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- W1967544564 abstract "Skeletal muscle atrophy occurs in multiple clinical settings, including cancer, AIDS and sepsis, and is caused in part by an increase in the rate of ATP-dependent ubiquitin-mediated proteolysis. The expression of two recently identified genes encoding ubiquitin-protein ligases, MAFbx/Atrogin-1 and MuRF1, has been shown to increase during muscle atrophy. Mouse knockout studies have demonstrated that MAFbx and MuRF1 are required for muscle atrophy, and thus might be targets for clinical intervention. A second strategy for blocking atrophy involves the stimulation of pathways leading to skeletal muscle hypertrophy. Insulin-like growth factor 1 (IGF-1) is a protein growth factor that can induce skeletal muscle hypertrophy by activating the phosphatidylinositol 3-kinase (PI3K)-Akt pathway. The pathways modulating hypertrophy and atrophy will be further discussed, to highlight potential targets for clinical intervention." @default.
- W1967544564 created "2016-06-24" @default.
- W1967544564 creator A5054558716 @default.
- W1967544564 date "2003-08-01" @default.
- W1967544564 modified "2023-10-10" @default.
- W1967544564 title "Molecular mechanisms modulating muscle mass" @default.
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- W1967544564 doi "https://doi.org/10.1016/s1471-4914(03)00138-2" @default.
- W1967544564 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/12928036" @default.
- W1967544564 hasPublicationYear "2003" @default.
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