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The miRNA has been shown to inhibit tumor proliferation and migration by directly repressing c-Met expression and altering the signaling of downstream cell cycle-related proteins (Lee et al., 2017), miR-34a (Hong et al., in vitro via the Akt signaling pathway by targeting c-Met (Wan et al., The HGF/c-Met axis also contributes to drug resistance in lung cancer

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This is consistent with the approach used for tirzepatide starting doses and semaglutide initial dosing