期刊
CANCER
卷 104, 期 6, 页码 1322-1331出版社
WILEY
DOI: 10.1002/cncr.21300
关键词
proliferation; apoptosis; angiogenesis; curcumin
类别
资金
- NCI NIH HHS [1 P20 CA101936-01] Funding Source: Medline
BACKGROUND. Because a role for nuclear factor-kappa B (NF-kappa B) has been implicated in the pathogenesis of pancreatic carcinoma, this transcription factor is a potential target for the treatment of this devastating disease. Curcumin (diferuloylmethane) is a phytochemical with potent NF-kappa B-inhibitory activity. It is pharmacologically safe, but its bioavailability is poor after oral administration. METHODS. The authors encapsulated curcumin in a liposomal delivery system that would allow intravenous administration. They studied the in vitro and in vivo effects of this compound on proliferation, apoptosis, signaling, and angiogenesis using human pancreatic carcinoma cells. NF-kappa B was constitutively active in all human pancreatic carcinoma cell lines evaluated and liposomal curcumin consistently suppressed NF-kappa B binding (electrophoretic mobility gel shift assay) and decreased the expression of NF-kappa B-regulated gene products, including cyclooxygenase-2 (immunoblots) and interleukin-8 (enzyme-linked immunoassay), both of which have been implicated in tumor growth/invasiveness. These in vitro changes were associated with concentration and time-dependent antiproliferative activity (3-[4,5-dimethyithiazol-2-yl]2,5-diphetiyltetrazolium bromide assay [MTT assay]) and proapoptotic effects (annexin V/propidium iodide staining [fluorescence-activated cell sorting] and polyadetiosine-5'-diphosphate-ribose-polymerase cleavage). RESULTS. The activity of liposomal curcumin was equal to or better than that of free curcumin at equimolar concentrations. In vivo, curcumin suppressed pancreatic carcinoma growth in murine xenograft models and inhibited tumor angiogenesis. CONCLUSIONS. Liposomal curcumin down-regulated the NF-kappa B machinery, suppressed growth, and induced apoptosis of human pancreatic cells in vitro. Antitumor and antiangiogenesis effects were observed in vivo. The experiments in the Current Study provide a biologic rationale for treatment of patients suffering from pancreatic carcinoma with this nontoxic phytochemical encapsulated in liposomes for systemic delivery.
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