Mechanism of the Antiproliferative Activity of Some Naphthalene Diimide G-Quadruplex Ligands

被引:27
|
作者
Hampel, Sonja M. [1 ]
Pepe, Antonella [2 ]
Greulich-Bode, Karin M. [3 ]
Malhotra, Sanjay V. [2 ]
Reszka, Anthony P. [1 ]
Veith, Sebastian [4 ]
Boukamp, Petra [3 ]
Neidle, Stephen [1 ]
机构
[1] UCL, Sch Pharm, London WC1N 1AX, England
[2] SAIC Frederick Inc, Lab Synthet Chem, Dev Therapeut Program Support, Frederick Natl Lab Canc Res, Frederick, MD USA
[3] German Canc Res Ctr, Heidelberg, Germany
[4] Univ Konstanz, Mol Toxicol Grp, Dept Biol, Constance, Germany
基金
美国国家卫生研究院;
关键词
TELOMERIC G-QUADRUPLEXES; DNA-DAMAGE RESPONSE; CHROMOSOMAL REARRANGEMENTS; SMALL-MOLECULE; CANCER; ATM; APOPTOSIS; BINDING; TRF2; STABILIZATION;
D O I
10.1124/mol.112.081075
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
G-quadruplexes are higher-order nucleic acid structures that can form in G-rich telomeres and promoter regions of oncogenes. Telomeric quadruplex stabilization by small molecules can lead to telomere uncapping, followed by DNA damage response and senescence, as well as chromosomal fusions leading to deregulation of mitosis, followed by apoptosis and downregulation of oncogene expression. We report here on investigations into the mechanism of action of tetra-substituted naphthalene diimide ligands on the basis of cell biologic data together with a National Cancer Institute COMPARE study. We conclude that four principal mechanisms of action are implicated for these compounds: 1) telomere uncapping with subsequent DNA damage response and senescence; 2) inhibition of transcription/translation of oncogenes; 3) genomic instability through telomeric DNA end fusions, resulting in mitotic catastrophe and apoptosis; and 4) induction of chromosomal instability by telomere aggregate formation.
引用
收藏
页码:470 / 480
页数:11
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