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Expression of the extracellular matrix protein tenascin in malignant and benign ovarian tumours.
The extracellular matrix protein tenascin (TN) is overexpressed in a number of solid tumours. Thi however, is the first study to examine TN expression in ovarian tumours. TN protein was examined in froze sections of 50 human ovarian tumours by immunohistochemistry. Malignant and borderline tumours s...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
1996
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2077103/ https://www.ncbi.nlm.nih.gov/pubmed/8855965 |
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author | Wilson, K. E. Langdon, S. P. Lessells, A. M. Miller, W. R. |
author_facet | Wilson, K. E. Langdon, S. P. Lessells, A. M. Miller, W. R. |
author_sort | Wilson, K. E. |
collection | PubMed |
description | The extracellular matrix protein tenascin (TN) is overexpressed in a number of solid tumours. Thi however, is the first study to examine TN expression in ovarian tumours. TN protein was examined in froze sections of 50 human ovarian tumours by immunohistochemistry. Malignant and borderline tumours showed significantly greater incidence and intensity of stromal staining than benign tumours (P < 0.0001 and P = 0.038 respectively). Seven omental metastases were also examined and showed a strikingly similar protein distribution to their primary tumour counterparts. The expression pattern of different RNA isoforms, created by alternative splicing of the primary transcript, was identified using reverse transcription-polymerase chain reactions (RT-PCR). The smallest TN RNA splice variant (284 bp) was found in all tumours examined, while the appearance of larger molecular weight transcripts (approximately 490 and 556 bp), as major forms, was predominantly limited to malignant tumours, with 9/12 malignant tumours showing this pattern compared with 1/6 benign tumours. These data suggest that malignant ovarian tumours have increased expression of TN compared with benign tumours and this may be associated with induction of specific isoforms. IMAGES: |
format | Text |
id | pubmed-2077103 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1996 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-20771032009-09-10 Expression of the extracellular matrix protein tenascin in malignant and benign ovarian tumours. Wilson, K. E. Langdon, S. P. Lessells, A. M. Miller, W. R. Br J Cancer Research Article The extracellular matrix protein tenascin (TN) is overexpressed in a number of solid tumours. Thi however, is the first study to examine TN expression in ovarian tumours. TN protein was examined in froze sections of 50 human ovarian tumours by immunohistochemistry. Malignant and borderline tumours showed significantly greater incidence and intensity of stromal staining than benign tumours (P < 0.0001 and P = 0.038 respectively). Seven omental metastases were also examined and showed a strikingly similar protein distribution to their primary tumour counterparts. The expression pattern of different RNA isoforms, created by alternative splicing of the primary transcript, was identified using reverse transcription-polymerase chain reactions (RT-PCR). The smallest TN RNA splice variant (284 bp) was found in all tumours examined, while the appearance of larger molecular weight transcripts (approximately 490 and 556 bp), as major forms, was predominantly limited to malignant tumours, with 9/12 malignant tumours showing this pattern compared with 1/6 benign tumours. These data suggest that malignant ovarian tumours have increased expression of TN compared with benign tumours and this may be associated with induction of specific isoforms. IMAGES: Nature Publishing Group 1996-10 /pmc/articles/PMC2077103/ /pubmed/8855965 Text en 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 | Research Article Wilson, K. E. Langdon, S. P. Lessells, A. M. Miller, W. R. Expression of the extracellular matrix protein tenascin in malignant and benign ovarian tumours. |
title | Expression of the extracellular matrix protein tenascin in malignant and benign ovarian tumours. |
title_full | Expression of the extracellular matrix protein tenascin in malignant and benign ovarian tumours. |
title_fullStr | Expression of the extracellular matrix protein tenascin in malignant and benign ovarian tumours. |
title_full_unstemmed | Expression of the extracellular matrix protein tenascin in malignant and benign ovarian tumours. |
title_short | Expression of the extracellular matrix protein tenascin in malignant and benign ovarian tumours. |
title_sort | expression of the extracellular matrix protein tenascin in malignant and benign ovarian tumours. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2077103/ https://www.ncbi.nlm.nih.gov/pubmed/8855965 |
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