Abstract
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.
Footnotes
Work at the University College of London School of Pharmacy was supported by Cancer Research UK Program to S.N. [Grant C129/A4489]. S.M.H. was funded by the Philipp Brown Trust. Work at the German Cancer Research Center was funded by grants from the Deutsche Krebshilfe–Tumorstammzellverbund, and the BMBF (Bundesministerium für Forschung und Technik) UV-A Konsortium (both to P.B.). This research was supported by National Institutes of Health National Cancer Institute [Grant HHSN261200800001E.] The content of this publication does not necessarily reflect the views or policies of the Department of Health and Human Services, nor does mention of trade names, commercial products, or organizations imply endorsement by the US Government.
↵This article has supplemental material available at molpharm.aspetjournals.org.
- Received July 8, 2012.
- Accepted November 27, 2012.
- Copyright © 2013 by The American Society for Pharmacology and Experimental Therapeutics
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