Sugiyama, Recent Progress of Targeted G-Quadruplex-Preferred Ligands Toward Cancer Therapy

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  • 朝光, 世煌
    Department of Chemistry, Graduate School of Science Kyoto University
  • 小幡, 俊介
    Department of Chemistry, Graduate School of Science Kyoto University
  • 余, 祖滔
    Department of Chemistry, Graduate School of Science Kyoto University
  • 板東, 俊和
    Department of Chemistry, Graduate School of Science Kyoto University
  • 杉山, 弘
    Department of Chemistry, Graduate School of Science Kyoto University･Institute for Integrated Cell-Material Science (WPI-iCeMS) Kyoto University

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  • Recent Progress of Targeted G-Quadruplex-Preferred Ligands Toward Cancer Therapy

抄録

A G-quadruplex (G4) is a well-known nucleic acid secondary structure comprising guanine-rich sequences, and has profound implications for various pharmacological and biological events, including cancers. Therefore, ligands interacting with G4s have attracted great attention as potential anticancer therapies or in molecular probe applications. To date, a large variety of DNA/RNA G4 ligands have been developed by a number of laboratories. As protein-targeting drugs face similar situations, G-quadruplex-interacting drugs displayed low selectivity to the targeted G-quadruplex structure. This low selectivity could cause unexpected effects that are usually reasons to halt the drug development process. In this review, we address the recent research on synthetic G4 DNA-interacting ligands that allow targeting of selected G4s as an approach toward the discovery of highly effective anticancer drugs.

収録刊行物

  • Molecules

    Molecules 24 (3), 429-, 2019-01-24

    NLM (Medline)

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