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In general, three different groups of agents were described in the past: (i) mAbs, either targeting the ligand HGF or the receptor Met, (ii) tyrosine kinase inhibitors, targeting the tyrosine kinase domain of Met (and mostly also the TK domain of other RTKs), (iii) a truncated, soluble Met receptor serving as decoy for HGF (44) and the competitive HGF antagonist NK4 (18)

Indirect criteria used to identify paracellular transport include the first-order kinetics in which the amount transported plotted as a function of concentration is linear, lacking the saturation typical of protein-mediated transport mechanisms [24, 30]

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