Custirsen (OGX-011): clusterin inhibitor in metastatic prostate cancer
- Curr Oncol Rep. 2013 Apr;15(2):113-8. doi: 10.1007/s11912-012-0285-1.
- 1. Division of Medical Oncology, Department of Oncology, Western University, London, ON, Canada.
Adenocarcinoma of the prostate is the most common Cancer in men in the Western Hemisphere. This diagnosis includes a clinicopathologically diverse collection of disease entities, encompassing a spectrum from early localized disease to advanced-stage castration-sensitive and ultimately metastatic, castration-resistant states. Although early-stage disease is treatable and potentially curable, treatment options for castration-resistant prostate Cancer, the common pathway to prostate Cancer death, remain limited and palliative in nature. Therapeutic resistance to androgen blockade, cytotoxic chemotherapy, and radiotherapy is underpinned by a number of cellular mechanisms. The upregulation of protective, antiapoptotic chaperone proteins is one of these mechanisms, and is exemplified by the protein clusterin in castration-resistant prostate Cancer. Antisense oligonucleotide technology provides the potential to inhibit specific genes in Cancer cells and with this the possibility of a vast impact in oncology, but no antisense drugs have been approved for use in Cancer patients to date. Custirsen (OGX-011) is a novel antisense oligonucleotide drug which targets clusterin expression, and its application in prostate Cancer is reviewed in this article.