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Topical KGF treatment as a therapeutic strategy for vaginal atrophy in a model of ovariectomized mice

One of the most frequent complaints for post-menopausal women is vaginal atrophy, because of reduction in circulating oestrogens. Treatments based on local oestrogen administration have been questioned as topic oestrogens can reach the bloodstream, thus leading to consider their safety as controvers...

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Detalles Bibliográficos
Autores principales: Ceccarelli, Simona, D'Amici, Sirio, Vescarelli, Enrica, Coluccio, Paolo, Matricardi, Pietro, di Gioia, Cira, Benedetti Panici, Pierluigi, Romano, Ferdinando, Frati, Luigi, Angeloni, Antonio, Marchese, Cinzia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4196664/
https://www.ncbi.nlm.nih.gov/pubmed/25088572
http://dx.doi.org/10.1111/jcmm.12334
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author Ceccarelli, Simona
D'Amici, Sirio
Vescarelli, Enrica
Coluccio, Paolo
Matricardi, Pietro
di Gioia, Cira
Benedetti Panici, Pierluigi
Romano, Ferdinando
Frati, Luigi
Angeloni, Antonio
Marchese, Cinzia
author_facet Ceccarelli, Simona
D'Amici, Sirio
Vescarelli, Enrica
Coluccio, Paolo
Matricardi, Pietro
di Gioia, Cira
Benedetti Panici, Pierluigi
Romano, Ferdinando
Frati, Luigi
Angeloni, Antonio
Marchese, Cinzia
author_sort Ceccarelli, Simona
collection PubMed
description One of the most frequent complaints for post-menopausal women is vaginal atrophy, because of reduction in circulating oestrogens. Treatments based on local oestrogen administration have been questioned as topic oestrogens can reach the bloodstream, thus leading to consider their safety as controversial, especially for patients with a history of breast or endometrial cancers. Recently, growth factors have been shown to interact with the oestrogen pathway, but the mechanisms still need to be fully clarified. In this study, we investigated the effect of keratinocyte growth factor (KGF), a known mitogen for epithelial cells, on human vaginal mucosa cells, and its potential crosstalk with oestrogen pathways. We also tested the in vivo efficacy of KGF local administration on vaginal atrophy in a murine model. We demonstrated that KGF is able to induce proliferation of vaginal mucosa, and we gained insight on its mechanism of action by highlighting its contribution to switch ERα signalling towards non-genomic pathway. Moreover, we demonstrated that KGF restores vaginal trophism in vivo similarly to intravaginal oestrogenic preparations, without systemic effects. Therefore, we suggest a possible alternative therapy for vaginal atrophy devoid of the risks related to oestrogen-based treatments, and a patent (no. RM2012A000404) has been applied for this study.
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spelling pubmed-41966642014-12-03 Topical KGF treatment as a therapeutic strategy for vaginal atrophy in a model of ovariectomized mice Ceccarelli, Simona D'Amici, Sirio Vescarelli, Enrica Coluccio, Paolo Matricardi, Pietro di Gioia, Cira Benedetti Panici, Pierluigi Romano, Ferdinando Frati, Luigi Angeloni, Antonio Marchese, Cinzia J Cell Mol Med Original Articles One of the most frequent complaints for post-menopausal women is vaginal atrophy, because of reduction in circulating oestrogens. Treatments based on local oestrogen administration have been questioned as topic oestrogens can reach the bloodstream, thus leading to consider their safety as controversial, especially for patients with a history of breast or endometrial cancers. Recently, growth factors have been shown to interact with the oestrogen pathway, but the mechanisms still need to be fully clarified. In this study, we investigated the effect of keratinocyte growth factor (KGF), a known mitogen for epithelial cells, on human vaginal mucosa cells, and its potential crosstalk with oestrogen pathways. We also tested the in vivo efficacy of KGF local administration on vaginal atrophy in a murine model. We demonstrated that KGF is able to induce proliferation of vaginal mucosa, and we gained insight on its mechanism of action by highlighting its contribution to switch ERα signalling towards non-genomic pathway. Moreover, we demonstrated that KGF restores vaginal trophism in vivo similarly to intravaginal oestrogenic preparations, without systemic effects. Therefore, we suggest a possible alternative therapy for vaginal atrophy devoid of the risks related to oestrogen-based treatments, and a patent (no. RM2012A000404) has been applied for this study. Blackwell Publishing Ltd 2014-09 2014-08-01 /pmc/articles/PMC4196664/ /pubmed/25088572 http://dx.doi.org/10.1111/jcmm.12334 Text en © 2014 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Ceccarelli, Simona
D'Amici, Sirio
Vescarelli, Enrica
Coluccio, Paolo
Matricardi, Pietro
di Gioia, Cira
Benedetti Panici, Pierluigi
Romano, Ferdinando
Frati, Luigi
Angeloni, Antonio
Marchese, Cinzia
Topical KGF treatment as a therapeutic strategy for vaginal atrophy in a model of ovariectomized mice
title Topical KGF treatment as a therapeutic strategy for vaginal atrophy in a model of ovariectomized mice
title_full Topical KGF treatment as a therapeutic strategy for vaginal atrophy in a model of ovariectomized mice
title_fullStr Topical KGF treatment as a therapeutic strategy for vaginal atrophy in a model of ovariectomized mice
title_full_unstemmed Topical KGF treatment as a therapeutic strategy for vaginal atrophy in a model of ovariectomized mice
title_short Topical KGF treatment as a therapeutic strategy for vaginal atrophy in a model of ovariectomized mice
title_sort topical kgf treatment as a therapeutic strategy for vaginal atrophy in a model of ovariectomized mice
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4196664/
https://www.ncbi.nlm.nih.gov/pubmed/25088572
http://dx.doi.org/10.1111/jcmm.12334
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