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RNA Interference–Mediated Silencing of the Acetyl-CoA-Carboxylase- Gene Induces Growth Inhibition and Apoptosis of Prostate Cancer Cells

Laboratory for Experimental Medicine and Endocrinology, University of Leuven, Leuven, Belgium

Requests for reprints: Johannes V. Swinnen, Laboratory for Experimental Medicine and Endocrinology, Gasthuisberg, O&N niv 9, Herestraat 49, bus 902, B-3000, Leuven, Belgium. Phone: 32-16-345974; Fax: 32-16-345934; E-mail: johan.swinnen{at}med.kuleuven.be.

Overexpression of lipogenic enzymes is a common characteristic of many cancers. Thus far, studies aimed at the exploration of lipogenic enzymes as targets for cancer intervention have focused on fatty acid synthase (FAS), the enzyme catalyzing the terminal steps in fatty acid synthesis. Chemical inhibition or RNA interference (RNAi)–mediated knockdown of FAS consistently inhibits the growth and induces death of cancer cells. Accumulation of the FAS substrate malonyl-CoA has been implicated in the mechanism of cytotoxicity of FAS inhibition. Here, using RNAi technology, we have knocked down the expression of acetyl-CoA carboxylase- (ACC-), the enzyme providing the malonyl-CoA substrate. Silencing of the ACC- gene resulted in a similar inhibition of cell proliferation and induction of caspase-mediated apoptosis of highly lipogenic LNCaP prostate cancer cells as observed after FAS RNAi. In nonmalignant cells with low lipogenic activity, no cytotoxic effects of knockdown of ACC- or FAS were observed. These findings indicate that accumulation of malonyl-CoA is not a prerequisite for cytotoxicity induced by inhibition of tumor-associated lipogenesis and suggest that in addition to FAS, ACC- is a potential target for cancer intervention.

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