Inhibitory effects of docosahexaenoic acid on the growth of incubated human pancreatic cancer cell lines
Zhu Sheng-ta
Abstract
Zhu Sheng-ta
Abstract
Objective To investigate the effects of docosahexaenoic acid(DHA) on the growth of human pancreatic cancer cell lines.Methods Human pancreatic cancer cell lines Patu8988 and SW1990 were treated with DHA.The cell proliferation was evaluated by MTT assay.Cell cycle,apoptosis,and cyclooxygenase-2 expression were evaluated by flow cytometry.Results After incubation of pancreatic cancer cell with DHA for 24 to 72 hours,cell proliferation significantly decreased(P0.01) and apoptosis increased,both of which were timedependent and dose-dependent.After incubation with 50μg/ml DHA for 24 hours,cyclooxygenase-2 expression of pancreatic cancer cell lines significantly decreased(P0.05).Conclusions DHA can inhibit the growth of human pancreatic cancer cells via decreasing cell proliferation and inducing apoptosis.These effects may be associated with the decrease of cyclooxygenase-2 expression.
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Objective To investigate the effects of docosahexaenoic acid(DHA) on the growth of human pancreatic cancer cell lines.Methods Human pancreatic cancer cell lines Patu8988 and SW1990 were treated with DHA.The cell proliferation was evaluated by MTT assay.Cell cycle,apoptosis,and cyclooxygenase-2 expression were evaluated by flow cytometry.Results After incubation of pancreatic cancer cell with DHA for 24 to 72 hours,cell proliferation significantly decreased(P0.01) and apoptosis increased,both of which were timedependent and dose-dependent.After incubation with 50μg/ml DHA for 24 hours,cyclooxygenase-2 expression of pancreatic cancer cell lines significantly decreased(P0.05).Conclusions DHA can inhibit the growth of human pancreatic cancer cells via decreasing cell proliferation and inducing apoptosis.These effects may be associated with the decrease of cyclooxygenase-2 expression.
Key concepts: Docosahexaenoic acid, Pancreatic cancer, Apoptosis, Cell growth, Cell cycle, Cell culture, MTT assay, Flow cytometry