“…Figures 2 and 3 show possible modulations by CGA, although individual pathways in which CGA is involved have not necessarily been reported. Figure 2 illustrates CGA's downregulation of ROS [2,11,48,120,127], DNA damage [123], EGFR [127], Akt/phosphatidyl 3-inositol kinase (PI3K) [127], ERK1/2 [11,127], NF-κB [2,121,125,127,128], TNF-α [2,122], IL-1β [122], IL-8 [2,11], IL-6 [122], MMPs [2,11], COX-2 [125,128], Bcl-2 [10,129], mTOR [10,127], VEGF [126], and upregulation of AMPK [7,49]. Although CGA's upregulation of CaMKK and LKB1 shown in Figure 3 has not been determined yet, Park et al [130] reported upregulation of them by neochlorogenic acid, an isomer of CGA.…”