the hdac inhibitor fk228 enhances adenoviral transgene expression by a transduction-independent mechanism but does not increase adenovirus replicationhdac抑制剂fk228提高adenoviral transduction-independent转基因表达的机制,但并不增加腺病毒复制.pdfVIP

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2017-09-12 发布于上海
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the hdac inhibitor fk228 enhances adenoviral transgene expression by a transduction-independent mechanism but does not increase adenovirus replicationhdac抑制剂fk228提高adenoviral transduction-independent转基因表达的机制,但并不增加腺病毒复制.pdf

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the hdac inhibitor fk228 enhances adenoviral transgene expression by a transduction-independent mechanism but does not increase adenovirus replicationhdac抑制剂fk228提高adenoviral transduction-independent转基因表达的机制,但并不增加腺病毒复制

The HDAC Inhibitor FK228 Enhances Adenoviral Transgene Expression by a Transduction-Independent Mechanism but Does Not Increase Adenovirus Replication Angelika Danielsson*, Helena Dzojic, Victoria Rashkova, Wing-Shing Cheng, Magnus Essand Department of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, Uppsala, Sweden Abstract The histone deacetylase inhibitor FK228 has previously been shown to enhance adenoviral transgene expression when cells are pre-incubated with the drug. Upregulation of the coxsackie adenovirus receptor (CAR), leading to increased viral transduction, has been proposed as the main mechanism. In the present study, we found that the highest increase in transgene expression was achieved when non-toxic concentrations of FK228 were added immediately after transduction, demonstrating that the main effect by which FK228 enhances transgene expression is transduction-independent. FK228 had positive effects both on Ad5 and Ad5/f35 vectors with a variety of transgenes and promoters, indicating that FK228 works mainly by increasing transgene expression at the transcriptional level. In some cases, the effects were dramatic, as demonstrated by an increase in CD40L expression by FK228 from 0.3% to 62% when the murine prostate cancer cell line TRAMP-C2 was transduced with Ad[CD40L]. One unexpected finding was that FK228 decreased the transgene expression of an adenoviral vector with the prostate cell-specific PPT promoter in the human prostate adenocarcinoma cell lines LNCaP and PC-346C. This is probably a consequence of alteration of the adenocarcinoma cell lines towards a neuroendocrine differentiation after FK228 treatment. The observations in this study indicate that FK228 enhances adenoviral therapy by a transduction-independent mechanism. Furthermore, s