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Branched-chain amino-acid transaminase 1, cytosolic (BCAT1, or BCATc) is an enzyme primarily responsible for the first cytosolic step in the catabolism of branched-chain amino acids (leucine, isoleucine, valine), transferring the amino group to α-ketoglutarate to produce glutamate and the corresponding branched-chain α-keto acids[5][7]. BCAT1 is highly expressed in the central nervous system and in proliferating cells, including various tumors, and is inducible in immune cells upon stimulation[5][1]. By regulating branched-chain amino acid availability, BCAT1 impacts energy production, cell signaling (notably mTORC1 signaling), and antioxidant defense in cancer and immune cells[1][3][5]. Aberrant BCAT1 expression is associated with disease states such as cancer, neurodegeneration, and diabetes, making it a potential therapeutic target and biomarker in these contexts[3][5][7].
Reversible transamination of branched-chain amino acids (leucine, isoleucine, valine) with α-ketoglutarate to form glutamate and branched-chain α-keto acids Regulation of mTORC1 signaling through modulation of leucine availability in immune and cancer cells
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