Human telomeric G-quadruplex: The current status of telomeric G-quadruplexes as therapeutic targets in human cancer

被引:469
作者
Neidle, Stephen [1 ]
机构
[1] Univ London, Sch Pharm, Canc Res UK Biomol Struct Grp, London WC1N 1AX, England
关键词
acridine; anticancer; drug; drug-like; in vivo; medicinal chemistry; pharmacology; quadruplex; telomerase; telomere; DNA-DAMAGE RESPONSE; INHIBITS TUMOR-GROWTH; IN-VITRO; SMALL-MOLECULE; LIGAND RHPS4; ANTITUMOR-ACTIVITY; HUMAN-CHROMOSOMES; DRUG RECOGNITION; HUMAN GENOME; C-MYC;
D O I
10.1111/j.1742-4658.2009.07463.x
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
The 3'-ends of human chromosomal DNA terminate in short single-stranded guanine-rich tandem-repeat sequences. In cancer cells, these are associated with the telomere-maintenance enzyme telomerase together with the end-binding protein hPOT1. Small molecules that can compete with these proteins and induce the single-stranded DNA to form quadruplex-ligand complexes are, in effect, able to expose these 3'-ends, which results in the activation of a DNA damage response and selective inhibition of cell growth. Several of these G-quadruplex binding molecules have shown promising anticancer activity in tumour xenograft models, which indicate that the approach may be applicable to the treatment of a wide range of human cancers. This minireview summarizes the available data on these compounds and the challenges posed for drug discovery.
引用
收藏
页码:1118 / 1125
页数:8
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