Literature DB >> 16610940

Gene expression profiling to monitor therapeutic and adverse effects of antisense therapies for Duchenne muscular dystrophy.

Peter A C 't Hoen1, Caroline G C van der Wees, Annemieke Aartsma-Rus, Rolf Turk, Aurélie Goyenvalle, Olivier Danos, Luis Garcia, Gert-Jan B van Ommen, Johan T den Dunnen, Judith C T van Deutekom.   

Abstract

OBJECTIVES: The objective of this study was to assess the utility of the gene expression profiling technique for the preclinical evaluation of drug efficacy and safety, taking a new therapeutic approach for Duchenne muscular dystrophy (DMD) as an example.
METHODS: Muscles from dystrophin-deficient (mdx) mice, a well-characterized animal model for DMD, were injected with antisense constructs that restore the open reading frame in the Dmd gene. Synthetic antisense oligonucleotides (AONs) complexed with different carriers to enhance cellular uptake and recombinant adeno-associated virus (rAAV)-expressed antisense sequences were evaluated. Muscular gene expression profiles were analyzed on oligonucleotide microarrays.
RESULTS: Polyethylenimine (PEI)-complexed AONs restored the reading frame slightly more effectively than uncomplexed, F127- or Optison-complexed AONs. However, PEI induced the expression of many immune genes, reflecting an aggravation of the inflammation present in untreated mdx mice. Expression profiles in Optison and F127-injected muscles were similar to those of saline treated muscles, implying that these carriers did not evoke adverse responses. Due to moderate levels of exon skipping, a significant shift toward wild-type expression levels was not detected. Injection with rAAV vectors resulted in much higher production of dystrophin and greatly improved the histological appearance of the muscle. Depending on the efficacy of the treatment, the expression of genes previously shown to be elevated in muscular dystrophies, partly or completely returned to wild-type expression levels. Reductions in inflammation and fibrosis were among the most prominent changes observed.
CONCLUSION: Expression profiling is a powerful tool for the evaluation of both desired and adverse effects of new pharmacological therapies. It is sensitive and detects changes that are not histologically visible. In addition, its ability to simultaneously monitor a large number of different biological processes not only reduces the number of different assays required in preclinical research and clinical trials, but may also assist in the early detection of potential side effects.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 16610940     DOI: 10.2217/14622416.7.3.281

Source DB:  PubMed          Journal:  Pharmacogenomics        ISSN: 1462-2416            Impact factor:   2.533


  11 in total

Review 1.  What has the mdx mouse model of Duchenne muscular dystrophy contributed to our understanding of this disease?

Authors:  Jennifer Manning; Dervla O'Malley
Journal:  J Muscle Res Cell Motil       Date:  2015-02-11       Impact factor: 2.698

2.  Prednisolone treatment does not interfere with 2'-O-methyl phosphorothioate antisense-mediated exon skipping in Duchenne muscular dystrophy.

Authors:  Ingrid E C Verhaart; Hans Heemskerk; Tatyana G Karnaoukh; Ingrid G M Kolfschoten; Anne Vroon; Gert-Jan B van Ommen; Judith C T van Deutekom; Annemieke Aartsma-Rus
Journal:  Hum Gene Ther       Date:  2012-01-26       Impact factor: 5.695

3.  The role of drug profiles as similarity metrics: applications to repurposing, adverse effects detection and drug-drug interactions.

Authors:  Santiago Vilar; George Hripcsak
Journal:  Brief Bioinform       Date:  2017-07-01       Impact factor: 11.622

4.  Polymersome delivery of siRNA and antisense oligonucleotides.

Authors:  Younghoon Kim; Manorama Tewari; J David Pajerowski; Shenshen Cai; Shamik Sen; Jason H Williams; Jason Williams; Shashank R Sirsi; Shashank Sirsi; Gordon J Lutz; Gordon Lutz; Dennis E Discher
Journal:  J Control Release       Date:  2008-11-12       Impact factor: 9.776

5.  Cationic PMMA nanoparticles bind and deliver antisense oligoribonucleotides allowing restoration of dystrophin expression in the mdx mouse.

Authors:  Paola Rimessi; Patrizia Sabatelli; Marina Fabris; Paola Braghetta; Elena Bassi; Pietro Spitali; Gaetano Vattemi; Giuliano Tomelleri; Lara Mari; Daniela Perrone; Alessandro Medici; Marcella Neri; Matteo Bovolenta; Elena Martoni; Nadir M Maraldi; Francesca Gualandi; Luciano Merlini; Marco Ballestri; Luisa Tondelli; Katia Sparnacci; Paolo Bonaldo; Antonella Caputo; Michele Laus; Alessandra Ferlini
Journal:  Mol Ther       Date:  2009-02-24       Impact factor: 11.454

6.  Circulating Biomarkers for Duchenne Muscular Dystrophy.

Authors:  Annemieke Aartsma-Rus; Pietro Spitali
Journal:  J Neuromuscul Dis       Date:  2015-07-22

7.  Saponins enhance exon skipping of 2'-O-methyl phosphorothioate oligonucleotide in vitro and in vivo.

Authors:  Mingxing Wang; Bo Wu; Sapana N Shah; Peijuan Lu; Qilong Lu
Journal:  Drug Des Devel Ther       Date:  2018-10-31       Impact factor: 4.162

8.  Differential Gene Expression Profiling of Dystrophic Dog Muscle after MuStem Cell Transplantation.

Authors:  Florence Robriquet; Aurélie Lardenois; Candice Babarit; Thibaut Larcher; Laurence Dubreil; Isabelle Leroux; Céline Zuber; Mireille Ledevin; Jack-Yves Deschamps; Yves Fromes; Yan Cherel; Laetitia Guevel; Karl Rouger
Journal:  PLoS One       Date:  2015-05-08       Impact factor: 3.240

9.  Multi-level omics analysis in a murine model of dystrophin loss and therapeutic restoration.

Authors:  Thomas C Roberts; Henrik J Johansson; Graham McClorey; Caroline Godfrey; K Emelie M Blomberg; Thibault Coursindel; Michael J Gait; C I Edvard Smith; Janne Lehtiö; Samir El Andaloussi; Matthew J A Wood
Journal:  Hum Mol Genet       Date:  2015-09-18       Impact factor: 6.150

10.  Poly(ester amine) Composed of Polyethylenimine and Pluronic Enhance Delivery of Antisense Oligonucleotides In Vitro and in Dystrophic mdx Mice.

Authors:  Mingxing Wang; Bo Wu; Jason D Tucker; Lauren E Bollinger; Peijuan Lu; Qilong Lu
Journal:  Mol Ther Nucleic Acids       Date:  2016-08-02       Impact factor: 10.183

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.