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DNA topoisomerase IIα and -β expression in human ovarian cancer
To study DNA topoisomerase IIα (Topo-IIα) and -β expression and regulation in human ovarian cancer, 15 ovarian tumour samples were investigated. To compare different levels of expression, the samples were screened for topo IIα and -β mRNA with Northern blotting and a quantitative reverse transcripta...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
1999
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2362692/ https://www.ncbi.nlm.nih.gov/pubmed/10070864 http://dx.doi.org/10.1038/sj.bjc.6690120 |
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author | Withoff, S Zee, A G J van der Jong, S de Hollema, H Smit, E F Mulder, N H Vries, E G E de |
author_facet | Withoff, S Zee, A G J van der Jong, S de Hollema, H Smit, E F Mulder, N H Vries, E G E de |
author_sort | Withoff, S |
collection | PubMed |
description | To study DNA topoisomerase IIα (Topo-IIα) and -β expression and regulation in human ovarian cancer, 15 ovarian tumour samples were investigated. To compare different levels of expression, the samples were screened for topo IIα and -β mRNA with Northern blotting and a quantitative reverse transcriptase polymerase chain reaction (RT-PCR) assay for Topo-IIα mRNA. Additionally, protein levels were determined with Western blotting and topoisomerase II activity levels with the decatenation assay. The results obtained were compared with each other and with the tumour volume index of the samples. In tumours with a tumour volume index ≥ 50%, the mRNA levels (as determined by Northern blotting) and protein levels for each isozyme were in accordance. Additionally, correlations were found between Topo-IIα RT-PCR data and Topo-IIα Northern blot results, and between Topo-IIα RT-PCR data and Topo-IIα protein levels. Interestingly, Topo-IIβ protein levels correlated better with Topo-II activity than Topo-IIα protein levels. In eight ovarian cystadenoma samples, no Topo-IIα protein could be found. In only three out of eight of these cystadenomas, Topo-IIβ protein could be detected. These findings suggest that Topo-IIα and Topo-IIβ protein levels are up-regulated in ovarian cancer and may indicate that Topo-IIβ is an interesting target for chemotherapy in ovarian tumours. © 1999 Cancer Research Campaign |
format | Text |
id | pubmed-2362692 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1999 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23626922009-09-10 DNA topoisomerase IIα and -β expression in human ovarian cancer Withoff, S Zee, A G J van der Jong, S de Hollema, H Smit, E F Mulder, N H Vries, E G E de Br J Cancer Regular Article To study DNA topoisomerase IIα (Topo-IIα) and -β expression and regulation in human ovarian cancer, 15 ovarian tumour samples were investigated. To compare different levels of expression, the samples were screened for topo IIα and -β mRNA with Northern blotting and a quantitative reverse transcriptase polymerase chain reaction (RT-PCR) assay for Topo-IIα mRNA. Additionally, protein levels were determined with Western blotting and topoisomerase II activity levels with the decatenation assay. The results obtained were compared with each other and with the tumour volume index of the samples. In tumours with a tumour volume index ≥ 50%, the mRNA levels (as determined by Northern blotting) and protein levels for each isozyme were in accordance. Additionally, correlations were found between Topo-IIα RT-PCR data and Topo-IIα Northern blot results, and between Topo-IIα RT-PCR data and Topo-IIα protein levels. Interestingly, Topo-IIβ protein levels correlated better with Topo-II activity than Topo-IIα protein levels. In eight ovarian cystadenoma samples, no Topo-IIα protein could be found. In only three out of eight of these cystadenomas, Topo-IIβ protein could be detected. These findings suggest that Topo-IIα and Topo-IIβ protein levels are up-regulated in ovarian cancer and may indicate that Topo-IIβ is an interesting target for chemotherapy in ovarian tumours. © 1999 Cancer Research Campaign Nature Publishing Group 1999-02 /pmc/articles/PMC2362692/ /pubmed/10070864 http://dx.doi.org/10.1038/sj.bjc.6690120 Text en Copyright © 1999 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 Withoff, S Zee, A G J van der Jong, S de Hollema, H Smit, E F Mulder, N H Vries, E G E de DNA topoisomerase IIα and -β expression in human ovarian cancer |
title | DNA topoisomerase IIα and -β expression in human ovarian cancer |
title_full | DNA topoisomerase IIα and -β expression in human ovarian cancer |
title_fullStr | DNA topoisomerase IIα and -β expression in human ovarian cancer |
title_full_unstemmed | DNA topoisomerase IIα and -β expression in human ovarian cancer |
title_short | DNA topoisomerase IIα and -β expression in human ovarian cancer |
title_sort | dna topoisomerase iiα and -β expression in human ovarian cancer |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2362692/ https://www.ncbi.nlm.nih.gov/pubmed/10070864 http://dx.doi.org/10.1038/sj.bjc.6690120 |
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