On the Road to Fight Cancer: The Potential of G-Quadruplex Ligands as Novel Therapeutic Agents

被引:66
作者
Alessandrini, Irene [1 ]
Recagni, Marta [1 ]
Zaffaroni, Nadia [1 ]
Folini, Marco [1 ]
机构
[1] Fdn IRCCS Ist Nazl Tumori Milano, Dept Appl Res & Technol Dev, Mol Pharmacol Unit, Via GA Amadeo 42, I-20133 Milan, Italy
关键词
anticancer therapy; cell defense mechanisms; cancer; gene promoters; G-quadruplex; synthetic lethality; telomeres; TELOMERIC G-QUADRUPLEX; RNA G-QUADRUPLEXES; C-MYC; SYNTHETIC LETHALITY; ANTIPROLIFERATIVE ACTIVITY; BINDING-PROPERTIES; DNA-DAMAGE; IN-VITRO; TARGET; STABILIZATION;
D O I
10.3390/ijms22115947
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
Nucleic acid sequences able to adopt a G-quadruplex conformation are overrepresented within the human genome. This evidence strongly suggests that these genomic regions have been evolutionary selected to play a pivotal role in several aspects of cell biology. In the present review article, we provide an overview on the biological impact of targeting G-quadruplexes in cancer. A variety of small molecules showing good G-quadruplex stabilizing properties has been reported to exert an antitumor activity in several preclinical models of human cancers. Moreover, promiscuous binders and multiple targeting G-quadruplex ligands, cancer cell defense responses and synthetic lethal interactions of G-quadruplex targeting have been also highlighted. Overall, evidence gathered thus far indicates that targeting G-quadruplex may represent an innovative and fascinating therapeutic approach for cancer. The continued methodological improvements, the development of specific tools and a careful consideration of the experimental settings in living systems will be useful to deepen our knowledge of G-quadruplex biology in cancer, to better define their role as therapeutic targets and to help design and develop novel and reliable G-quadruplex-based anticancer strategies.
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页数:23
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