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Strategies against Nonsense: Oxadiazoles as Translational Readthrough-Inducing Drugs (TRIDs). | LitMetric

Strategies against Nonsense: Oxadiazoles as Translational Readthrough-Inducing Drugs (TRIDs).

Int J Mol Sci

Dipartimento di Scienze e Tecnologie Biologiche, Chimiche e Farmaceutiche (STEBICEF), Università Degli Studi di Palermo, Viale delle Scienze Ed. 16-17, 90128 Palermo, Italy.

Published: July 2019

AI Article Synopsis

  • The review examines oxadiazoles as potential drugs for promoting full-length protein production in genetic diseases caused by nonsense mutations, which lead to premature stop signals in protein synthesis.
  • It discusses different classes of translational readthrough-inducing drugs (TRIDs), comparing their mechanisms, particularly focusing on new oxadiazole derivatives versus traditional aminoglycosides.
  • The article also highlights recent findings on the effectiveness of these new TRIDs in restoring the cystic fibrosis transmembrane regulator (CFTR) protein, and explores combined strategies to improve TRID outcomes while considering future prospects and challenges in drug development.

Article Abstract

This review focuses on the use of oxadiazoles as translational readthrough-inducing drugs (TRIDs) to rescue the functional full-length protein expression in mendelian genetic diseases caused by nonsense mutations. These mutations in specific genes generate premature termination codons (PTCs) responsible for the translation of truncated proteins. After a brief introduction on nonsense mutations and their pathological effects, the features of various classes of TRIDs will be described discussing differences or similarities in their mechanisms of action. Strategies to correct the PTCs will be presented, particularly focusing on a new class of Ataluren-like oxadiazole derivatives in comparison to aminoglycosides. Additionally, recent results on the efficiency of new candidate TRIDs in restoring the production of the cystic fibrosis transmembrane regulator (CFTR) protein will be presented. Finally, a prospectus on complementary strategies to enhance the effect of TRIDs will be illustrated together with a conclusive paragraph about perspectives, opportunities, and caveats in developing small molecules as TRIDs.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6651739PMC
http://dx.doi.org/10.3390/ijms20133329DOI Listing

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