ABSTRACT
PURPOSE: To investigate the effects of all-trans retinoic acid (ATRA) in cisplatin (CP)-induced testicular damage in rats. MATERIALS AND METHODS: Twenty-eight male Wistar rats were divided into four groups: Control, ATRA alone, ATRA+CP, and CP alone. Body weight, testicular weight, sperm count, sperm motility, percentage of abnormal sperm, total antioxidant status (TAS), total oxidant status (TOS), oxidative stress index (OSI) in testicular tissue, and testicular histopathology were compared among groups. RESULTS: The sperm count and motility significantly decreased and the percentage of abnormal sperm significantly increased in the CP group compared to the control and ATRA groups. CP+ATRA administration significantly increased the sperm count and motility, but reduced the abnormal sperm count. CP administration significantly increased TOS and OSI compared to the control group and the other groups. Administering CP+ATRA significantly decreased TOS and the OSI in testicular tissue and reduced spermatogenesis, but increased the Johnsen score. CONCLUSIONS: The destructive effects of CP treatment on testicular tissue and spermatogenesis were reduced by administering ATRA.
Subject(s)
Animals , Humans , Male , Rats , Body Weight , Cisplatin , Oxidative Stress , Rats, Wistar , Sperm Count , Sperm Motility , Spermatogenesis , Spermatozoa , Testis , Tretinoin , Vitamin AABSTRACT
Objective: To determine the predictors of prostate cancer at repeat biopsy in patients initially diagnosed with atypical small acinar proliferation [ASAP]
Design: Retrospective study
Setting: Tepecik Training and Research Hospital, Turkey
Subjects: Among 1240 patients, only 54 patients diagnosed with ASAP on initial biopsy underwent repeat biopsy
Intervention: Patients were classified into cancer, benign and ASAP groups according to their final pathological results after repeat biopsy
Main outcome measure: The final pathological results of repeat biopsy were compared according to the clinicobiological features
Results: At the repeat 24 core prostate biopsy, the diagnoses were benign prostate, prostate cancer and ASAP in 26/54 [48.2%], 20/54 [37.03%] and 8/54 [14.8%] patients, respectively. In the cancer, ASAP and benign groups, the mean age was 67.2 +/- 5.4, 56.3 +/- 6.7 and 61.8 +/- 8.5 years, respectively. The cancer detection rate was 37.03%. Except for patient age, we found no clinical or pathological features predicting prostate cancer in patients with ASAP at repeat biopsy
Conclusion: Only the age of the patients is a predictive factor of prostate cancer at repeat biopsy in patients diagnosed with ASAP