School of Pharmacy, University College London, London, United Kingdom.
Mol Pharmacol. 2013 Feb;83(2):470-80. doi: 10.1124/mol.112.081075. Epub 2012 Nov 27.
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.
四聚体是一种高级核酸结构,可以在富含 G 的端粒和致癌基因的启动子区域形成。小分子稳定四聚体可以导致端粒去帽,随后引发 DNA 损伤反应和衰老,以及染色体融合导致有丝分裂失控,随后凋亡和下调致癌基因表达。我们在这里根据细胞生物学数据以及国家癌症研究所 COMPARE 研究报告了对四取代萘二酰亚胺配体作用机制的研究。我们得出结论,这些化合物涉及四种主要作用机制:1)端粒去帽,随后引发 DNA 损伤反应和衰老;2)抑制致癌基因的转录/翻译;3)通过端粒 DNA 末端融合导致基因组不稳定,导致有丝分裂灾难和凋亡;4)通过端粒聚集形成诱导染色体不稳定。