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Interestingly, their in silico molecular docking results indicated that sitagliptin may exhibit putative binding affinities with the DPP4/CTNNB1/MET signatures, surpassing those of standard inhibitors for these genes

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Its research profile makes it relevant to controlled investigations involving methylation-linked metabolism, energy-balance signaling, metabolic stress response, adipose-associated cellular systems, and cellular adaptation under nutrient-sensitive conditions