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Stimuli-sensitive combination nano-preparations of si-RNA and chemotherapeutic drugs to treat multidrug resistant cancers
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Cancer Science & Therapy

ISSN: 1948-5956

Open Access

Stimuli-sensitive combination nano-preparations of si-RNA and chemotherapeutic drugs to treat multidrug resistant cancers


8th Euro Global Summit on Cancer Therapy

November 03-05, 2015 Valencia, Spain

Vladimir Torchilin

Northeastern University, USA

Keynote: J Cancer Sci Ther

Abstract :

Tumor therapy, especially in the case of multidrug resistant cancers, could be significantly enhanced by using si-RNA downregulating the production of proteins, which are involved in cancer cell resistance, such as Pgp or survivin. Even better response could be achieved is such si-RNA could be delivered to tumors together with chemotherapeutic agent. This task is complicated by low stability of si-RNA in biological surrounding. Thus, the delivery system should simultaneously protect si-RNA from degradation. We have developed several types of lipid-core polymeric micelles based on PEG-phospholipid or PEI-phospholipid conjugates, which are biologically inert, demonstrate prolonged circulation in the blood and can firmly bind non-modified or reversibly-modified si-RNA. Additionally, these nano-preparations can be loaded into their lipidic core with poor water soluble chemotherapeutic agents, such as paclitaxel or camptothecin. In experiments with cancer cell monolayers, cancer cell 3D spheroids, and in animals with implanted tumors, it was shown that such co-loaded preparations can significantly down-regulate target proteins in cancer cells, enhance drug activity, and reverse multidrug resistance. In order to specifically unload such nano-preparations inside tumors, those can be designed sensitive to local tumor-specific stimuli, such as lowered pH, hypoxia, or overexpressed certain enzymes, such as matrix metallo-proteases. Using pH-, hypoxia-, or MMP2-sensitive bonds between different components of nano-preparations co-loaded with si-RNA and drugs, one can be able to make the systems specifically delivering biologically active agents in tumors, inside tumor cells, or even to individual cell organelles, which resulted in significantly improved therapeutic response.

Biography :

Vladimir Torchilin is University Distinguished Professor and Director, Center for Pharmaceutical Biotechnology and Nano-medicine, Northeastern University, Boston. He has published more than 350 original papers, more than 150 reviews and book chapters, wrote and edited 10 books and holds more than 40 patents. He is Editor-in-Chief of Current Drug Discovery Technologies and of Drug Delivery. He is a Member of European Academy of Sciences, Fellow of AIMBE, AAPS and CRS, and received many important national and international awards including the 2013 Blaise Pascal Medal in Biomedicine from EAS. In 2005, he was a President of the CRS and in 2011 Times Higher Education ranked him number 2 among top world scientists in pharmacology for 2001-2010.

Email: v.torchilin@neu.ed

Google Scholar citation report
Citations: 3968

Cancer Science & Therapy received 3968 citations as per Google Scholar report

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