Custirsen (OGX-011): Clusterin Inhibitor in Metastatic Prostate Cancer

被引:13
作者
Al-Asaaed, Sohaib [1 ]
Winquist, Eric [1 ,2 ]
机构
[1] Univ Western Ontario, Dept Oncol, Div Med Oncol, London, ON, Canada
[2] London Hlth Sci Ctr, London, ON N6A 4L6, Canada
关键词
Custirsen; Clusterin; Prostate cancer; Antisense oligonucleotides; Resistance; ENHANCE ANDROGEN-SENSITIVITY; MITOXANTRONE PLUS PREDNISONE; RANDOMIZED PHASE-II; ANTISENSE OLIGONUCLEOTIDE; ANTIAPOPTOTIC GENE; MOLECULAR-MECHANISMS; TARGETING CLUSTERIN; INCREASED SURVIVAL; PROTEIN CLUSTERIN; MORTALITY-RATES;
D O I
10.1007/s11912-012-0285-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:113 / 118
页数:6
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