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Development of a hammerhead ribozyme against bcl‐2. I. Preliminary evaluation of a potential gene therapeutic agent for hormone‐refractory human prostate cancer
Author(s) -
Dorai Thambi,
Olsson Carl A.,
Katz Aaron E.,
Buttyan Ralph
Publication year - 1997
Publication title -
the prostate
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.295
H-Index - 123
eISSN - 1097-0045
pISSN - 0270-4137
DOI - 10.1002/(sici)1097-0045(19970901)32:4<246::aid-pros4>3.0.co;2-h
Subject(s) - lncap , ribozyme , biology , hammerhead ribozyme , cancer research , transfection , prostate cancer , rna , messenger rna , cancer cell , genetic enhancement , microbiology and biotechnology , gene , cancer , biochemistry , genetics
BACKGROUND The bcl‐2 oncoprotein suppresses apoptosis and, when overexpressed in prostate cancer cells, makes these cells resistant to a variety of therapeutic agents, including hormonal ablation. Therefore, bcl‐2 provides a strategic target for the development of gene knockout therapies to treat human prostate cancers. Towards this end, we have synthesized an anti‐bcl‐2 gene therapeutic reagent based on ribozyme technology and have tested its effectiveness against bcl‐2 mRNA in vitro and in vivo. METHODS A divalent hammerhead ribozyme was constructed by recombining two catalytic RNA domains into an antisense segment of the coding region for human bcl‐2 mRNA. A disabled ribozyme lacking catalytic activity was also constructed as a control reagent for our experiments. The ribozymes were tested for endonucleolytic activity against synthetic and natural bcl‐2 mRNAs. Simple transfection procedures were then utilized to introduce the ribozymes into cultured prostate cancer cells (LNCaP derivatives). We measured the effects of the ribozymes on endogenous expression of bcl‐2 mRNA and protein in these cells as well as their ability to induce apoptosis. RESULTS The functional but not the disabled ribozyme was able to rapidly degrade bcl‐2 mRNA in vitro, without the requirement for any other cellular protein or factor. When directly transfected into LNCaP cell variants, it significantly reduced bcl‐2 mRNA and protein levels within 18 hr of treatment. This activity was sufficient to induce apoptosis in a low‐bcl‐2‐expressing variant of LNCaP, but not in a high‐bcl‐2‐expressing LNCaP line. For the high‐bcl‐2‐expressing variant, however, it did restore the ability to genetically respond to a secondary apoptotic agent, phorbol ester, as evidenced by the renewed ability of phorbol ester to induce NGF1A mRNA in these cells. CONCLUSIONS This study supports the potential utility of an anti‐bcl‐2 ribozyme reagent for reducing or eliminating bcl‐2 expression from hormone‐refractory prostate cancer cells and for killing prostate cancer cells. As such, it is the first step toward an effective gene therapy against hormone‐refractory human prostate cancers. Prostate 32:246–258, 1997. © 1997 Wiley‐Liss, Inc.