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Inducing malignant transformation of endometriosis in rats by long-term sustaining hyperestrogenemia and type II diabetes

This study aimed to induce malignant transformation of endometriosis in Sprague–Dawley rats by hyperestrogenemia and type II diabetes and evaluate its similarity with human disease in biological features. Rats with surgically induced endometriosis were randomized into two groups: those treated with...

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Autores principales: Wang, Chang-Ting, Wang, Dan-Bo, Liu, Kui-Ran, Li, Yan, Sun, Chun-Xiao, Guo, Cui-Shan, Ren, Fang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BlackWell Publishing Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4317770/
https://www.ncbi.nlm.nih.gov/pubmed/25421527
http://dx.doi.org/10.1111/cas.12573
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author Wang, Chang-Ting
Wang, Dan-Bo
Liu, Kui-Ran
Li, Yan
Sun, Chun-Xiao
Guo, Cui-Shan
Ren, Fang
author_facet Wang, Chang-Ting
Wang, Dan-Bo
Liu, Kui-Ran
Li, Yan
Sun, Chun-Xiao
Guo, Cui-Shan
Ren, Fang
author_sort Wang, Chang-Ting
collection PubMed
description This study aimed to induce malignant transformation of endometriosis in Sprague–Dawley rats by hyperestrogenemia and type II diabetes and evaluate its similarity with human disease in biological features. Rats with surgically induced endometriosis were randomized into two groups: those treated with estradiol (5 mg/kg three times/week after surgery), streptozotocin (25 mg/kg, 1 month after surgery), and high carbohydrate-and-fat feed (Es group); and those treated with placebo saline and standard feed (control group). All rats were randomly killed 2, 4, or 8 months after surgery. The endometriosis lesions and the corresponding eutopic endometria were subjected to morphological evaluation, TUNEL, and immunohistochemical analysis for the expressions of proliferating cell nuclear antigen, phosphatase and tensin homolog, phosphorylated protein kinase B, and phosphorylated mammalian target of rapamycin proteins. In the Es group, three cases (6.0%) of endometriosis showed atypical hyperplasia accompanied by simple hyperplastic eutopic endometria, and two cases (4.0%) of endometriosis showed endometrioid carcinoma accompanied by atypical hyperplastic eutopic endometria. In the Es group, the activity of organelles and the expressions of proliferating cell nuclear antigen, phosphorylated protein kinase B, and phosphorylated mammalian target of rapamycin increased, and the level of phosphatase and tensin homolog and TUNEL positivity decreased progressively in the order of endometriosis, atypical endometriosis, and malignant endometriosis. The same tendency was found in the corresponding eutopic endometria. The induced malignant endometriosis showed similarities with human disease in the pathological process and histomorphological and molecular biological features. The method is feasible. The malignant transformations of endometriosis and eutopic endometria may have correlations and similarities, but the former may suffer a higher risk of canceration.
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spelling pubmed-43177702015-10-05 Inducing malignant transformation of endometriosis in rats by long-term sustaining hyperestrogenemia and type II diabetes Wang, Chang-Ting Wang, Dan-Bo Liu, Kui-Ran Li, Yan Sun, Chun-Xiao Guo, Cui-Shan Ren, Fang Cancer Sci Original Articles This study aimed to induce malignant transformation of endometriosis in Sprague–Dawley rats by hyperestrogenemia and type II diabetes and evaluate its similarity with human disease in biological features. Rats with surgically induced endometriosis were randomized into two groups: those treated with estradiol (5 mg/kg three times/week after surgery), streptozotocin (25 mg/kg, 1 month after surgery), and high carbohydrate-and-fat feed (Es group); and those treated with placebo saline and standard feed (control group). All rats were randomly killed 2, 4, or 8 months after surgery. The endometriosis lesions and the corresponding eutopic endometria were subjected to morphological evaluation, TUNEL, and immunohistochemical analysis for the expressions of proliferating cell nuclear antigen, phosphatase and tensin homolog, phosphorylated protein kinase B, and phosphorylated mammalian target of rapamycin proteins. In the Es group, three cases (6.0%) of endometriosis showed atypical hyperplasia accompanied by simple hyperplastic eutopic endometria, and two cases (4.0%) of endometriosis showed endometrioid carcinoma accompanied by atypical hyperplastic eutopic endometria. In the Es group, the activity of organelles and the expressions of proliferating cell nuclear antigen, phosphorylated protein kinase B, and phosphorylated mammalian target of rapamycin increased, and the level of phosphatase and tensin homolog and TUNEL positivity decreased progressively in the order of endometriosis, atypical endometriosis, and malignant endometriosis. The same tendency was found in the corresponding eutopic endometria. The induced malignant endometriosis showed similarities with human disease in the pathological process and histomorphological and molecular biological features. The method is feasible. The malignant transformations of endometriosis and eutopic endometria may have correlations and similarities, but the former may suffer a higher risk of canceration. BlackWell Publishing Ltd 2015-01 2014-12-18 /pmc/articles/PMC4317770/ /pubmed/25421527 http://dx.doi.org/10.1111/cas.12573 Text en © 2014 The Authors. Cancer Science published by Wiley Publishing Asia Pty Ltd on behalf of Japanese Cancer Association. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, 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 Original Articles
Wang, Chang-Ting
Wang, Dan-Bo
Liu, Kui-Ran
Li, Yan
Sun, Chun-Xiao
Guo, Cui-Shan
Ren, Fang
Inducing malignant transformation of endometriosis in rats by long-term sustaining hyperestrogenemia and type II diabetes
title Inducing malignant transformation of endometriosis in rats by long-term sustaining hyperestrogenemia and type II diabetes
title_full Inducing malignant transformation of endometriosis in rats by long-term sustaining hyperestrogenemia and type II diabetes
title_fullStr Inducing malignant transformation of endometriosis in rats by long-term sustaining hyperestrogenemia and type II diabetes
title_full_unstemmed Inducing malignant transformation of endometriosis in rats by long-term sustaining hyperestrogenemia and type II diabetes
title_short Inducing malignant transformation of endometriosis in rats by long-term sustaining hyperestrogenemia and type II diabetes
title_sort inducing malignant transformation of endometriosis in rats by long-term sustaining hyperestrogenemia and type ii diabetes
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4317770/
https://www.ncbi.nlm.nih.gov/pubmed/25421527
http://dx.doi.org/10.1111/cas.12573
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