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Skelet Muscle. 2014 Feb 1;4(1):4. doi: 10.1186/2044-5040-4-4.

High-throughput screening identifies inhibitors of DUX4-induced myoblast toxicity.

Author information

1
Lillehei Heart Institute, 312 Church St. SE, Minneapolis, MN 55455, USA.
2
Department of Pediatrics, University of Minnesota, Nils Hasselmo Hall, 312 Church St. S.E, Minneapolis, MN 55455, USA.
3
Present Address: Faculty of Medical Sciences, University Goce Delčev - Štip, Krste Misirkov b.b, 2000 Štip, R. Macedonia.
4
Institute for Therapeutics Discovery and Development, University of Minnesota, 717 Delaware St. SE, Minneapolis, MN 55455, USA.
#
Contributed equally

Abstract

BACKGROUND:

Facioscapulohumeral muscular dystrophy (FSHD) is caused by epigenetic alterations at the D4Z4 macrosatellite repeat locus on chromosome 4, resulting in inappropriate expression of the DUX4 protein. The DUX4 protein is therefore the primary molecular target for therapeutic intervention.

METHODS:

We have developed a high-throughput screen based on the toxicity of DUX4 when overexpressed in C2C12 myoblasts, and identified inhibitors of DUX4-induced toxicity from within a diverse set of 44,000 small, drug-like molecules. A total of 1,280 hits were then subjected to secondary screening for activity against DUX4 expressed by 3T3 fibroblasts, for absence of activity against the tet-on system used to conditionally express DUX4, and for potential effects on cellular proliferation rate.

RESULTS:

This allowed us to define a panel of 52 compounds to use as probes to identify essential pathways of DUX4 activity. We tested these compounds for their ability to protect wild-type cells from other types of cell death-inducing insults. Remarkably, we found that 60% of the DUX4 toxicity inhibitors that we identified also protected cells from tert-butyl hydrogen peroxide, an oxidative stress-inducing compound. Compounds did not protect against death induced by caspase activation, DNA damage, protein misfolding, or ER stress. Encouragingly, many of these compounds are also protective against DUX4 expression in human cells.

CONCLUSION:

These data suggest that oxidative stress is a dominant pathway through which DUX4-provoked toxicity is mediated in this system, and we speculate that enhancing the oxidative stress response pathway might be clinically beneficial in FSHD.

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