Fluorescent light-up acridine orange derivatives bind and stabilize KRAS-22RT G-quadruplex
Language English Country France Media print-electronic
Document type Journal Article
PubMed
29129745
DOI
10.1016/j.biochi.2017.11.004
PII: S0300-9084(17)30284-5
Knihovny.cz E-resources
- Keywords
- Acridine orange ligands, Fluorescent probes, G-quadruplex, KRAS promoter, NMR spectroscopy,
- MeSH
- Acridine Orange chemistry metabolism pharmacology MeSH
- Biological Transport MeSH
- Fluorescent Dyes chemistry metabolism pharmacology MeSH
- G-Quadruplexes drug effects MeSH
- HeLa Cells MeSH
- Intracellular Space metabolism MeSH
- Humans MeSH
- Ligands MeSH
- Cell Proliferation drug effects MeSH
- Proto-Oncogene Proteins p21(ras) genetics MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Acridine Orange MeSH
- Fluorescent Dyes MeSH
- KRAS protein, human MeSH Browser
- Ligands MeSH
- Proto-Oncogene Proteins p21(ras) MeSH
KRAS is often found mutated in lethal cancers and should be an important target for anticancer drug development. However, no effective inhibitor has been reported so far, prompting the scientific community to describe the RAS proteins as nearly "undruggable". Recent approaches developed to modulate KRAS protein expression comprises the targeting of G-quadruplex (G4) structures formed within the nuclease hypersensitive element of KRAS promoter region, by designing small and specific ligands to stabilize the tertiary fold and reduce gene expression. In this work, we report in vitro and in silico studies of novel acridine orange (AO) derivatives (C3-C8), developed as G4 stabilizing agents. The results show that the ligands bind with high affinity and stabilize KRAS22-RT G4 with modest specificity over duplex DNA. The most promising ligand C8 stabilizes the structure by ≈ 40 °C. Molecular docking using NMR-derived distance restraints reveal atomic details about the ligand structural features in the interaction with KRAS22-RT G4. In vitro studies with HeLa cells show that the ligands are cytotoxic with IC50 values between 0.9 μM and 5.7 μM. Moreover, the ligands tend to localize in the nucleus as shown by confocal fluorescence microscopy. Overall, these results show that the reported AO ligands display favourable properties as G4 ligands and this study provides structural detail for the development of lead KRAS G4 ligands.
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