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Cyclin A is a reliable proliferation marker in endometrial cancer cell lines
Cyclin A, a cell cycle regulatory protein, promotes cell proliferation and has been observed to be highly expressed in cancer and to promote tumor growth; however, its value as a marker for endometrial carcinoma has not yet been established. Accordingly, the aim of the present study was to clarify w...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6447861/ https://www.ncbi.nlm.nih.gov/pubmed/30988814 http://dx.doi.org/10.3892/ol.2019.10135 |
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author | Horie, Kayo Yamamoto, Hayate Karube, Kouhei Takebayashi, Kai Yoshino, Hironori Yoshioka, Haruhiko Watanabe, Jun |
author_facet | Horie, Kayo Yamamoto, Hayate Karube, Kouhei Takebayashi, Kai Yoshino, Hironori Yoshioka, Haruhiko Watanabe, Jun |
author_sort | Horie, Kayo |
collection | PubMed |
description | Cyclin A, a cell cycle regulatory protein, promotes cell proliferation and has been observed to be highly expressed in cancer and to promote tumor growth; however, its value as a marker for endometrial carcinoma has not yet been established. Accordingly, the aim of the present study was to clarify whether cyclin A can be used as a cell proliferation marker using the endometrial carcinoma cell lines Ishikawa and HEC-50B, derived from patients with low-grade and high-grade cancer, respectively. The expression of cyclin A was determined by flow cytometry using double staining with FITC and 7-AAD, and immunocytochemical staining. The results were compared to those of Ki-67, the widely used cell proliferation marker that is considered to be a prognostic marker in endometrial cancer. The flow cytometry results revealed that cyclin A expression was significantly higher in HEC-50B than in Ishikawa cells during the logarithmic growth phase. In addition, cyclin A expression was consistently higher than Ki-67 expression in the examined cell lines. Immunocytochemical staining confirmed cyclin A expression in HEC-50B and Ishikawa cells, demonstrating significantly higher expression during the logarithmic growth phase than during the stationary phase. By contrast, Ki-67 was expressed in almost 90% of the cells, irrespective of their growth state. These results indicate that cyclin A expression is significantly increased in cells with higher proliferative ability and is specifically expressed in cells that have passed the G1-S checkpoint. Therefore, cyclin A may be a reliable proliferation biomarker for endometrioid carcinoma. |
format | Online Article Text |
id | pubmed-6447861 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-64478612019-04-15 Cyclin A is a reliable proliferation marker in endometrial cancer cell lines Horie, Kayo Yamamoto, Hayate Karube, Kouhei Takebayashi, Kai Yoshino, Hironori Yoshioka, Haruhiko Watanabe, Jun Oncol Lett Articles Cyclin A, a cell cycle regulatory protein, promotes cell proliferation and has been observed to be highly expressed in cancer and to promote tumor growth; however, its value as a marker for endometrial carcinoma has not yet been established. Accordingly, the aim of the present study was to clarify whether cyclin A can be used as a cell proliferation marker using the endometrial carcinoma cell lines Ishikawa and HEC-50B, derived from patients with low-grade and high-grade cancer, respectively. The expression of cyclin A was determined by flow cytometry using double staining with FITC and 7-AAD, and immunocytochemical staining. The results were compared to those of Ki-67, the widely used cell proliferation marker that is considered to be a prognostic marker in endometrial cancer. The flow cytometry results revealed that cyclin A expression was significantly higher in HEC-50B than in Ishikawa cells during the logarithmic growth phase. In addition, cyclin A expression was consistently higher than Ki-67 expression in the examined cell lines. Immunocytochemical staining confirmed cyclin A expression in HEC-50B and Ishikawa cells, demonstrating significantly higher expression during the logarithmic growth phase than during the stationary phase. By contrast, Ki-67 was expressed in almost 90% of the cells, irrespective of their growth state. These results indicate that cyclin A expression is significantly increased in cells with higher proliferative ability and is specifically expressed in cells that have passed the G1-S checkpoint. Therefore, cyclin A may be a reliable proliferation biomarker for endometrioid carcinoma. D.A. Spandidos 2019-05 2019-03-08 /pmc/articles/PMC6447861/ /pubmed/30988814 http://dx.doi.org/10.3892/ol.2019.10135 Text en Copyright: © Horie et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Horie, Kayo Yamamoto, Hayate Karube, Kouhei Takebayashi, Kai Yoshino, Hironori Yoshioka, Haruhiko Watanabe, Jun Cyclin A is a reliable proliferation marker in endometrial cancer cell lines |
title | Cyclin A is a reliable proliferation marker in endometrial cancer cell lines |
title_full | Cyclin A is a reliable proliferation marker in endometrial cancer cell lines |
title_fullStr | Cyclin A is a reliable proliferation marker in endometrial cancer cell lines |
title_full_unstemmed | Cyclin A is a reliable proliferation marker in endometrial cancer cell lines |
title_short | Cyclin A is a reliable proliferation marker in endometrial cancer cell lines |
title_sort | cyclin a is a reliable proliferation marker in endometrial cancer cell lines |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6447861/ https://www.ncbi.nlm.nih.gov/pubmed/30988814 http://dx.doi.org/10.3892/ol.2019.10135 |
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