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BRCA1 expression, proliferative and apoptotic activities in ovarian epithelial inclusions

BACKGROUND: The purpose of this study was to examine proliferative and apoptotic activity in relation with BRCA1 expression in ovarian epithelial inclusions (OEIs), the putative precursor lesions of ovarian epithelial cancer (OEC). METHODS: Benign ovaries from 95 patients were examined. Dual immunoh...

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Autores principales: Wang, Yiying, Wang, Yue, Wei, Li, Hong, Shuhui, Zhao, Miaoqing, Zhang, Xi, Zheng, Wenxin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5341199/
https://www.ncbi.nlm.nih.gov/pubmed/28270171
http://dx.doi.org/10.1186/s13048-017-0307-6
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author Wang, Yiying
Wang, Yue
Wei, Li
Hong, Shuhui
Zhao, Miaoqing
Zhang, Xi
Zheng, Wenxin
author_facet Wang, Yiying
Wang, Yue
Wei, Li
Hong, Shuhui
Zhao, Miaoqing
Zhang, Xi
Zheng, Wenxin
author_sort Wang, Yiying
collection PubMed
description BACKGROUND: The purpose of this study was to examine proliferative and apoptotic activity in relation with BRCA1 expression in ovarian epithelial inclusions (OEIs), the putative precursor lesions of ovarian epithelial cancer (OEC). METHODS: Benign ovaries from 95 patients were examined. Dual immunohistochemical staining for both BRCA1 and MIB-1 were performed to examine the relationship between BRCA1 and MIB-1 in OEI cells. Apoptotic activity was assessed on the parallel tissue sections by using TUNEL assay. Patients’ age, menstrual phase and menopausal status were analyzed. RESULTS: OEIs were present in the ovaries of 53% of the patients. OEIs were less frequently found in premenopausal (45%) than postmenopausal women (58%). BRCA1 and MIB-1 were found in 27 and 47% of the OEI-containing ovaries, respectively. All BRCA1 positive OEI cells are MIB-1 positive with dual staining method, although overall the percentage of positive cells was small. No significant difference was found for BRCA1 and MIB-1 expression in OEIs between menopausal status and menstrual phases. Apoptosis containing OEIs were seen in 70% of the ovaries. Compared to OEIs in proliferative menstrual phase and premenopausal status, significantly more apoptosis was found in OEIs from secretory phase and postmenopausal women. A small fraction of the epithelial cells within OEIs are proliferating or dying. CONCLUSIONS: Low estrogen and/or high progesterone levels may promote OEI cell turnover via induction of apoptosis. Imbalance between cell proliferation and death within OEIs under influence of hormones may play a role in the ovarian epithelial tumorigenesis.
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spelling pubmed-53411992017-03-10 BRCA1 expression, proliferative and apoptotic activities in ovarian epithelial inclusions Wang, Yiying Wang, Yue Wei, Li Hong, Shuhui Zhao, Miaoqing Zhang, Xi Zheng, Wenxin J Ovarian Res Research BACKGROUND: The purpose of this study was to examine proliferative and apoptotic activity in relation with BRCA1 expression in ovarian epithelial inclusions (OEIs), the putative precursor lesions of ovarian epithelial cancer (OEC). METHODS: Benign ovaries from 95 patients were examined. Dual immunohistochemical staining for both BRCA1 and MIB-1 were performed to examine the relationship between BRCA1 and MIB-1 in OEI cells. Apoptotic activity was assessed on the parallel tissue sections by using TUNEL assay. Patients’ age, menstrual phase and menopausal status were analyzed. RESULTS: OEIs were present in the ovaries of 53% of the patients. OEIs were less frequently found in premenopausal (45%) than postmenopausal women (58%). BRCA1 and MIB-1 were found in 27 and 47% of the OEI-containing ovaries, respectively. All BRCA1 positive OEI cells are MIB-1 positive with dual staining method, although overall the percentage of positive cells was small. No significant difference was found for BRCA1 and MIB-1 expression in OEIs between menopausal status and menstrual phases. Apoptosis containing OEIs were seen in 70% of the ovaries. Compared to OEIs in proliferative menstrual phase and premenopausal status, significantly more apoptosis was found in OEIs from secretory phase and postmenopausal women. A small fraction of the epithelial cells within OEIs are proliferating or dying. CONCLUSIONS: Low estrogen and/or high progesterone levels may promote OEI cell turnover via induction of apoptosis. Imbalance between cell proliferation and death within OEIs under influence of hormones may play a role in the ovarian epithelial tumorigenesis. BioMed Central 2017-03-07 /pmc/articles/PMC5341199/ /pubmed/28270171 http://dx.doi.org/10.1186/s13048-017-0307-6 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Wang, Yiying
Wang, Yue
Wei, Li
Hong, Shuhui
Zhao, Miaoqing
Zhang, Xi
Zheng, Wenxin
BRCA1 expression, proliferative and apoptotic activities in ovarian epithelial inclusions
title BRCA1 expression, proliferative and apoptotic activities in ovarian epithelial inclusions
title_full BRCA1 expression, proliferative and apoptotic activities in ovarian epithelial inclusions
title_fullStr BRCA1 expression, proliferative and apoptotic activities in ovarian epithelial inclusions
title_full_unstemmed BRCA1 expression, proliferative and apoptotic activities in ovarian epithelial inclusions
title_short BRCA1 expression, proliferative and apoptotic activities in ovarian epithelial inclusions
title_sort brca1 expression, proliferative and apoptotic activities in ovarian epithelial inclusions
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5341199/
https://www.ncbi.nlm.nih.gov/pubmed/28270171
http://dx.doi.org/10.1186/s13048-017-0307-6
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