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Effects of curcumin on proliferation and apoptosis of human ovarian cancer cell lineHO-8910 in vitro

Tang Gui-xia

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Abstract

Objective:To investigate the regulatory effects of curcumin on proliferation and apoptosis of human ovarian cancer cell line HO-8910 in vitro. Methods:Human ovarian cancer cell line HO-8910,cultured in vitro,was treated with 1.25-20 μg/ml curcumin for 6~24 h. Morphological changes of cells were observed with invert microscope, and growth inhibition rates of HO-8910 cells were measured with MTT method. The cell cycle distribution and apoptosis were detected by flow cytometic analysis. In addition, the expression of Fas,Fas-L,Bcl-2 and Bax in HO-8910 cell was observed by SABC immunohistochemistry. Results: Curcumin inhibited the proliferation of HO-8910 cells in a dose-and time-dependent manner. The cell growth was arrested at S and G2/M stage and aneuploid peak was observed by FCM. The expression of Fas,Fas-L,Bcl-2 was increased while the expression of Bax was both positive before and after treatment. Conclusion:The curcumin not only inhibits proliferation but also induces apoptosis of human ovarian cancer cell line HO-8910.

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Objective:To investigate the regulatory effects of curcumin on proliferation and apoptosis of human ovarian cancer cell line HO-8910 in vitro. Methods:Human ovarian cancer cell line HO-8910,cultured in vitro,was treated with 1.25-20 μg/ml curcumin for 6~24 h. Morphological changes of cells were observed with invert microscope, and growth inhibition rates of HO-8910 cells were measured with MTT method. The cell cycle distribution and apoptosis were detected by flow cytometic analysis. In addition, the expression of Fas,Fas-L,Bcl-2 and Bax in HO-8910 cell was observed by SABC immunohistochemistry. Results: Curcumin inhibited the proliferation of HO-8910 cells in a dose-and time-dependent manner. The cell growth was arrested at S and G2/M stage and aneuploid peak was observed by FCM. The expression of Fas,Fas-L,Bcl-2 was increased while the expression of Bax was both positive before and after treatment. Conclusion:The curcumin not only inhibits proliferation but also induces apoptosis of human ovarian cancer cell line HO-8910.

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Available abstract

Objective:To investigate the regulatory effects of curcumin on proliferation and apoptosis of human ovarian cancer cell line HO-8910 in vitro. Methods:Human ovarian cancer cell line HO-8910,cultured in vitro,was treated with 1.25-20 μg/ml curcumin for 6~24 h. Morphological changes of cells were observed with invert microscope, and growth inhibition rates of HO-8910 cells were measured with MTT method. The cell cycle distribution and apoptosis were detected by flow cytometic analysis. In addition, the expression of Fas,Fas-L,Bcl-2 and Bax in HO-8910 cell was observed by SABC immunohistochemistry. Results: Curcumin inhibited the proliferation of HO-8910 cells in a dose-and time-dependent manner. The cell growth was arrested at S and G2/M stage and aneuploid peak was observed by FCM. The expression of Fas,Fas-L,Bcl-2 was increased while the expression of Bax was both positive before and after treatment. Conclusion:The curcumin not only inhibits proliferation but also induces apoptosis of human ovarian cancer cell line HO-8910.

Key concepts: Curcumin, Apoptosis, Cell growth, Cell culture, In vitro, Cell, Biology, Cancer research

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