“…These studies observed modulation in the expression of several proteins and genes, including an upregulation in the expression of vascular endothelial growth factor (VEGF), transformative growth factor-β (TGF-β), metalloproteinase-2 (MPP-2), metalloproteinase-9 (MMP-9), heat shock protein-27 (HSP27), HSP60, hepatocyte growth factor (HGF), chemokine-16 (CXCL16), hypoxia-inducible factor 1-alpha (HIF-1α), keratinocyte growth factor (KGF), leptin, interleukin-8 (IL-8), TGF-α, Dnmt3a, cytokeratin-10 (Krt-10), cytokeratin-17 (Krt-17), platelet-derived growth factor (PDGF), and proliferating cell nuclear antigen. 16,19,20,23,24,29,[32][33][34][35]40 On the other hand, there was a decrease in tissue metalloproteinase inhibitor 1 e 2 (TIMP-1/TIMP-2) and cyclooxygenase-2 (COX-2) e cytokeratin-1 (Krt-1). 19,33,43 As for the studies using blue LEDs, a modulation in the overexpression of tissue inhibitors of metalloproteinase 1 and 2 (TIMP-1, TIMP-2), dipeptidylpeptidase-IV (DPP-IV), neuregulin1-b1 (NRG1-b1), placental growth factor, HGF e KGF, 19,23,32 and protein reduction MMP-2 e MMP-9.…”