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Follicle Rescue From Prepubertal Ovaries After Recent Treatment With Cyclophosphamide-An Experimental Culture System Using Mice to Achieve Mature Oocytes for Fertility Preservation

Overview
Journal Front Oncol
Specialty Oncology
Date 2021 Oct 11
PMID 34631518
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Abstract

Ovarian tissue cryopreservation is the only feasible method for fertility preservation in prepubertal girls that will undergo gonadotoxic chemotherapy. To date, the only clinical use of cryopreserved tissue is by a later tissue retransplantation to the patient. Clinical challenges in fertility preservation of very young patients with cancer include time constraints that do not allow to retrieve the tissue for cryopreservation before starting chemotherapy and the preclusion of future ovarian tissue transplantation due to the risk of reintroduction of malignant cells in patients with systemic diseases. To overcome these two challenges, we investigated using an experimental model the feasibility of retrieving secondary follicles from ovaries of prepubertal mice after cyclophosphamide (CPA) treatment in increasing doses of 50, 75, and 100 mg/kg. The follicles were thereafter cultured and matured . The main outcomes included the efficiency of the method in terms of obtained matured oocytes and the safety of these potentially fertility preservative procedures in terms of analyses of oocyte competence regarding normality of the spindle and chromosome configurations. Our findings demonstrated that it was feasible to isolate and culture secondary follicles and to obtain mature oocytes from prepubertal mice ovaries recently treated with CPA. The efficiency of this method was highly demonstrated in the 100 mg/kg CPA group, with near 90% follicle survival rate after 12 days' culture, similarly to control. Around 80% of the follicles met the criteria to put into maturation, and more than 40% of them achieved metaphase II, with normal spindle and chromosome configurations observed. Suboptimal results were obtained in the 50 and 75 mg/kg CPA groups. These paradoxical findings towards CPA dose might probably reflect a more difficult selection of damaged growing follicles from ovaries recently treated with lower doses of CPA and a hampered ability to identify and discard those with reduced viability for the culture.

References
1.
Visser J, Themmen A . Role of anti-Müllerian hormone and bone morphogenetic proteins in the regulation of FSH sensitivity. Mol Cell Endocrinol. 2013; 382(1):460-465. DOI: 10.1016/j.mce.2013.08.012. View

2.
Anastacio A, Waterstone M, Hao X, Poirot C, Rodriguez-Wallberg K . Ovarian Follicles Rescued 3 Days after Cyclophosphamide Treatment in Adolescent Mice: An Experimental Study Aiming at Maximizing Methods for Fertility Preservation through In Vitro Follicle Culture. Int J Mol Sci. 2019; 20(24). PMC: 6940762. DOI: 10.3390/ijms20246190. View

3.
Anastacio A, Rodriguez-Wallberg K, Chardonnet S, Pionneau C, Federici C, Almeida Santos T . Protein profile of mouse ovarian follicles grown in vitro. Mol Hum Reprod. 2017; 23(12):827-841. PMC: 5909860. DOI: 10.1093/molehr/gax056. View

4.
Rodriguez-Wallberg K, Milenkovic M, Papaikonomou K, Keros V, Gustafsson B, Sergouniotis F . Successful pregnancies after transplantation of ovarian tissue retrieved and cryopreserved at time of childhood acute lymphoblastic leukemia - A case report. Haematologica. 2021; 106(10):2783-2787. PMC: 8485665. DOI: 10.3324/haematol.2021.278828. View

5.
Salian S, Uppangala S, Cheredath A, DSouza F, Kalthur G, Nayak V . Early prepubertal cyclophosphamide exposure in mice results in long-term loss of ovarian reserve, and impaired embryonic development and blastocyst quality. PLoS One. 2020; 15(6):e0235140. PMC: 7310698. DOI: 10.1371/journal.pone.0235140. View