Preferred Label : Skeletal Muscle Hypertrophy Pathway;
NCIt related terms : Skeletal muscle hypertrophy is regulated via AKT/mTOR pathway;
Alternative definition : BIOCARTA: Skeletal muscle atrophies with disuse while with increased use and increased
load skeletal muscle exhibits hypertrophy, with an increase in the size of existing
muscle fibers. One signaling pathway involved in regulating skeletal muscle atrophy
and hypertrophy is the AKT/mTOR pathway. The mTOR pathway activity increases in response
to muscle activity during hypertrophy and decreases in activity during atrophy. Blocking
this pathway genetically or with the mTOR inhibitor rapamycin blocks hypertrophy and
genetic activation of the pathway induces hypertrophy. One agent that promotes muscle
hypertrophy is the growth factor IGF-1. IGF-1 activates AKT, GSK-3 beta, and mTOR
to promote hypertrophy. In contrast, the calcineurin pathway is not involved in hypertrophy
and is down-regulated by agents such as IGF-1 that promote hypertrophy. Calcineurin
may modulate other aspects of muscle function such as the development of slow muscle
fibers through transcriptional regulation. These pathways lead to regulation of protein
translation, with increased translation apparently acting as a key regulatory point
in skeletal muscle hypertrophy. Agents such as IGF-1 that stimulate skeletal muscle
hypertrophy may provide treatments for muscle atrophy and wasting. (This definition
may be outdated - see the DesignNote.);
NCIt note : The BIOCARTA Definition (ALT_DEFINITION) for this pathway concept was provided by
BioCarta. This property was not created by, nor is it maintained by the NCI Thesaurus
staff. Additionally, BioCarta is no longer updating its pathway data; thus, the BIOCARTA
Definition might be outdated or inaccurate. Please see the Terms and Conditions for
Use at http://www.biocarta.com/.;
Biocarta ID : h_igf1mtorpathway;
Origin ID : C39113;
UMLS CUI : C1519338;
Semantic type(s)
has_gene_product_element
pathway_has_gene_element