{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,27]],"date-time":"2026-09-27T12:58:49Z","timestamp":1790513929477,"version":"4.1.0"},"reference-count":62,"publisher":"Wiley","issue":"11","license":[{"start":{"date-parts":[[2019,8,23]],"date-time":"2019-08-23T00:00:00Z","timestamp":1566518400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["faseb.onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["The FASEB Journal"],"published-print":{"date-parts":[[2019,11]]},"abstract":"<jats:p>\n                    The deleterious effects of statins on skeletal muscle are well known, but the mechanism associated with these effects remains unresolved. Statins are associated with mitochondrial damage, which may contribute to muscle myopathy. Here we demonstrate that simvastatin induces mitophagy in skeletal muscle cells and hypothesized that attenuating this process by silencing the mitophagy adapter p62\/sequestosome\u20101 (SQSTM1) might mitigate myotoxicity. Surprisingly, silencing p62\/SQSTM1 in differentiated C2C12 muscle cells exacerbated rather than attenuated myotoxicity. This inhibition of mitophagy in the face of statin challenge correlated with increased release of cytochrome c to the cytosol, activation of caspase\u20103, and lactate dehydrogenase (LDH) release. Correspondingly, targeted knockdown of Parkin, a canonical E3 ubiquitin ligase important for mitophagy, mirrored the effects of p62\/SQSTM1 silencing. To corroborate these findings\n                    <jats:italic>in vivo<\/jats:italic>\n                    , we treated Parkin knockout mice with simvastatin for 2 wk. In line with our findings in vitro, these mitophagy\u2010compromised mice displayed reduced spontaneous activity, loss of grip strength, and increased circulating levels of muscle damage marker LDH. Our findings demonstrate that mitophagy is an important mechanism to resist statin\u2010induced skeletal muscle damage.\u2014Ramesh, M., Campos, J. C., Lee, P., Song, Y., Hernandez, G., Sin, J., Tucker, K. C., Saadaeijahromi, H., Gurney, M., Ferreira, J. C. B., Andres, A. M. Mitophagy protects against statin\u2010mediated skeletal muscle toxicity. FASEB J. 33, 11857\u201011869 (2019).\n                    <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" xlink:href=\"http:\/\/www.fasebj.org\">www.fasebj.org<\/jats:ext-link>\n                  <\/jats:p>","DOI":"10.1096\/fj.201900807rr","type":"journal-article","created":{"date-parts":[[2019,7,31]],"date-time":"2019-07-31T19:21:27Z","timestamp":1564600887000},"page":"11857-11869","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":16,"title":["EXPRESSION OF CONCERN: Mitophagy protects against statin\u2010mediated skeletal muscle toxicity"],"prefix":"10.1096","volume":"33","author":[{"given":"idula","family":"Ramesh","sequence":"first","affiliation":[{"name":"Donald P. Shiley BioScience Center San Diego State University San Diego California USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Juliane C.","family":"Campos","sequence":"additional","affiliation":[{"name":"Cedars\u2010Sinai Medical Center Los Angeles California USA"},{"name":"Institute of Biomedical Sciences University of Sao Paulo Sao Paulo Brazil"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Pamela","family":"Lee","sequence":"additional","affiliation":[{"name":"Donald P. Shiley BioScience Center San Diego State University San Diego California USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yang","family":"Song","sequence":"additional","affiliation":[{"name":"Cedars\u2010Sinai Medical Center Los Angeles California USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Genaro","family":"Hernandez","sequence":"additional","affiliation":[{"name":"Donald P. 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