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结构视角下的 G-四链体:迈向新型抗癌药物。

Structural insights into G-quadruplexes: towards new anticancer drugs.

机构信息

College of Pharmacy, The University of Arizona, 1703 E. Mabel St., Tucson, AZ 85721, USA.

出版信息

Future Med Chem. 2010 Apr;2(4):619-46. doi: 10.4155/fmc.09.172.

Abstract

DNA G-quadruplexes are DNA secondary structures formed in specific G-rich sequences. DNA sequences that can form G-quadruplexes have been found in regions with biological significance, such as human telomeres and oncogene-promoter regions. DNA G-quadruplexes have recently emerged as a new class of novel molecular targets for anticancer drugs. Recent progress on structural studies of the biologically relevant G-quadruplexes formed in human telomeres and in the promoter regions of human oncogenes will be discussed, as well as recent advances in the design and development of G-quadruplex-interactive drugs. DNA G-quadruplexes can readily form in solution under physiological conditions and are globularly folded nucleic acid structures. The molecular structures of intramolecular G-quadruplexes appear to differ from one another and, therefore, in principle may be differentially regulated and targeted by different proteins and drugs.

摘要

DNA 四链体是在特定富含 G 的序列中形成的 DNA 二级结构。在具有生物学意义的区域,如人类端粒和致癌基因启动子区域,已经发现了可以形成 G-四链体的 DNA 序列。DNA 四链体最近成为一种新型抗癌药物的新型分子靶标。将讨论在人类端粒中形成的具有生物学相关性的 G-四链体和人类致癌基因启动子区域的结构研究的最新进展,以及 G-四链体相互作用药物的设计和开发的最新进展。DNA 四链体在生理条件下很容易在溶液中形成,并且是球状折叠的核酸结构。分子内 G-四链体的结构似乎彼此不同,因此原则上可能受到不同的蛋白质和药物的差异调节和靶向。

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