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Introduction Conclusions Curcumin inhibits tumor growth and angiogenesis in an orthotopic mouse model of human pancreatic cancer Bimonte S.1; Barbieri A.2; Palma G.2; Rea D.2; Luciano A2., Arra C.2 and Izzo F.1 1 Hepatobiliary Unit, Istituto Nazionale per lo studio e la cura dei Tumori "Fondazione G. Pascale", - IRCCS-ITALIA Via Mariano Semmola, 80131, Naples, Italy; 2 INT Facility, Istituto Nazionale per lo studio e la cura dei Tumori "Fondazione G. Pascale", - IRCCS-ITALIA Via Mariano Semmola, 80131, Naples, Italy   Corresponding Author: Sabrina Bimonte mail:s.bimonte@istitutotumori.na.it Introduction Pancreatic cancer is a malignant neoplasm originating from transformed cells arising in tissues forming the pancreas. The best chemotherapeutic agent used to treat pancreatic cancer is the gemcitabine. However, gemcitabine treatment is associated with many side effects. Thus novel strategies involving less toxic agents for treatment of pancreatic cancer are necessary. Curcumin is one such agent that inhibits the proliferation and angiogenesis of a wide variety of tumor cells, through the modulation of many cell signalling pathways. In this study, we investigated whether curcumin plays antitumor effects in MIA PaCa-2 cells. In vitro studies showed that curcumin inhibits the proliferation and enhances apoptosis of MIA PaCa-2 cells. To test whether the antitumor activity of curcumin is also observed in vivo, we generated an orthotopic mouse model of pancreatic cancer by injection of MIA PaCa-2 cells in nude mice. We placed mice on diet containing curcumin at 0.6% for 6 weeks. In these treated mice tumors were smaller with respect to controls and showed a downregulation of the transcription nuclear factor NF-κB and NF-κB-regulated gene products. Overall, our data indicate that curcumin has a great potential in treatment of human pancreatic cancer through the modulation of NF-κB pathway. Curcumin inhibits the tumor growth in orthotopic mouse model of pancreatic cancer. (A) MacroFluo images of fluorescent analysis tumor area images control and treated mice. (B) Measurements of fluorescence per second depicting tumor volume at different time points using Macrofluo images, showed that the final tumor volumes on day 35 after the start of treatment is significantly decreased in the curcumin group compared with control (P = 0.00393). Curcumin inhibits proliferation and enhances apoptosis in MIA PaCa-2 cells. (a)–(f) Wound assay results show suppression of MIA PaCa-2 cell proliferation induced by curcumin at 48  h (b) With respect to controls. The results are the mean of total invaded areas of three distinct sections on the slide per 48  h. (P = 0.02, Mann-Whitney U test). (g) MTT assay results show a suppression of proliferation in pancreatic cancer cells treated with curcumin respect to control cells. Data are representative of two independent experiments (P value <0.05). (h) In vitro apoptosis assay by flow cytometry indicated that curcumin enhances apoptosis in MIA PaCa-2 cells. (i) EMSA results showes that curcumin suppresses activation of NF-κB in MIA PACA-2 cells. (j) In vitro apoptosis assay by flow cytometry indicates that silencing of NF-κB using siRNA κB is not able to potentiate the apoptotic effects of curcumin on MIA PaCa-2 cells. Curcumin inhibits NF-κB activation and downregulates NF-κB-regulated gene products in orthotopic pancreatic tumors. (A) EMSA assay performed on orthotopic tumor tissue samples showed the inhibition of NF-κB by curcumin. (B) Immunohistochemical analysis for nuclear COX-2 and VEGF showed the inhibition of COX-2 and VEGF expression in curcumin-treated group, compared to controls (Figure 3B), lower panels). Percentages indicate the positive staining for the given biomarker. (C) Western blot showing that curcumin inhibits the expression of NF-κB-dependent gene products VEGF, cyclin D1, MMP-9, COX-2, IKKα, and IKKβ in pancreatic tumor tissues. Samples from three animals in each group were analysed, and representative data are shown. β-Actin was used as loading control. Conclusions Curcumin has a great potential in treatment of human pancreatic cancer through the modulation of NF-κB pathway.