Polymer Carriers for Anticancer Drugs Targeted to EGF Receptor

被引:15
|
作者
Studenovsky, Martin [1 ]
Pola, Robert [1 ]
Pechar, Michal [1 ]
Etrych, Tomas [1 ]
Ulbrich, Karel [1 ]
Kovar, Lubomir [2 ]
Kabesova, Martina [2 ]
Rihova, Blanka [2 ]
机构
[1] Acad Sci Czech Republ, Inst Macromol Chem, CR-16206 Prague 6, Czech Republic
[2] Acad Sci Czech Republ, Inst Microbiol, CR-14220 Prague 4, Czech Republic
关键词
biocompatibility; EGFR; peptides; polymer conjugates; tumor drug delivery; GROWTH-FACTOR RECEPTOR; MACROMOLECULAR THERAPEUTICS; IN-VIVO; CANCER; ACCUMULATION; EXPRESSION; COPOLYMERS; PROTEINS; LINES;
D O I
10.1002/mabi.201200270
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A novel actively targeted polymer carrier for anticancer drugs based on an N-(2-hydroxypropyl)methacrylamide copolymer (PHPMA) is proposed. An oligopeptide sequence GE7, attached to the polymer, is a specific ligand for the EGF receptor overexpressed on most tumor cells. Co-attachment of selected chemotherapeutics will therefore lead to formation of tumor-specific polymer therapeutics, further enhanced by the EPR effect. FACS measurements prove elevated binding activity of the fluorescently labeled PHPMA/GE7 conjugate in EGFR-rich cells (FaDu, MCF-7), compared to conjugates of scrambled peptides. Cell lines with low EGFR level (SW620, B16F10) bind the GE7 conjugate significantly less.
引用
收藏
页码:1714 / 1720
页数:7
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