Reappraisal of glucocorticoids in castrate-resistant prostate cancer
- PMID: 24994787
- PMCID: PMC4215665
- DOI: 10.4103/1008-682X.133314
Reappraisal of glucocorticoids in castrate-resistant prostate cancer
Abstract
Recent reports and discussions of preclinical prostate cancer models have emphasized the possibility that enzalutamide resistance may be mediated by glucocorticoid receptors (GR). In both in vitroand xenograft animal studies, it is possible to show that the GR is up-regulated in prostate cancer cell lines and that dexamethasone reverses enzalutamide induced growth inhibition. In these model systems, GR agonists can induce a subset of androgen receptor target genes including prostate-specific antigen. These investigators also report a correlation between GR expression in patient-derived prostate cancer specimens and clinical response to enzalutamide. The authors discuss the possibility that these findings have important clinical relevance. We note that the current clinical evidence for GR mediating drug resistance or disease progression in patients with castrate-resistant prostate cancer (CRPC) is very limited at best.
Comment on
-
Glucocorticoid receptor confers resistance to antiandrogens by bypassing androgen receptor blockade.Cell. 2013 Dec 5;155(6):1309-22. doi: 10.1016/j.cell.2013.11.012. Cell. 2013. PMID: 24315100 Free PMC article.
-
Steroid receptors aplenty in prostate cancer.N Engl J Med. 2014 Mar 6;370(10):970-1. doi: 10.1056/NEJMcibr1315706. N Engl J Med. 2014. PMID: 24597872 No abstract available.
References
-
- Sharifi N. Steroid receptors aplenty in prostate cancer. N Engl J Med. 2014;370:970–1. - PubMed
-
- Scher HI, Zhang ZF, Nanus D, Kelly WK. Hormone and antihormone withdrawal: implications for the management of androgen-independent prostate cancer. Urology. 1996;47:61–9. - PubMed
-
- Taplin ME, Manola J, Oh WK, Kantoff PW, Bubley GJ, et al. A phase II study of mifepristone (RU-486) in castration-resistant prostate cancer, with a correlative assessment of androgen-related hormones. BJU Int. 2008;101:1084–9. - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical