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Spontaneous antral follicle formation and metaphase II oocyte from a non-stimulated prepubertal ovarian tissue xenotransplant

BACKGROUND: Current strategies in cancer treatment have markedly increased the rates of remission and survival for cancer patients, but are often associated with subsequent sterility. While there are various options available to an adult female depending on the patient’s particular situation, the on...

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Autores principales: Lotz, Laura, Liebenthron, Jana, Nichols-Burns, Stephanie M, Montag, Markus, Hoffmann, Inge, Beckmann, Matthias W, van der Ven, Hans, Töpfer, Dagmar, Dittrich, Ralf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4036711/
https://www.ncbi.nlm.nih.gov/pubmed/24886634
http://dx.doi.org/10.1186/1477-7827-12-41
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author Lotz, Laura
Liebenthron, Jana
Nichols-Burns, Stephanie M
Montag, Markus
Hoffmann, Inge
Beckmann, Matthias W
van der Ven, Hans
Töpfer, Dagmar
Dittrich, Ralf
author_facet Lotz, Laura
Liebenthron, Jana
Nichols-Burns, Stephanie M
Montag, Markus
Hoffmann, Inge
Beckmann, Matthias W
van der Ven, Hans
Töpfer, Dagmar
Dittrich, Ralf
author_sort Lotz, Laura
collection PubMed
description BACKGROUND: Current strategies in cancer treatment have markedly increased the rates of remission and survival for cancer patients, but are often associated with subsequent sterility. While there are various options available to an adult female depending on the patient’s particular situation, the only realistic option for preserving fertility in prepubertal females is to cryopreserve ovarian tissue. This is the first report of a morphologically mature oocyte collected from non-stimulated prepubertal ovarian tissue xenotransplants. METHODS: Ovarian tissue from a 6 year old patient suffering from nephroblastoma was removed and cryopreserved for fertility preservation. The frozen-thawed ovarian tissue fragments were xenotransplanted to bilaterally oophorectomized severe combined immunodeficiency (SCID) mice to assess follicle development. RESULTS: Antral follicle formation occurred post-xenotransplantation in a single ovarian fragment without exogenous hormone stimulation. A morphologically maturing oocyte was harvested from these follicles. CONCLUSIONS: Prepubertal human ovarian follicles and oocytes can be matured after xenotransplantation even without exogenous hormone stimulation. These results indicate that tissue collected from prepubertal patients can support fertility in cancer survivors.
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spelling pubmed-40367112014-05-29 Spontaneous antral follicle formation and metaphase II oocyte from a non-stimulated prepubertal ovarian tissue xenotransplant Lotz, Laura Liebenthron, Jana Nichols-Burns, Stephanie M Montag, Markus Hoffmann, Inge Beckmann, Matthias W van der Ven, Hans Töpfer, Dagmar Dittrich, Ralf Reprod Biol Endocrinol Research BACKGROUND: Current strategies in cancer treatment have markedly increased the rates of remission and survival for cancer patients, but are often associated with subsequent sterility. While there are various options available to an adult female depending on the patient’s particular situation, the only realistic option for preserving fertility in prepubertal females is to cryopreserve ovarian tissue. This is the first report of a morphologically mature oocyte collected from non-stimulated prepubertal ovarian tissue xenotransplants. METHODS: Ovarian tissue from a 6 year old patient suffering from nephroblastoma was removed and cryopreserved for fertility preservation. The frozen-thawed ovarian tissue fragments were xenotransplanted to bilaterally oophorectomized severe combined immunodeficiency (SCID) mice to assess follicle development. RESULTS: Antral follicle formation occurred post-xenotransplantation in a single ovarian fragment without exogenous hormone stimulation. A morphologically maturing oocyte was harvested from these follicles. CONCLUSIONS: Prepubertal human ovarian follicles and oocytes can be matured after xenotransplantation even without exogenous hormone stimulation. These results indicate that tissue collected from prepubertal patients can support fertility in cancer survivors. BioMed Central 2014-05-15 /pmc/articles/PMC4036711/ /pubmed/24886634 http://dx.doi.org/10.1186/1477-7827-12-41 Text en Copyright © 2014 Lotz et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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
Lotz, Laura
Liebenthron, Jana
Nichols-Burns, Stephanie M
Montag, Markus
Hoffmann, Inge
Beckmann, Matthias W
van der Ven, Hans
Töpfer, Dagmar
Dittrich, Ralf
Spontaneous antral follicle formation and metaphase II oocyte from a non-stimulated prepubertal ovarian tissue xenotransplant
title Spontaneous antral follicle formation and metaphase II oocyte from a non-stimulated prepubertal ovarian tissue xenotransplant
title_full Spontaneous antral follicle formation and metaphase II oocyte from a non-stimulated prepubertal ovarian tissue xenotransplant
title_fullStr Spontaneous antral follicle formation and metaphase II oocyte from a non-stimulated prepubertal ovarian tissue xenotransplant
title_full_unstemmed Spontaneous antral follicle formation and metaphase II oocyte from a non-stimulated prepubertal ovarian tissue xenotransplant
title_short Spontaneous antral follicle formation and metaphase II oocyte from a non-stimulated prepubertal ovarian tissue xenotransplant
title_sort spontaneous antral follicle formation and metaphase ii oocyte from a non-stimulated prepubertal ovarian tissue xenotransplant
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4036711/
https://www.ncbi.nlm.nih.gov/pubmed/24886634
http://dx.doi.org/10.1186/1477-7827-12-41
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