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Cancer Research 66, 10534, November 1, 2006. doi: 10.1158/0008-5472.CAN-06-2393
© 2006 American Association for Cancer Research

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Experimental Therapeutics, Molecular Targets, and Chemical Biology

Targeting Cancer Cells by Novel Engineered Modular Transporters

Dinara G. Gilyazova1,2, Andrey A. Rosenkranz1,2, Pavel V. Gulak1, Vladimir G. Lunin1,3, Olga V. Sergienko3, Yuri V. Khramtsov1, Kirill N. Timofeyev2, Mikhail A. Grin4, Andrey F. Mironov4, Andrey B. Rubin2, Georgii P. Georgiev1 and Alexander S. Sobolev1,2

1 Institute of Gene Biology, Russian Academy of Sciences; 2 Biological Faculty, Moscow State University; 3 Gamaleya Institute of Epidemiology and Microbiology, Russian Academy of Medical Sciences; and 4 Moscow State Academy of Fine Chemical Technology, Moscow, Russia

Requests for reprints: Alexander S. Sobolev, Department of Molecular Genetics of Intracellular Transport, Institute of Gene Biology, Russian Academy of Sciences, 34/5 Vavilov Street, 119334, Moscow, Russia. Phone: 7-495-135-3100; Fax: 7-495-135-4105; E-mail: sobolev{at}igb.ac.ru.

A major problem in the treatment of cancer is the specific targeting of drugs to these abnormal cells. Ideally, such a drug should act over short distances to minimize damage to healthy cells and target subcellular compartments that have the highest sensitivity to the drug. We describe the novel approach of using modular recombinant transporters to target photosensitizers to the nucleus, where their action is most pronounced, of cancer cells overexpressing ErbB1 receptors. We have produced a new generation of the transporters consisting of (a) epidermal growth factor as the internalizable ligand module to ErbB1 receptors, (b) the optimized nuclear localization sequence of SV40 large T-antigen, (c) a translocation domain of diphtheria toxin as an endosomolytic module, and (d) the Escherichia coli hemoglobin-like protein HMP as a carrier module. The modules retained their functions within the transporter chimera: they showed high-affinity interactions with ErbB1 receptors and {alpha}/ß-importin dimers and formed holes in lipid bilayers at endosomal pH. A photosensitizer conjugated with the transporter produced singlet oxygen and ·OH radicals similar to the free photosensitizer. Photosensitizers-transporter conjugates have >3,000 times greater efficacy than free photosensitizers for target cells and were not photocytotoxic at these concentrations for cells expressing a few ErbB1 receptors per cell, in contrast to free photosensitizers. The different modules of the transporters, which are highly expressed and easily purified to retain full activity of each of the modules, are interchangeable, meaning that they can be tailored for particular applications. (Cancer Res 2006; 66(21): 10534-40)







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 2006 by the American Association for Cancer Research.