Cargando…

Etoposide damages female germ cells in the developing ovary

BACKGROUND: As with many anti-cancer drugs, the topoisomerase II inhibitor etoposide is considered safe for administration to women in the second and third trimesters of pregnancy, but assessment of effects on the developing fetus have been limited. The purpose of this research was to examine the ef...

Descripción completa

Detalles Bibliográficos
Autores principales: Stefansdottir, Agnes, Johnston, Zoe C., Powles-Glover, Nicola, Anderson, Richard A., Adams, Ian R., Spears, Norah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4980800/
https://www.ncbi.nlm.nih.gov/pubmed/27510889
http://dx.doi.org/10.1186/s12885-016-2505-9
_version_ 1782447518910513152
author Stefansdottir, Agnes
Johnston, Zoe C.
Powles-Glover, Nicola
Anderson, Richard A.
Adams, Ian R.
Spears, Norah
author_facet Stefansdottir, Agnes
Johnston, Zoe C.
Powles-Glover, Nicola
Anderson, Richard A.
Adams, Ian R.
Spears, Norah
author_sort Stefansdottir, Agnes
collection PubMed
description BACKGROUND: As with many anti-cancer drugs, the topoisomerase II inhibitor etoposide is considered safe for administration to women in the second and third trimesters of pregnancy, but assessment of effects on the developing fetus have been limited. The purpose of this research was to examine the effect of etoposide on germ cells in the developing ovary. Mouse ovary tissue culture was used as the experimental model, thus allowing us to examine effects of etoposide on all stages of germ cell development in the same way, in vitro. RESULTS: Fetal ovaries from embryonic day 13.5 CD1 mice or neonatal ovaries from postnatal day 0 CD1 mice were cultured with 50–150 ng ml(−1) or 50–200 ng ml(−1) etoposide respectively, concentrations that are low relative to that in patient serum. When fetal ovaries were treated prior to follicle formation, etoposide resulted in dose-dependent damage, with 150 ng ml(−1) inducing a near-complete absence of healthy follicles. In contrast, treatment of neonatal ovaries, after follicle formation, had no effect on follicle numbers and only a minor effect on follicle health, even at 200 ng ml(−1). The sensitivity of female germ cells to etoposide coincided with topoisomerase IIα expression: in the developing ovary of both mouse and human, topoisomerase IIα was expressed in germ cells only prior to follicle formation. CONCLUSIONS: Exposure of pre-follicular ovaries, in which topoisomerase IIα expression was germ cell-specific, resulted in a near-complete elimination of germ cells prior to follicle formation, with the remaining germ cells going on to form unhealthy follicles by the end of culture. In contrast, exposure to follicle-enclosed oocytes, which no longer expressed topoisomerase IIα in the germ cells, had no effect on total follicle numbers or health, the only effect seen specific to transitional follicles. Results indicate the potential for adverse effects on fetal ovarian development if etoposide is administered to pregnant women when germ cells are not yet enclosed within ovarian follicles, a process that starts at approximately 17 weeks gestation and is only complete towards the end of pregnancy. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12885-016-2505-9) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-4980800
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-49808002016-08-12 Etoposide damages female germ cells in the developing ovary Stefansdottir, Agnes Johnston, Zoe C. Powles-Glover, Nicola Anderson, Richard A. Adams, Ian R. Spears, Norah BMC Cancer Research Article BACKGROUND: As with many anti-cancer drugs, the topoisomerase II inhibitor etoposide is considered safe for administration to women in the second and third trimesters of pregnancy, but assessment of effects on the developing fetus have been limited. The purpose of this research was to examine the effect of etoposide on germ cells in the developing ovary. Mouse ovary tissue culture was used as the experimental model, thus allowing us to examine effects of etoposide on all stages of germ cell development in the same way, in vitro. RESULTS: Fetal ovaries from embryonic day 13.5 CD1 mice or neonatal ovaries from postnatal day 0 CD1 mice were cultured with 50–150 ng ml(−1) or 50–200 ng ml(−1) etoposide respectively, concentrations that are low relative to that in patient serum. When fetal ovaries were treated prior to follicle formation, etoposide resulted in dose-dependent damage, with 150 ng ml(−1) inducing a near-complete absence of healthy follicles. In contrast, treatment of neonatal ovaries, after follicle formation, had no effect on follicle numbers and only a minor effect on follicle health, even at 200 ng ml(−1). The sensitivity of female germ cells to etoposide coincided with topoisomerase IIα expression: in the developing ovary of both mouse and human, topoisomerase IIα was expressed in germ cells only prior to follicle formation. CONCLUSIONS: Exposure of pre-follicular ovaries, in which topoisomerase IIα expression was germ cell-specific, resulted in a near-complete elimination of germ cells prior to follicle formation, with the remaining germ cells going on to form unhealthy follicles by the end of culture. In contrast, exposure to follicle-enclosed oocytes, which no longer expressed topoisomerase IIα in the germ cells, had no effect on total follicle numbers or health, the only effect seen specific to transitional follicles. Results indicate the potential for adverse effects on fetal ovarian development if etoposide is administered to pregnant women when germ cells are not yet enclosed within ovarian follicles, a process that starts at approximately 17 weeks gestation and is only complete towards the end of pregnancy. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12885-016-2505-9) contains supplementary material, which is available to authorized users. BioMed Central 2016-08-11 /pmc/articles/PMC4980800/ /pubmed/27510889 http://dx.doi.org/10.1186/s12885-016-2505-9 Text en © The Author(s). 2016 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 Article
Stefansdottir, Agnes
Johnston, Zoe C.
Powles-Glover, Nicola
Anderson, Richard A.
Adams, Ian R.
Spears, Norah
Etoposide damages female germ cells in the developing ovary
title Etoposide damages female germ cells in the developing ovary
title_full Etoposide damages female germ cells in the developing ovary
title_fullStr Etoposide damages female germ cells in the developing ovary
title_full_unstemmed Etoposide damages female germ cells in the developing ovary
title_short Etoposide damages female germ cells in the developing ovary
title_sort etoposide damages female germ cells in the developing ovary
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4980800/
https://www.ncbi.nlm.nih.gov/pubmed/27510889
http://dx.doi.org/10.1186/s12885-016-2505-9
work_keys_str_mv AT stefansdottiragnes etoposidedamagesfemalegermcellsinthedevelopingovary
AT johnstonzoec etoposidedamagesfemalegermcellsinthedevelopingovary
AT powlesglovernicola etoposidedamagesfemalegermcellsinthedevelopingovary
AT andersonricharda etoposidedamagesfemalegermcellsinthedevelopingovary
AT adamsianr etoposidedamagesfemalegermcellsinthedevelopingovary
AT spearsnorah etoposidedamagesfemalegermcellsinthedevelopingovary