Atu027, a Liposomal Small Interfering RNA Formulation Targeting Protein Kinase N3, Inhibits Cancer Progression

被引:235
作者
Aleku, Manuela
Schulz, Petra [1 ]
Keil, Oliver
Santel, Ansgar
Schaeper, Ute
Dieckhoff, Britta
Janke, Oliver
Endruschat, Jens
Durieux, Birgit
Roeder, Nadine
Loeffler, Kathrin
Lange, Christian
Fechtner, Melanie
Moepert, Kristin
Fisch, Gerald
Dames, Sibylle
Arnold, Wolfgang
Jochims, Karin [3 ]
Giese, Klaus
Wiedenmann, Bertram [1 ]
Scholz, Arne [1 ]
Kaufmann, Joerg [2 ]
机构
[1] Charite, Med Klin Schwerpunkt Hepatol & Gastroenterol, D-13353 Berlin, Germany
[2] Silence Therapeut AG, Otto Warburg Haus, D-13125 Berlin, Germany
[3] IASON Consulting, Niederzier, Germany
关键词
D O I
10.1158/0008-5472.CAN-08-2428
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We have previously described a small interfering RNA (siRNA) delivery system (AtuPLEX) for RNA interference (RNAi) in the vasculature of mice. Here we report preclinical data for Atu027, a siRNA-lipoplex directed against protein kinase N3 (PKN3), currently under development for the treatment of advanced solid cancer. In vitro studies revealed that Atu027-mediated inhibition of PKN3 function in primary endothelial cells impaired tube formation on extracellular matrix and cell migration, but is not essential for proliferation. Systemic administration of Atu027 by repeated bolus injections or infusions in mice, rats, and nonhuman primates results in specific, RNAi-mediated silencing of PKN3 expression. We show the efficacy of Atu027 in orthotopic mouse models for prostate and pancreatic cancers with significant inhibition of tumor growth and lymph node metastasis formation. The tumor vasculature of Atu027-treated animals showed a specific reduction in lymph vessel density but no significant changes in microvascular density. [Cancer Res 2008;68(23):9788-98]
引用
收藏
页码:9788 / 9798
页数:11
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