5.1 cells. In addition, the exosome-mediated miR-199* transfer markedly attenuated the expression of HCV replicon RNA via targeting a binding site located at HCV 5′-UTR. Conclusions: Our results demonstrated that AMSC-derived exosomes can be used as a vehicle for delivery of anti-HCV miRNAs and that exosomes-me-diated miR-199* Tipifarnib deliver may represent a new strategy against HCV. Disclosures: The following people have nothing to disclose: Guohua Lou, Yanning Liu, Zhi Chen Background:
siRNA is positioned to be a promising therapeutic drug. However, the drug delivery system of siRNA to the appropriate tissue remains a major problem for clinical application. Nek2 (NIMA-related kinase 2) is a member of the serine/thre-onine kinase family, which is related to the essential mitotic regulator NIMA. We reported the efficiency of Nek2 siRNA in several cancer xenograft models using cholangiocarcinoma, breast cancer, and colorectal cancer cell lines. However, the efficacy of Nek2 siRNA for the liver metastasis has never been demonstrated. Purpose: To evaluate
the efficiency of portal venous port-catheter system as an administrative route of siRNA to the liver metastasis. Methods: A liver metastasis xenograft model was established by injecting pancreatic cancer cells via the ileocolic vein. Thereafter, the venous port-catheter was inserted to the portal vein via the splenic vein. A port chamber was embedded under the skin for repeating injection of Nek2 siRNA. Nek2 siRNA/liposome complexes were formed with Nek2 siRNA (50μM, 100μl) and liposome (100μl), and were administered 5 times per week. Palbociclib Control group was treated with Control siRNA (non-silencing siRNA) /liposome complexes. The total number and total volume of liver metastasis was analyzed. The cellular uptakes of fluorescence labeled Nek2 siRNA/liposome complexes were evaluated in the liver metastasis by intravital microscopy. Results and Discussion: In the liver metastasis model, the
total number and volume of Bcl-w metastasis were lower in the group with Nek2 siRNA treatment compared to the group with Control siRNA treatment. There was no complication related to the portal venous port-catheter system. Intravital microscopic analysis revealed that the fluorescence labeled Nek2 siRNA/liposome complexes were localized in the hepatocytes around the portal triad 1 h after the siRNA administration. The venous port-catheter system has applied to the clinic. Anticancer drugs are able to administer directly into the tumor. The portal venous port-catheter system is less invasive than surgical operation without adverse side effects. Nek2 siRNA administration using this procedure efficiently prevented the progression of liver metastasis. Our results showed that this procedure is effective as the drug delivery system of siRNA for liver metastasis.