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We have previously shown that mitogen-activated protein kinase (MAPK) and phosphatidylinositol 3-kinase (PI3K) are the major downstream signalling molecules that mediate HGF-induced proliferation and migration of cancer and endothelial cells

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IR induced metabolic disturbances lead to degradation of brain function, and prolonged uncontrolled high blood glucose levels adversely affect a variety of metabolic pathways such as oxidative stress, formation of advanced glycosylation end products (AGEs), and protein kinase C activation, while metabolic disturbances inducing cerebral microvascular damage affect the extent of cognitive impairment (1, 7)

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