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Chinese Journal of Natural Medicines (English Ed.) ; (6): 607-612, 2014.
Article in English | WPRIM | ID: wpr-812227

ABSTRACT

AIM@#To investigate the active constituents of Lignum Sappan (Caesalpinia sappan L.) on growth-related signaling and cell mitosis.@*METHOD@#The influence of the ethyl acetate (EtOAc) extract of Lignum Sappan and its constituents on growth-related signaling were evaluated by a luciferase assay in cells stably-transfected with NF-κB, STAT1, or STAT3 responsive luciferase reporter plasmid. The inhibitory effect on the cell cycle was determined by flow cytometric analysis. The anti-tumor activities were assessed in vitro and in vivo.@*RESULTS@#The EtOAc extract of Lignum Sappan had inhibitory activities on growth-related signaling and cell mitosis. Three major active compounds were sappanchalcone, brazilin, and butein. Sappanchalcone blocked cell cycle progression in the G2/M phase, brazilin inhibited TNFα/NF-κB signaling, while butein inhibited IL-6/STAT3 signaling, as well as TNFα/NF-κB signaling. The three compounds all demonstrated cytotoxic activities against human tumor cells in vitro. In a S180 tumor cell-bearing mice model, the anti-tumor efficacy of the EtOAc extract was better than the individual compounds acting alone.@*CONCLUSION@#These results indicate that Lignum Sappan contains multiple active compounds with different antitumor activities, which act synergistically to enhance their anti-tumor effects. The EtOAc extract of Lignum Sappan may be better than individual active constituent as a novel medicine for the treatment of cancer.


Subject(s)
Animals , Humans , Male , Antineoplastic Agents, Phytogenic , Pharmacology , Therapeutic Uses , Benzopyrans , Pharmacology , Therapeutic Uses , Caesalpinia , Cell Cycle Checkpoints , Chalcones , Pharmacology , Therapeutic Uses , Hep G2 Cells , Interleukin-6 , Metabolism , Mice, Inbred BALB C , Mitosis , NF-kappa B , Metabolism , Phytotherapy , Plant Extracts , Pharmacology , Therapeutic Uses , STAT3 Transcription Factor , Metabolism , Sarcoma , Drug Therapy , Metabolism , Signal Transduction , Tumor Necrosis Factor-alpha , Metabolism
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