New steroidal 17I2-carboxy derivatives present anti-5I--reductase activity and anti-proliferative effects in a human androgen-responsive prostate cancer cell line

• Published in: Biochimie 2013-11, Vol.95 (11), p.2097-2106
• Main Authors: Amaral, Cristina, Varela, Carla, Correia-da-Silva, Georgina, Silva, ElisiA!rio, Carvalho, Rui, Costa, Saul, Cunha, Sara, Fernandes, Jose, Teixeira, Natercia, Roleira, Fernanda
• Format: Article
• Language: English
• ISSN: 0300-9084
• DOI: 10.1016/j.biochi.2013.07.023

The androgens testosterone (T) and dihydrotestosterone (DHT), besides playing an important role in prostate development and growth, are also responsible for the development and progression of benign prostate hyperplasia (BPH) and prostate cancer. Therefore, the actions of these hormones can be antagonized by preventing the irreversible conversion of T into DHT by inhibiting 5I--reductase (5I--R). This has been a useful therapeutic approach for the referred diseases and can be achieved by using 5I--reductase inhibitors (RIs). Steroidal RIs, finasteride and dutasteride, are used in clinic for BPH treatment and were also proposed for chemoprevention of prostate cancer. Nevertheless, due to the increase in bone and muscle loss, impotency and occurrence of high-grade prostate tumours, it is important to seek for other potent and specific molecules with lower side effects. In the present work, we designed and synthesized steroids with the 3-keto-I4 moiety in the A-ring, as in the 5I--R substrate T, and with carboxamide, carboxyester or carboxylic acid functions at the C-17I2 position. The inhibitory 5I--R activity, in human prostate microsomes, as well as the anti-proliferative effects of the most potent compounds, in a human androgen-responsive prostate cancer cell line (LNCaP cells), were investigated. Our results showed that steroids 3, 4 and 5 are good RIs, which suggest that C-17I2 lipophylic amides favour 5I--R inhibition. Moreover, these steroids induce a decrease in cell viability of stimulated LNCaP cells, in a 5I--R dependent-manner, similarly to finasteride.