| Literature DB >> 27356095 |
Eva De Mol1, R Bryn Fenwick1, Christopher T W Phang1, Victor Buzón2, Elzbieta Szulc1, Alex de la Fuente1, Albert Escobedo1, Jesús García1, Carlos W Bertoncini1, Eva Estébanez-Perpiñá2, Iain J McEwan3, Antoni Riera1,4, Xavier Salvatella1,5.
Abstract
Castration-resistant prostate cancer is the lethal condition suffered by prostate cancer patients that become refractory to androgen deprivation therapy. EPI-001 is a recently identified compound active against this condition that modulates the activity of the androgen receptor, a nuclear receptor that is essential for disease progression. The mechanism by which this compound exerts its inhibitory activity is however not yet fully understood. Here we show, by using high resolution solution nuclear magnetic resonance spectroscopy, that EPI-001 selectively interacts with a partially folded region of the transactivation domain of the androgen receptor, known as transactivation unit 5, that is key for the ability of prostate cells to proliferate in the absence of androgens, a distinctive feature of castration-resistant prostate cancer. Our results can contribute to the development of more potent and less toxic novel androgen receptor antagonists for treating this disease.Entities:
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Year: 2016 PMID: 27356095 PMCID: PMC5027137 DOI: 10.1021/acschembio.6b00182
Source DB: PubMed Journal: ACS Chem Biol ISSN: 1554-8929 Impact factor: 5.100