Literature DB >> 16010414

Apoptosis in cryopreserved human ovarian tissue obtained from cancer patients: a tool for evaluating cryopreservation utility.

E Rimon1, T Cohen, A Dantes, L Hirsh, A Amit, J B Lessing, S Freimann, A Amsterdam, F Azem.   

Abstract

Fertility preservation is of major importance for women with cancer in whom ovarian function may be disturbed by the use of potentially sterilizing chemotherapeutic drugs and/or pelvic irradiation. Cryopreservation of ovarian cortical tissue is one of the potential options for preserving fertility among these women. Cryopreserved thawed human ovarian tissue can be autografted either orthotopically or heterotopically, but may also be transplanted first into an animal host with subsequent maturation and collection of oocytes. The objective of this study was to investigate the prevalence of ovarian follicular apoptosis in fresh and frozen/ thawed human ovarian tissue as a measure of follicular viability. The study group included 6 women with cancer who underwent ovarian tissue cryopreservation (OTCP). Ovarian tissue samples (n = 2) were obtained from each woman with one sample undergoing evaluation for apoptosis immediately following removal (control, group A) and the other evaluated for apoptosis following freezing/thawing (group B). Terminal deoxynucleotidyl transferase-mediated deoxyuridine triphosphate nick end-labeling (TUNEL) and 4'6' diamido-2-phenylindole hydrochloride (DAPI) staining methods were used to investigate follicular apoptosis. Morphological changes in the same samples were evaluated in hematoxylin and eosin (H&E)-stained sections. In each slide, only primordial and primary follicles were evaluated for abnormal morphology and apoptosis. Abnormal morphology was demonstrated in 23.8+/-8.7% of group A follicles compared to 48.3+/-11.2% of group B follicles (p < 0.05). Apoptosis was demonstrated in 25.4+/-8.4% of group A follicles compared to 60.9+/-6.0% of group B follicles (p < 0.05). We have shown that the ovarian follicles in group B demonstrated a higher incidence of apoptosis compared to those of group A. Therefore, the data suggest that follicular apoptosis might be a consequence of the freezing and thawing procedure. This may be used as a method for evaluating and comparing the outcome of different freezing/thawing protocols.

Entities:  

Mesh:

Substances:

Year:  2005        PMID: 16010414     DOI: 10.3892/ijo.27.2.345

Source DB:  PubMed          Journal:  Int J Oncol        ISSN: 1019-6439            Impact factor:   5.650


  13 in total

1.  Efficacy of ovarian tissue cryopreservation in a major European center.

Authors:  L Bastings; J Liebenthron; J R Westphal; C C M Beerendonk; H van der Ven; B Meinecke; M Montag; D D M Braat; R Peek
Journal:  J Assist Reprod Genet       Date:  2014-06-14       Impact factor: 3.412

2.  Successful vitrification of mouse ovaries using less-concentrated cryoprotectants with Supercool X-1000 supplementation.

Authors:  Xiuwen Tan; Enliang Song; Xiaomu Liu; Guifen Liu; Haijian Cheng; Fachun Wan
Journal:  In Vitro Cell Dev Biol Anim       Date:  2012-01-11       Impact factor: 2.416

3.  Is caspase inhibition a valid therapeutic strategy in cryopreservation of ovarian tissue?

Authors:  Jian-Min Zhang; Lin-Xia Li; Yi-Xia Yang; Xue-Lian Liu; Xiao-Ping Wan
Journal:  J Assist Reprod Genet       Date:  2009-08-21       Impact factor: 3.412

4.  Quality and functionality of human ovarian tissue after cryopreservation using an original slow freezing procedure.

Authors:  Sandra Sanfilippo; Michel Canis; Sergio Romero; Benoît Sion; Pierre Déchelotte; Jean-Luc Pouly; Laurent Janny; Johan Smitz; Florence Brugnon
Journal:  J Assist Reprod Genet       Date:  2012-12-22       Impact factor: 3.412

5.  Examination of viability and quality of ovarian tissue after cryopreservation using simple laboratory methods in ewe.

Authors:  Ghaya Merdassi; Claire Mazoyer; Jean F Guerin; Ali Saad; Bruno Salle; Jacqueline Lornage
Journal:  Reprod Biol Endocrinol       Date:  2011-06-08       Impact factor: 5.211

6.  Morphology and function of cryopreserved whole ovine ovaries after heterotopic autotransplantation.

Authors:  Anna T Grazul-Bilska; Jashoman Banerjee; Ilker Yazici; Ewa Borowczyk; Jerzy J Bilski; Rakesh K Sharma; Maria Siemionov; Tommaso Falcone
Journal:  Reprod Biol Endocrinol       Date:  2008-04-11       Impact factor: 5.211

7.  Supplementation of transport and freezing media with anti-apoptotic drugs improves ovarian cortex survival.

Authors:  Laurie Henry; Maïté Fransolet; Soraya Labied; Silvia Blacher; Marie-Caroline Masereel; Jean-Michel Foidart; Agnès Noel; Michelle Nisolle; Carine Munaut
Journal:  J Ovarian Res       Date:  2016-02-12       Impact factor: 4.234

Review 8.  Molecular Basis Associated with the Control of Primordial Follicle Activation During Transplantation of Cryopreserved Ovarian Tissue.

Authors:  Carmen Terren; Carine Munaut
Journal:  Reprod Sci       Date:  2020-09-28       Impact factor: 3.060

9.  The Effectiveness of Anti-Apoptotic Agents to Preserve Primordial Follicles and Prevent Tissue Damage during Ovarian Tissue Cryopreservation and Xenotransplantation.

Authors:  Sanghoon Lee; Hyun-Woong Cho; Boram Kim; Jae Kwan Lee; Tak Kim
Journal:  Int J Mol Sci       Date:  2021-03-03       Impact factor: 5.923

10.  Hydrostatic pressure improves in-vitro maturation of oocytes derived from vitrified-warmed mouse ovaries.

Authors:  Zahra Rashidi; Mehri Azadbakht; Mozafar Khazaei
Journal:  Iran J Reprod Med       Date:  2012-05
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.