Publications by authors named "J L Mergny"

Understanding the mechanisms of carcinogenesis is essential to combat cancer. The search for alternative targets for anticancer therapy has gained interest, particularly when focused on upstream pathways. This strategy is particularly relevant when the encoded target proteins are known - or believed - to be "undruggable", as has been reported for the B-MYB oncogene.

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Retroviruses are among the most extensively studied viral families, both historically and in contemporary research. They are primarily investigated in the fields of viral oncogenesis, reverse transcription mechanisms, and other infection-specific aspects. These include the integration of endogenous retroviruses (ERVs) into host genomes, a process widely utilized in genetic engineering, and the ongoing search for HIV/AIDS treatment.

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G-quadruplexes (G4s) are four-stranded structures formed by guanine-rich sequences. While their structures, properties, and applications have been extensively studied, an understanding of their folding processes remains limited. In this study, we investigated the folding of the sequence d[(GT)G] in potassium solutions, focusing on the impact of a folding intermediate on the overall folding process.

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Article Synopsis
  • - G-quadruplexes (G4s) in RNA are becoming important targets for cancer and disease therapies, with GG motifs being more common than GGG motifs in RNA sequences.
  • - Recent findings indicate that DNA cannot make stable two-tetrad G4 structures, raising questions about the stability of RNA GG motifs and their potential regulatory functions.
  • - This study reveals that RNA GG motifs typically don't form stable intramolecular G4s by themselves; instead, they need to dimerize to create stable structures, which may play a role in RNA aggregation during cellular stress.
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Novel 1,10-phenanthroline-2,9-bistriazoles derivatives have been synthesized by copper-catalyzed azide/alkyne cycloaddition reactions and assessed for their ability to bind and stabilize G-quadruplex (G4) structures. Ten novel compounds were evaluated using Förster resonance energy transfer (FRET) melting, circular dichroism (CD), and fluorescence spectroscopy on several G4 sequences. Biophysical characterization led to the identification of compounds 4 a, 4 b, and 5 b as good G4 ligands of KRAS G4 sequences.

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