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96,97 Moreover, the ME1 protein is hypophosphorylated at S336 and hyperacetylated at K337 by PGAM family member 5 and acetyl-CoA acetyltransferase, respectively, resulting in ME1 translocation from mitochondria to the cytosol, dimerization and activation, thus strongly promoting NADPH generation and tumorigenesis

PRMT1 catalyzes the mono- and asymmetric dimethylation of arginine residues, thereby influencing protein function, stability, and subcellular localization [14, 15]

Mechanism investigation focuses on Akt-eNOS axis activation and sustained NO synthesis for neovascularization