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Published on: June 23, 2023
Etoposide damages female germ cells in the developing ovary
Agnes Stefansdottir1, Zoe C Johnston1,2, Nicola Powles-Glover3
1Centre for Integrative Physiology, University of Edinburgh, Edinburgh, EH8 9XD, UK.
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.
Insights
Etoposide exposure before follicle formation in fetal ovaries causes significant germ cell damage. Ovarian germ cells are sensitive to etoposide only before they are enclosed within follicles.
Area of Science:
- Reproductive Biology
- Developmental Biology
- Toxicology
Background:
- Etoposide, a topoisomerase II inhibitor, is used as an anti-cancer drug.
- Its safety during pregnancy is assumed for the second and third trimesters, but fetal effects are not well-assessed.
- Limited data exists on etoposide's impact on fetal ovarian development.
Purpose of the Study:
- To investigate the effects of etoposide on germ cells in the developing ovary.
- To determine the sensitivity of ovarian germ cells to etoposide at different developmental stages.
Main Methods:
- Mouse ovary tissue culture was utilized as an in vitro experimental model.
- Fetal and neonatal mouse ovaries were cultured with varying concentrations of etoposide.
- Ovaries were treated before and after follicle formation to assess differential sensitivity.
Main Results:
- Etoposide exposure to pre-follicular ovaries caused dose-dependent germ cell damage and reduced healthy follicle formation.
- Neonatal ovaries treated after follicle formation showed minimal effects on follicle number and health.
- Germ cell sensitivity to etoposide correlated with topoisomerase IIα expression, which was present only before follicle formation.
Conclusions:
- Etoposide can cause severe damage to fetal ovarian germ cells if administered before follicle enclosure.
- Ovarian germ cells are protected from etoposide's adverse effects once enclosed within follicles.
- Clinical use of etoposide during pregnancy requires careful consideration of gestational timing relative to ovarian follicle development.
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