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A distinct molecular profile associated with mucinous epithelial ovarian cancer
Mucinous epithelial ovarian cancers (MOC) are clinically and morphologically distinct from the other histological subtypes of ovarian cancer. To determine the genetic basis of MOC and to identify potential tumour markers, gene expression profiling of 49 primary ovarian cancers of different histologi...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361366/ https://www.ncbi.nlm.nih.gov/pubmed/16508639 http://dx.doi.org/10.1038/sj.bjc.6603003 |
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author | Heinzelmann-Schwarz, V A Gardiner-Garden, M Henshall, S M Scurry, J P Scolyer, R A Smith, A N Bali, A Bergh, P Vanden Baron-Hay, S Scott, C Fink, D Hacker, N F Sutherland, R L O'Brien, P M |
author_facet | Heinzelmann-Schwarz, V A Gardiner-Garden, M Henshall, S M Scurry, J P Scolyer, R A Smith, A N Bali, A Bergh, P Vanden Baron-Hay, S Scott, C Fink, D Hacker, N F Sutherland, R L O'Brien, P M |
author_sort | Heinzelmann-Schwarz, V A |
collection | PubMed |
description | Mucinous epithelial ovarian cancers (MOC) are clinically and morphologically distinct from the other histological subtypes of ovarian cancer. To determine the genetic basis of MOC and to identify potential tumour markers, gene expression profiling of 49 primary ovarian cancers of different histological subtypes was performed using a customised oligonucleotide microarray containing >59 000 probesets. The results show that MOC express a genetic profile that both differs and overlaps with other subtypes of epithelial ovarian cancer. Concordant with its histological phenotype, MOC express genes characteristic of mucinous carcinomas of varying epithelial origin, including intestinal carcinomas. Differences in gene expression between MOC and other histological subtypes of ovarian cancer were confirmed by RT–PCR and/or immunohistochemistry. In particular, galectin 4 (LGALS4) was highly and specifically expressed in MOC, but expressed at lower levels in benign mucinous cysts and borderline (atypical proliferative) tumours, supporting a malignant progression model of MOC. Hence LGALS4 may have application as an early and differential diagnostic marker of MOC. |
format | Text |
id | pubmed-2361366 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23613662009-09-10 A distinct molecular profile associated with mucinous epithelial ovarian cancer Heinzelmann-Schwarz, V A Gardiner-Garden, M Henshall, S M Scurry, J P Scolyer, R A Smith, A N Bali, A Bergh, P Vanden Baron-Hay, S Scott, C Fink, D Hacker, N F Sutherland, R L O'Brien, P M Br J Cancer Molecular Diagnostics Mucinous epithelial ovarian cancers (MOC) are clinically and morphologically distinct from the other histological subtypes of ovarian cancer. To determine the genetic basis of MOC and to identify potential tumour markers, gene expression profiling of 49 primary ovarian cancers of different histological subtypes was performed using a customised oligonucleotide microarray containing >59 000 probesets. The results show that MOC express a genetic profile that both differs and overlaps with other subtypes of epithelial ovarian cancer. Concordant with its histological phenotype, MOC express genes characteristic of mucinous carcinomas of varying epithelial origin, including intestinal carcinomas. Differences in gene expression between MOC and other histological subtypes of ovarian cancer were confirmed by RT–PCR and/or immunohistochemistry. In particular, galectin 4 (LGALS4) was highly and specifically expressed in MOC, but expressed at lower levels in benign mucinous cysts and borderline (atypical proliferative) tumours, supporting a malignant progression model of MOC. Hence LGALS4 may have application as an early and differential diagnostic marker of MOC. Nature Publishing Group 2006-03-27 2006-02-28 /pmc/articles/PMC2361366/ /pubmed/16508639 http://dx.doi.org/10.1038/sj.bjc.6603003 Text en Copyright © 2006 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 Diagnostics Heinzelmann-Schwarz, V A Gardiner-Garden, M Henshall, S M Scurry, J P Scolyer, R A Smith, A N Bali, A Bergh, P Vanden Baron-Hay, S Scott, C Fink, D Hacker, N F Sutherland, R L O'Brien, P M A distinct molecular profile associated with mucinous epithelial ovarian cancer |
title | A distinct molecular profile associated with mucinous epithelial ovarian cancer |
title_full | A distinct molecular profile associated with mucinous epithelial ovarian cancer |
title_fullStr | A distinct molecular profile associated with mucinous epithelial ovarian cancer |
title_full_unstemmed | A distinct molecular profile associated with mucinous epithelial ovarian cancer |
title_short | A distinct molecular profile associated with mucinous epithelial ovarian cancer |
title_sort | distinct molecular profile associated with mucinous epithelial ovarian cancer |
topic | Molecular Diagnostics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361366/ https://www.ncbi.nlm.nih.gov/pubmed/16508639 http://dx.doi.org/10.1038/sj.bjc.6603003 |
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