Published: July 01, 2011
miRagen Therapeutics and Collaborators Identify Key Role for miR-133a as a Modulator of Skeletal Muscle Disorder
BOULDER, Colo. - (BUSINESS WIRE) - miRagen Therapeutics, Inc., a biopharmaceutical company focused on
improving patients' lives by developing innovative microRNA
(miRNA)-based therapeutics for cardiovascular and muscle disease,
announced today that new preclinical data reveal an essential role for
miR-133a in the maintenance of adult skeletal muscle structure and
function. The study suggests that miR-133a is a modulator of the
development of human centronuclear myopathy (CNM), a rare condition
affecting skeletal muscles. The research, licensed by miRagen
Therapeutics, was conducted by researchers at the University of Texas
Southwestern Medical Center and Virginia Polytechnic Institute and State
University. Results of the study were published today in the August
issue of The Journal of Clinical Investigation.
Human CNMs are a group of congenital diseases of muscle tissue
characterized by muscle weakness and abnormal centralization of nuclei
in muscle myofibers. In this study, adult mice lacking miR-133a
developed progressive CNM, as well as mitochondrial dysfunction and
fast-to-slow myofiber conversion. These findings demonstrate an
essential role for miR-133a in the maintenance of adult skeletal muscle
structure, function, bioenergetics, and myofiber identity; they also
strongly suggest that miR-133a is a potential modulator of CNM.
"The similarities in the skeletal muscle abnormalities found in the
miR-133a deficient mice and human CNM patients suggest that miR-133a may
play a role in the disease," said Eric N. Olson, Ph.D., Chief Scientific
Advisor and Co-founder of miRagen Therapeutics, Inc. "The findings
further underscore the potential of microRNA modulation as a novel
therapeutic approach to treat skeletal muscle diseases."
"We are very excited by the publication of these results that further
demonstrate the important role of miR-133a in maintaining normal
structure and function of adult skeletal muscle," said William S.
Marshall, Ph.D., President and Chief Executive Officer of miRagen
Therapeutics, Inc. "These findings ultimately enhance our commitment to
developing innovative microRNA-based therapeutics to treat patients with
debilitating muscle diseases."
About microRNAs: MicroRNAs have emerged as an important class of
small RNAs encoded in the genome. They act to control the expression of
sets of genes and entire pathways and are thus thought of as master
regulators of gene expression. Recent studies have demonstrated that
microRNAs are associated with many disease processes. Because they are
single molecular entities that dictate the expression of fundamental
regulatory pathways, microRNAs represent potential drug targets for
controlling many biologic and disease processes.
About miRagen Therapeutics: miRagen Therapeutics, Inc., was
founded in 2007 to develop innovative microRNA-based therapeutics for
cardiovascular and muscle disease. Only recently discovered, microRNAs
are short, single-stranded RNA molecules encoded in the genome that
regulate gene expression and play a vital role in influencing
cardiovascular and muscle disease. Cardiovascular disease is the leading
cause of death globally and represents an enormous burden on global
healthcare systems. Principally funded through venture capital
investments, miRagen combines world recognized leadership in
cardiovascular medicine with unprecedented in-house expertise in
microRNA biology and chemistry. For more information, please visit www.miragentherapeutics.com.

Scout Investor Relations for miRagen
Anna Sussman,
303-907-5358
anna@scoutir.com
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