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ABSTRACT: Background
Skeletal muscle atrophy is a common clinical manifestation of various neurotrauma and neurological diseases. In addition to the treatment of primary neuropathies, it is a clinical condition that should be investigated. FoxO3 activation is an indispensable mechanism in denervation-induced muscle atrophy; however, upstream factors that control FoxO3 expression and activity have not been fully elucidated. N6 -methyladenosine (m6 A) methylation is a novel mode of epitranscriptional gene regulation that affects several cellular processes. However, the biological significance of m6 A modification in FoxO3-dependent atrophy is unknown.Methods
We performed gain-of-function and loss-of-function experiments and used denervation-induced musc
SUBMITTER: Liu Y
PROVIDER: S-EPMC8978003 | biostudies-literature | 2022 Apr
REPOSITORIES: biostudies-literature