Retrievable hydrogels for ovarian follicle transplantation and oocyte collection.
Peter D RiosEkaterina KniazevaHoi Chang LeeShuo XiaoRobert S OakesEiji SaitoJacqueline S JerussAriella ShikanovTeresa K WoodruffLonnie D SheaPublished in: Biotechnology and bioengineering (2018)
Cancer survivorship rates have drastically increased due to improved efficacy of oncologic treatments. Consequently, clinical concerns have shifted from solely focusing on survival to quality of life, with fertility preservation as an important consideration. Among fertility preservation strategies for female patients, ovarian tissue cryopreservation and subsequent reimplantation has been the only clinical option available to cancer survivors with cryopreserved tissue. However, follicle atresia after transplantation and risk of reintroducing malignant cells have prevented this procedure from becoming widely adopted in clinics. Herein, we investigated the encapsulation of ovarian follicles in alginate hydrogels that isolate the graft from the host, yet allows for maturation after transplantation at a heterotopic (i.e., subcutaneous) site, a process we termed in vivo follicle maturation. Survival of multiple follicle populations was confirmed via histology, with the notable development of the antral follicles. Collected oocytes (63%) exhibited polar body extrusion and were fertilized by intracytoplasmic sperm injection and standard in vitro fertilization procedures. Successfully fertilized oocytes developed to the pronucleus (14%), two-cell (36%), and four-cell (7%) stages. Furthermore, ovarian follicles cotransplanted with metastatic breast cancer cells within the hydrogels allowed for retrieval of the follicles, and no mice developed tumors after removal of the implant, confirming that the hydrogel prevented seeding of disease within the host. Collectively, these findings demonstrate a viable option for safe use of potentially cancer-laden ovarian donor tissue for in vivo follicle maturation within a retrievable hydrogel and subsequent oocyte collection. Ultimately, this technology may provide novel options to preserve fertility for young female patients with cancer.
Keyphrases
- childhood cancer
- drug delivery
- hyaluronic acid
- tissue engineering
- cell therapy
- wound healing
- papillary thyroid
- young adults
- single cell
- end stage renal disease
- breast cancer cells
- ejection fraction
- primary care
- chronic kidney disease
- induced apoptosis
- small cell lung cancer
- type diabetes
- prognostic factors
- minimally invasive
- newly diagnosed
- oxidative stress
- mesenchymal stem cells
- cell proliferation
- lymph node metastasis
- pulmonary embolism
- metabolic syndrome
- robot assisted
- ionic liquid
- peritoneal dialysis
- free survival
- soft tissue
- pi k akt
- high resolution
- single molecule
- patient reported