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1k), suggesting that CAR T cells from LTR preferentially shunt HK glycolytic metabolites to the pentose phosphate pathway (PPP) rather than glycolysis, and by CPT1A could convert long-chain fatty acids into acylcarnitines for shuttling into the mitochondrial matrix for subsequent oxidation, previously associated with increased basal and maximal mitochondrial respiration 5,6,7,8

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Increased expression of the FMO3 gene could be a culprit in atherosclerosis and CVD.8 FMO3 may have adverse effects on blood lipids and glucose independently of TMAO formation, although more research is needed.15 Also, in the liver, trimethyllysine (TML), a modified amino acid, can be converted to GBB and then to carnitine and potentially to TMA and TMAO

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10.3390/nu8100613 23 Global Cancer Observatory (2022)