Knock-down of the cytoprotective gene, clusterin, to enhance hormone and chemosensitivity in prostate and other cancers

被引:40
作者
Gleave, M
Chi, KN
机构
[1] Univ British Columbia, Div Urol, Vancouver Gen Hosp, Prostate Ctr, Vancouver, BC V5Z 3J5, Canada
[2] British Columbia Canc Agcy, Vancouver Canc Ctr, Vancouver, BC V5Z 4E6, Canada
来源
THERAPEUTIC OLIGONUCLEOTIDES: TRANSCRIPTIONAL AND TRANSLATIONAL STRATEGIES FOR SILENCING GENE EXPRESSION | 2005年 / 1058卷
关键词
OGX-011; prostate cancer; androgen independent; antisense oligonucleotide; Bcl-2; clusterin; TRPM-2; chemotherapy; apoptosis;
D O I
10.1196/annals.1359.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Discovery and targeting of genes mediating treatment resistance may lead to development of novel therapies that delay progression of recurrent and refractory cancers. Clusterin is a stress-associated cytoprotective chaperone expressed in many cancers that is upregulated in an adaptive cell survival manner by various apoptotic triggers and confers treatment resistance. Here, we review clusterin's functional role in regulating treatment-induced apoptosis and the use of a second generation antisense oligonucleotide to inhibit clusterin expression to enhance the cytotoxic effects of hormone- and chemotherapy in prostate and other xenograft models, as well as in recent human trials.
引用
收藏
页码:1 / 15
页数:15
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