Inhibitors of N-glycosylation as a potential tool for analysis of the mechanism of action and cellular localisation of glycoprotein P.
Author(s) -
Karolina Wojtowicz,
Witold Szaflarski,
Radosław Januchowski,
Piotr Zawierucha,
Michał Nowicki,
M. Zabel
Publication year - 2012
Publication title -
acta biochimica polonica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.452
H-Index - 78
eISSN - 1734-154X
pISSN - 0001-527X
DOI - 10.18388/abp.2012_2076
Subject(s) - glycosylation , glycoprotein , multiple drug resistance , p glycoprotein , mechanism of action , intracellular , mechanism (biology) , chemistry , n linked glycosylation , membrane glycoproteins , biochemistry , microbiology and biotechnology , biology , glycan , in vitro , antibiotics , philosophy , epistemology
Multidrug resistance has for many years attracted attention of numerous investigators. Attempts have also been made to increase efficiency of anti-neoplastic therapy. For this reason, most of efforts have been devoted to analysing proteins engaged in the mechanism of multidrug resistance such as the N-glycosylated membrane protein glycoprotein P. Interestingly, glycosylation probably plays a significant role in the intracellular location and activity of modified proteins. Inhibitors of glycosylation have been demonstrated to alter the activity of glycoprotein P in various ways, depending on the cell line examined. These inhibitors markedly reduce multidrug resistance of cancer cells, thus promoting success of anti-neoplastic therapy. Here, we review the basic knowledge on N-glycosylation inhibitors, their effect on glycoprotein P and their therapeutic potential.
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