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Expressions of Fas ligand and other apoptosis-related genes and their prognostic significance in epithelial ovarian neoplasms
SummaryExpression of apoptosis-related proteins, bcl-2, Bax, Fas and Fas ligand (L), in ovarian epithelial neoplasms together with its clinical relevance was examined by immunohistochemistry. They included 36 cases with adenoma, 33 with low potential malignancy (LPM) and 63 with carcinomas. bcl-2 ex...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2000
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363379/ https://www.ncbi.nlm.nih.gov/pubmed/10780525 http://dx.doi.org/10.1054/bjoc.1999.1073 |
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author | Munakata*, S Enomoto, T Tsujimoto, M Otsuki, Y Miwa, H Kanno, H Aozasa, K |
author_facet | Munakata*, S Enomoto, T Tsujimoto, M Otsuki, Y Miwa, H Kanno, H Aozasa, K |
author_sort | Munakata*, S |
collection | PubMed |
description | SummaryExpression of apoptosis-related proteins, bcl-2, Bax, Fas and Fas ligand (L), in ovarian epithelial neoplasms together with its clinical relevance was examined by immunohistochemistry. They included 36 cases with adenoma, 33 with low potential malignancy (LPM) and 63 with carcinomas. bcl-2 expression was observed in 14 of 36 cases (39%) with adenoma, five of 33 (15%) with LPM (P< 0.05) and 12 of 63 (19%) with carcinoma (P< 0.05). Cases with bcl-2 expression showed more favourable prognosis than those without, but the difference was not statistically significant. There was no difference in frequency of Bax and Fas expression between each histologic category. Fas L expression was observed in one of 36 cases (3%) with adenoma, but in 12 of 33 (36%) with LPM (P< 0.001) and 42 of 63 (67%) with carcinoma (P< 0.0001). In carcinomas, cases expressing Fas L showed a less favourable prognosis than those without (P= 0.02). Density of CD8+ lymphocytes, possibly cytotoxic T-cells, was higher in serous carcinoma with negative Fas L expression than those with positive Fas L expression. These findings suggest that Fas L expressing carcinomas induce apoptosis in infiltrating CTL with Fas expression, and escape from immune surveillance. © 2000 Cancer Research Campaign |
format | Text |
id | pubmed-2363379 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2000 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23633792009-09-10 Expressions of Fas ligand and other apoptosis-related genes and their prognostic significance in epithelial ovarian neoplasms Munakata*, S Enomoto, T Tsujimoto, M Otsuki, Y Miwa, H Kanno, H Aozasa, K Br J Cancer Regular Article SummaryExpression of apoptosis-related proteins, bcl-2, Bax, Fas and Fas ligand (L), in ovarian epithelial neoplasms together with its clinical relevance was examined by immunohistochemistry. They included 36 cases with adenoma, 33 with low potential malignancy (LPM) and 63 with carcinomas. bcl-2 expression was observed in 14 of 36 cases (39%) with adenoma, five of 33 (15%) with LPM (P< 0.05) and 12 of 63 (19%) with carcinoma (P< 0.05). Cases with bcl-2 expression showed more favourable prognosis than those without, but the difference was not statistically significant. There was no difference in frequency of Bax and Fas expression between each histologic category. Fas L expression was observed in one of 36 cases (3%) with adenoma, but in 12 of 33 (36%) with LPM (P< 0.001) and 42 of 63 (67%) with carcinoma (P< 0.0001). In carcinomas, cases expressing Fas L showed a less favourable prognosis than those without (P= 0.02). Density of CD8+ lymphocytes, possibly cytotoxic T-cells, was higher in serous carcinoma with negative Fas L expression than those with positive Fas L expression. These findings suggest that Fas L expressing carcinomas induce apoptosis in infiltrating CTL with Fas expression, and escape from immune surveillance. © 2000 Cancer Research Campaign Nature Publishing Group 2000-04 2000-03-21 /pmc/articles/PMC2363379/ /pubmed/10780525 http://dx.doi.org/10.1054/bjoc.1999.1073 Text en Copyright © 2000 Cancer Research Campaign 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 | Regular Article Munakata*, S Enomoto, T Tsujimoto, M Otsuki, Y Miwa, H Kanno, H Aozasa, K Expressions of Fas ligand and other apoptosis-related genes and their prognostic significance in epithelial ovarian neoplasms |
title | Expressions of Fas ligand and other apoptosis-related genes and their prognostic significance in epithelial ovarian neoplasms |
title_full | Expressions of Fas ligand and other apoptosis-related genes and their prognostic significance in epithelial ovarian neoplasms |
title_fullStr | Expressions of Fas ligand and other apoptosis-related genes and their prognostic significance in epithelial ovarian neoplasms |
title_full_unstemmed | Expressions of Fas ligand and other apoptosis-related genes and their prognostic significance in epithelial ovarian neoplasms |
title_short | Expressions of Fas ligand and other apoptosis-related genes and their prognostic significance in epithelial ovarian neoplasms |
title_sort | expressions of fas ligand and other apoptosis-related genes and their prognostic significance in epithelial ovarian neoplasms |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363379/ https://www.ncbi.nlm.nih.gov/pubmed/10780525 http://dx.doi.org/10.1054/bjoc.1999.1073 |
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