Suppression of activin-induced apoptosis by novel antisense strategy in human prostate cancer cells

被引:4
作者
Ying, SY
Chuong, CM
Lin, SL
机构
[1] Univ So Calif, Dept Cell & Neurobiol, Sch Med, Los Angeles, CA 90033 USA
[2] Univ So Calif, Dept Pathol, Sch Med, Los Angeles, CA 90033 USA
[3] Epiclone Inc, Alhambra, CA 91801 USA
关键词
activin; covalent-binding antisense probes; apoptosis; gene knockout; prostate cancer;
D O I
10.1006/bbrc.1999.1742
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
Apoptosin, a novel gene encoding a mitotic kinase-motif protein, is stimulated by activin, a member of TGF-beta family, in human LNCaP prostate cancer cells and in patient tissues. We employed a gene knockout methodology based on the covalent bonding of chemically modified antisense probes to apoptosin mRNAs in LNCaP cells. The mRNA-antisense hybrid duplexes were neither translated nor post-transcriptionally modified, resulting in no protein synthesis, Introducing antisense apoptosin into activin-induced apoptotic LNCaP cells prevented apoptosis, interfered with genomic DNA fragmentation and released cell cycle checkpoint. These findings suggest that the apoptosin, in addition to p53, is important in apoptotic regulation of human prostate cancers. (C) 1999 Academic Press.
引用
收藏
页码:669 / 673
页数:5
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