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Structural insights into G-quadruplexes: towards new anticancer drugs

机译:对G-四链体的结构见解:开发新的抗癌药物

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摘要

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.
机译:DNA G四链体是在富含G的特定序列中形成的DNA二级结构。已经在具有生物学意义的区域,例如人端粒和癌基因启动子区域中发现了可以形成G-四链体的DNA序列。 DNA G-四链体最近已成为一种新型的抗癌药物分子靶标。将讨论在人类端粒和人类癌基因启动子区域形成的生物学相关G-四链体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方面的最新进展。 DNA G-四链体在生理条件下很容易在溶液中形成,并且是球形折叠的核酸结构。分子内G-四链体的分子结构似乎互不相同,因此,原则上可能会受到不同蛋白质和药物的差异调节和靶向。

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