[1] Simonetti O, Lucarini G, Brancorsini D, et al. Immunohistochemical expression of vascular endothelial growth factor, matrix metalloproteinase 2, and matrix metalloproteinase 9 in cutaneous melanocytic lesions. Cancer, 2002, 95: 1963-1970. [2] Liu B, Earl HM, Baban D,et al. Melanoma cell lines express VEGF receptor KDR and respond to exogenously added VEGF. Biochem Biophys Res Commun, 1995, 217: 721-727. [3] Gorski DH, Leal AD, Goydos JS. Differential expression of vascular endothelial growth factor-A isoforms at different stages of melanoma progression. J Am Coll Surg, 2003, 197: 408-418. [4] Schadendorf D. Gene-based therapy of malignant melanoma. Semin Oncol, 2002, 29: 503-512. [5] Reich SJ, Fosnot J, Kuroki A,et al. Small interfering RNA (siRNA)targeting VEGF effectively inhibits ocular neovascularization in a mouse model. Mol Vis, 2003, 9: 210-216. [6] Pricop L, Redecha P, Teillaud JL,et al. Differential modulation of stimulatory and inhibitory Fc gamma receptors on human monocytes by Th1 and Th2 cytokines. J Immunol, 2001, 166: 531-537. [7] Anan K, Morisaki T, Katano M,et al. Vascular endothelial growth factor and platelet-derived growth factor are potential angiogenic and metastatic factors in human breast cancer. Surgery, 1996, 119:333-339. [8] Hofmann UB, Westphal JR, Waas ET, et al. Matrix metalloproteinases in human melanoma cell lines and xenografts: increased expression of activated matrix metalloproteinase-2 (MMP-2) correlates with melanoma progression. Br J Cancer, 1999, 81: 774-782. |