Volume 16, Issue 1 (January 2014) 16, 99–100; 10.4103/1008-682X.122200
More evidence intratumoral DHT synthesis drives castration-resistant prostate cancer
Elizabeth M. Wilson
Laboratories for Reproductive Biology, Department of Pediatrics, Lineberger Comprehensive Cancer Center, Department of Biochemistry and Biophysics, University of North Carolina, Chapel Hill, NC, USA
Correspondence: Wilson Elizabeth M
2013-12-16
Abstract |
A gain-of-function stabilizing somatic mutation in 3β-hydroxysteroid dehydrogenase type 1 (3βHSD1, HSD3B1) was reported in castration-resistant prostate cancer. The A→C nucleotide polymorphism replaced asparagine-367 with threonine (3βHSD1-N367T) as a homozygous somatic mutation in a subset of castration-resistant prostate cancers by loss of heterozygosity of the wild-type allele. Increased stability of 3βHSD1-N367T was associated with decreased ubiquitin-mediated degradation and higher levels of dihydrotestosterone (DHT). The studies suggest that genetic instability in castration-resistant prostate cancer favors the more stable 3βHSD1-N367T mutant that contributes to drug resistance. A somatic mutation in a steroid metabolic enzyme required for DHT synthesis provides further support for intratumoral androgen synthesis contributing to prostate cancer progression.
Full Text |
PDF |
PDF |
|
|
Browse: 2465 |
|