Repository logo
  • English
  • ไทย
Log In
New user? Click here to register. Have you forgotten your password?
Communities & Collections
All of Mahidol IR
Mahidol Journals
Statistics
About Us
Customer Feedback
Deposit
  1. Home

Browsing by Author "Karen Anthony"

Filter results by typing the first few letters
Now showing 1 - 1 of 1
  • Results Per Page
  • Sort Options
  • No Thumbnail Available
    PublicationMetadata only
    A novel morpholino oligomer targeting ISS-N1 improves rescue of severe spinal muscular atrophy transgenic mice
    (2013-03-01) Haiyan Zhou; Narinder Janghra; Chalermchai Mitrpant; Rachel L. Dickinson; Karen Anthony; Loren Price; Ian C. Eperon; Stephen D. Wilton; Jennifer Morgan; Francesco Muntoni; UCL Institute of Child Health; Mahidol University; University of Western Australia; University of Leicester
    In the search for the most efficacious antisense oligonucleotides (AOs) aimed at inducing SMN2 exon 7 inclusion, we systematically assessed three AOs, PMO25 (-10,-34), PMO18 (-10,-27), and PMO20 (-10,-29), complementary to the SMN2 intron 7 splicing silencer (ISS-N1). PMO25 was the most efficacious in augmenting exon 7 inclusion in vitro in spinal muscular atrophy (SMA) patient fibroblasts and in vitro splicing assays. PMO25 and PMO18 were compared further in a mouse model of severe SMA. After a single intracerebroventricular (ICV) injection in neonatal mice, PMO25 increased the life span of severe SMA mice up to 30-fold, with average survival greater by 3-fold compared with PMO18 at a dose of 20 μg/g and 2-fold at 40 μg/g. Exon 7 inclusion was increased in the CNS but not in peripheral tissues. Systemic delivery of PMO25 at birth achieved a similar outcome and produced increased exon 7 inclusion both in the CNS and peripherally. Systemic administration of a 10-μg/g concentration of PMO25 conjugated to an octaguanidine dendrimer (VMO25) increased the life span only 2-fold in neonatal type I SMA mice, although it prevented tail necrosis in mild SMA mice. Higher doses and ICV injection of VMO25 were associated with toxicity. We conclude that (1) the 25-mer AO is more efficient than the 18-mer and 20-mer in modifying SMN2 splicing in vitro; (2) it is more efficient in prolonging survival in SMA mice; and (3) naked Morpholino oligomers are more efficient and safer than the Vivo-Morpholino and have potential for future SMA clinical applications. © 2013, Mary Ann Liebert, Inc.

Contact Us

Mahidol University Library and Knowledge Center.

Mahidol University Repository Division, Scholarly Resources Department

Office Hour: Monday-Friday 08.30-12.00 and 13.00-16.30 hrs.
Phutthamonthon Sai 4 Rd. Salaya, Nakhon Pathom 73170, Thailand
The office: +66 (2) 800 2680 ext.4306
thipsuda.van@mahidol.ac.th
https://repository.li.mahidol.ac.th
Except where otherwise noted, content on this site is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International license.
  • Privacy Notice
  • Term of use