2011•Journal of Medical Science in Central South ChinaRequires access

Effects of Casticin on the Growth and Apoptosis of Colon Carcinoma Cell Line SW480

Jianguo Cao

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Abstract

Objective To observe the effect of casticin(CAS)on the growth and apoptosis of human colon cancer SW480 cells.Methods Human colon cancer SW480 cells were cultured in vitro.The capability of anchoring dependent growth in SW480 cells was determined using agar colony formation assay.Flow cytometry(FCM)analysis after PI staining and(FCM)was used to examine apoptosis rate in SW480 cells.Western Blotting was used to analyze the expression of DR5 and NF-κB(p65)protein.Results Agar colony formation assay showed that CAS inhibited growth of SW480 in a dose-dependent manner.The results of FCM analysis after PI staining showed that CAS induced apoptosis in SW480 cells in time-and concentration-dependent manner.Western Blotting analysis showed CAS up-regulated the expression of death receptor-5(DR5)and inhibition activity of nuclear factor kappaB(NF-κB).Conclusion CAS can inhibit the proliferation and induce apoptosis of human colon cancer SW480 cells in vitro and this action was associated with up-regulation of the expretion of the death receptor-5(DR5)and inhibition of NF-κB activity.

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Objective To observe the effect of casticin(CAS)on the growth and apoptosis of human colon cancer SW480 cells.Methods Human colon cancer SW480 cells were cultured in vitro.The capability of anchoring dependent growth in SW480 cells was determined using agar colony formation assay.Flow cytometry(FCM)analysis after PI staining and(FCM)was used to examine apoptosis rate in SW480 cells.Western Blotting was used to analyze the expression of DR5 and NF-κB(p65)protein.Results Agar colony formation assay showed that CAS inhibited growth of SW480 in a dose-dependent manner.The results of FCM analysis after PI staining showed that CAS induced apoptosis in SW480 cells in time-and concentration-dependent manner.Western Blotting analysis showed CAS up-regulated the expression of death receptor-5(DR5)and inhibition activity of nuclear factor kappaB(NF-κB).Conclusion CAS can inhibit the proliferation and induce apoptosis of human colon cancer SW480 cells in vitro and this action was associated with up-regulation of the expretion of the death receptor-5(DR5)and inhibition of NF-κB activity.

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Available abstract

Objective To observe the effect of casticin(CAS)on the growth and apoptosis of human colon cancer SW480 cells.Methods Human colon cancer SW480 cells were cultured in vitro.The capability of anchoring dependent growth in SW480 cells was determined using agar colony formation assay.Flow cytometry(FCM)analysis after PI staining and(FCM)was used to examine apoptosis rate in SW480 cells.Western Blotting was used to analyze the expression of DR5 and NF-κB(p65)protein.Results Agar colony formation assay showed that CAS inhibited growth of SW480 in a dose-dependent manner.The results of FCM analysis after PI staining showed that CAS induced apoptosis in SW480 cells in time-and concentration-dependent manner.Western Blotting analysis showed CAS up-regulated the expression of death receptor-5(DR5)and inhibition activity of nuclear factor kappaB(NF-κB).Conclusion CAS can inhibit the proliferation and induce apoptosis of human colon cancer SW480 cells in vitro and this action was associated with up-regulation of the expretion of the death receptor-5(DR5)and inhibition of NF-κB activity.

Key concepts: Apoptosis, Flow cytometry, Blot, Cell culture, Colorectal cancer, In vitro, Growth inhibition, Molecular biology

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