Caspase-3 is the ultimate executioner caspase that is essential for the nuclear changes associated with apoptosis [45]. Moreover, survivin is known to directly or indirectly interact with caspase-3 and subsequently inhibit its activity. In our study, microscopic examination and scoring showed that protein expressions of bax and caspase-3 were up-regulated in P+PEI+UTMD group as compared with those of control group or P+UTMD group, while protein expressions

of survivin and bcl-2 were down-regulated markedly. The data indicated that the inhibition of survivin by administration of shRNA expression vectors with the combination of UTMD and PEI resulted in apoptosis induction in nude mice by CT99021 concentration downregulating bcl-2 expression and upregulating FK506 mw the activity of bax and caspases-3. Conclusions In summary, UTMD could synergistically promote the development and application of other gene transfer methods in vivo. It could be used as a safe and effective non-viral gene delivery system. The combination of UTMD and PEI, which could significantly enhance the gene expression of plasmid DNA in the tumor tissue, was a new method of in vivo gene transfer with a good prospect. Survivin downregulation with shRNA expression vector mediated by the UTMD and PEI technique

could obviously induce apoptosis in vivo. This method will provide a noninvasive, safe, promising candidate for tumor gene delivery. More researches are needed to further the efficient, promising novel technique for cancer gene therapy. Acknowledgements This Aurora Kinase research is supported by grant of Medical Research Foundation of Guangdong Province [No. A2010270]. References 1. Lu QL, Liang HD, Partridge T, Blomley

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