neuroendocrine-specific tumour genes Hofsli, E Wheeler, T E Langaas, M Lægreid, A Thommesen, L Br J Cancer Genetics and Genomics Neuroendocrine tumours (NETs) comprise a heterogenous group of malignancies with an often unpredictable course, and with limited treatment options. Thus, new diagnostic, prognostic, and therapeutic markers are needed. To shed new lights into the biology of NETs, we have by cDNA transcript profiling, sought to identify genes that are either up- or downregulated in NE as compared with non-NE tumour cells. A panel of six NET and four non-NET cell lines were examined, and out of 12 743 genes examined, we studied in detail the 200 most significantly differentially expressed genes in the comparison. In addition to potential new diagnostic markers (NEFM, CLDN4, PEROX2), the results point to genes that may be involved in the tumorigenesis (BEX1, TMEPAI, FOSL1, RAB32), and in the processes of invasion, progression and metastasis (MME, STAT3, DCBLD2) of NETs. Verification by real time qRT–PCR showed a high degree of consistency to the microarray results. Furthermore, the protein expression of some of the genes were examined. The results of our study has opened a window to new areas of research, by uncovering new candidate genes and proteins to be further investigated in the search for new prognostic, predictive, and therapeutic markers in NETs. Nature Publishing Group 2008-10-21 2008-09-30 /pmc/articles/PMC2570516/ /pubmed/18827820 http://dx.doi.org/10.1038/sj.bjc.6604565 Text en Copyright © 2008 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 | Genetics and Genomics Hofsli, E Wheeler, T E Langaas, M Lægreid, A Thommesen, L Identification of novel neuroendocrine-specific tumour genes |
title | Identification of novel neuroendocrine-specific tumour genes |
title_full | Identification of novel neuroendocrine-specific tumour genes |
title_fullStr | Identification of novel neuroendocrine-specific tumour genes |
title_full_unstemmed | Identification of novel neuroendocrine-specific tumour genes |
title_short | Identification of novel neuroendocrine-specific tumour genes |
title_sort | identification of novel neuroendocrine-specific tumour genes |
topic | Genetics and Genomics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2570516/ https://www.ncbi.nlm.nih.gov/pubmed/18827820 http://dx.doi.org/10.1038/sj.bjc.6604565 |
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