Histologic Analysis of Testes from Prepubertal Patients Treated with Chemotherapy Associates Impaired Germ Cell Counts with Cumulative Doses of Cyclophosphamide, Ifosfamide, Cytarabine, and Asparaginase.
Jose V MedranoD HervásT Vilanova-PérezA Navarro-GomezlechonE GoossensA PellicerM M AndrésE Novella-MaestrePublished in: Reproductive sciences (Thousand Oaks, Calif.) (2020)
Cryopreservation of immature testicular tissue is an experimental strategy for the preservation of fertility in prepubertal boys that will be subjected to a gonadotoxic onset, as is the case of oncologic patients. Therefore, the objective of this study was to assess the impact of chemotherapeutic treatments on the testicular histologic phenotype in prepubertal patients. A total of 56 testicular tissue samples from pediatric patients between 0 and 16 years old (28 with at least one previous chemotherapeutic onset and 28 untreated controls) were histologically analyzed and age-matched compared. At least two 5-μm sections from testis per patient separated by a distance of 100 μm were immunostained for the germ cell marker VASA, the spermatogonial markers UTF1, PLZF, UCHL1, and SALL4, the marker for proliferative cells KI67, and the Sertoli cell marker SOX9. The percentage of tubule cross-sections positive for each marker and the number of positive cells per tubule cross-section were determined and association with the cumulative dose received of each chemotherapeutic drug was statistically assessed. Results indicated that alkylating agents, cyclophosphamide and ifosfamide, but also the antimetabolite cytarabine and asparaginase were associated with a decreased percentage of positive tubules and a lower number of positive cells per tubule for the analyzed markers. Our results provide new evidences of the potential of chemotherapeutic agents previously considered to have low gonadotoxic effects such as cytarabine and asparaginase to trigger a severe testicular phenotype, hampering the potential success of future fertility restoration in experimental programs of fertility preservation in prepubertal boys.
Keyphrases
- germ cell
- induced apoptosis
- high dose
- end stage renal disease
- acute myeloid leukemia
- cell cycle arrest
- newly diagnosed
- ejection fraction
- chronic kidney disease
- low dose
- prognostic factors
- prostate cancer
- endoplasmic reticulum stress
- radiation therapy
- patient reported outcomes
- squamous cell carcinoma
- peritoneal dialysis
- signaling pathway
- cell therapy
- young adults
- minimally invasive
- patient reported
- human health
- bone marrow
- adverse drug
- peripheral blood