Literature DB >> 20409719

Repairing faulty genes by aminoglycosides: development of new derivatives of geneticin (G418) with enhanced suppression of diseases-causing nonsense mutations.

Igor Nudelman1, Dana Glikin, Boris Smolkin, Mariana Hainrichson, Valery Belakhov, Timor Baasov.   

Abstract

New pseudo-di- and pseudo-trisaccharide derivatives of the aminoglycoside drug G418 were designed, synthesized and their ability to readthrough nonsense mutations was examined in both in vitro and ex vivo systems, along with the toxicity tests. Two novel lead structures, NB74 and NB84, exhibiting significantly reduced cell toxicity and superior readthrough efficiency than those of gentamicin, were discovered. The superiority of new leads was demonstrated in six different nonsense DNA-constructs underling the genetic diseases cystic fibrosis, Duchenne muscular dystrophy, Usher syndrome and Hurler syndrome.

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Year:  2010        PMID: 20409719     DOI: 10.1016/j.bmc.2010.03.060

Source DB:  PubMed          Journal:  Bioorg Med Chem        ISSN: 0968-0896            Impact factor:   3.641


  64 in total

1.  Characterization of new-generation aminoglycoside promoting premature termination codon readthrough in cancer cells.

Authors:  Laure Bidou; Olivier Bugaud; Valery Belakhov; Timor Baasov; Olivier Namy
Journal:  RNA Biol       Date:  2017-02-01       Impact factor: 4.652

2.  Post-transcriptionally regulated expression system in human xenogeneic transplantation models.

Authors:  Hui-Ling Rose Lee; Chiann-Chyi Chen; Timor Baasov; Yacov Ron; Joseph P Dougherty
Journal:  Mol Ther       Date:  2011-05-17       Impact factor: 11.454

Review 3.  Chemotherapeutics overcoming nonsense mutation-associated genetic diseases: medicinal chemistry of negamycin.

Authors:  Akihiro Taguchi; Keisuke Hamada; Yoshio Hayashi
Journal:  J Antibiot (Tokyo)       Date:  2017-09-27       Impact factor: 2.649

4.  A breakthrough in readthrough? Could geneticin lead the way to effective treatment for cystinosis nonsense mutations?

Authors:  Julian Midgley
Journal:  Pediatr Nephrol       Date:  2019-01-08       Impact factor: 3.714

Review 5.  Clarifying lysosomal storage diseases.

Authors:  Mark L Schultz; Luis Tecedor; Michael Chang; Beverly L Davidson
Journal:  Trends Neurosci       Date:  2011-06-30       Impact factor: 13.837

Review 6.  Therapeutics based on stop codon readthrough.

Authors:  Kim M Keeling; Xiaojiao Xue; Gwen Gunn; David M Bedwell
Journal:  Annu Rev Genomics Hum Genet       Date:  2014-04-18       Impact factor: 8.929

7.  Cyclin-dependent kinase 4 may be expressed as multiple proteins and have functions that are independent of binding to CCND and RB and occur at the S and G 2/M phases of the cell cycle.

Authors:  Yuan Sun; Xiaomin Lou; Min Yang; Chengfu Yuan; Ling Ma; Bing-Kun Xie; Jian-Min Wu; Wei Yang; Steven Xj Shen; Ningzhi Xu; D Joshua Liao
Journal:  Cell Cycle       Date:  2013-09-24       Impact factor: 4.534

Review 8.  Nonsense-mediated decay in genetic disease: friend or foe?

Authors:  Jake N Miller; David A Pearce
Journal:  Mutat Res Rev Mutat Res       Date:  2014-05-28       Impact factor: 5.657

9.  In vitro read-through of phenylalanine hydroxylase (PAH) nonsense mutations using aminoglycosides: a potential therapy for phenylketonuria.

Authors:  Gladys Ho; Juergen Reichardt; John Christodoulou
Journal:  J Inherit Metab Dis       Date:  2013-03-27       Impact factor: 4.982

10.  New inducible genetic method reveals critical roles of GABA in the control of feeding and metabolism.

Authors:  Fantao Meng; Yong Han; Dollada Srisai; Valery Belakhov; Monica Farias; Yong Xu; Richard D Palmiter; Timor Baasov; Qi Wu
Journal:  Proc Natl Acad Sci U S A       Date:  2016-03-14       Impact factor: 11.205

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