Mechanism of acridine-based telomerase inhibition and telomere shortening

被引:120
|
作者
Gunaratnam, Mekala
Greciano, Olga
Martins, Cristina
Reszka, Anthony P.
Schultes, Christoph M.
Morjani, Hamid
Riou, Jean-Francois
Neidle, Stephen
机构
[1] Univ London, Sch Pharm, CRUK Biomol Struct Grp, London WC1N 1AX, England
[2] Univ Reims, UFR Pharm, JE 2428, Lab Onco Pharmacol, F-51096 Reims, France
关键词
G-quadruplex ligands; telomerase; telomere targeting;
D O I
10.1016/j.bcp.2007.06.011
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The trisubstituted acridine compound BRACO-19 has been developed as a ligand for stabilising G-quadruplex structures. It is shown here that BRACO-19 produces short- and long-term growth arrest in cancer cell lines, and is significantly less potent in a normal cell line. BRACO-19 reduces telomerase activity and long-term telomere length attrition is observed. It is also shown that BRACO-19 binds to telomeric single-stranded overhang DNA, consistent with quadruplex formation, and the single-stranded protein hPOT1 has been shown to be displaced from the overhang in vitro and in cellular experiments. It is concluded that the cellular activity of BRACO-19 can be ascribed both to the uncapping of 3' telomere ends and to telomere shortening that may preferentially affect cells with short telomeres. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:679 / 689
页数:11
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