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ROS promote epithelial-mesenchymal transition (EMT), migration, invasion (e.g., by regulating MMPs), and survival of circulating tumor cells from anoikis and oxidative stress within the blood circulation [32]
The function of the fatty-acid oxidation pathway in fibroblast cultures and biomarkers for abnormalities in non-mitochondrial fatty-acid metabolism were not consistently abnormal across the subgroup of ASD children, consistent with the notion that the abnormalities in fatty-acid metabolism found in this subgroup of children with ASD were secondary to TCAC abnormalities
10.1016/j.juro.2006.10.065 40 GressnerA
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