2009Chongqing Yike Daxue xuebaoRequires access

Effects of all-trans retinoic acid on the human ovarian cancer HO8910 cell line

Zhao Chun-quan

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Abstract

Objective:To investigate the effects of all-trans retinoic acid on the human ovarian cancer cell line HO8910.Methods:The human ovarian cancer cell line HO8910 cultured in vitro were treated with various concentrations of all-trans retinoic acid.The cell proliferation inhibition was detected by MTT assay;The morphologic changes of cell differentiation were observed under inverted microscope;The invasion capability was evaluated by transwell chambers.Results:1.ATRA of 10-7~10-5mol/L inhibited the proliferation of HO8910 cell significantly in a dose-dependent and time-dependent manner(P0.05)and its IC50 were 2.331×10-5 mol/L、0.998×10-6 mol/L、0.891×10-7 mol/L at 24 hours、48 hours and 72 hours,separately.2.Treated by 10-6 mol/L ATRA,HO8910 cells showed striking morphological characteristics of differentiation under microscope.3.The number of invasive cells decreased significantly after treated by 10-6 mol/L ATRA(P0.05).Conclusion:ATRA can both inhibit the proliferation and invasion of human ovarian cancer cell line HO8910,Which expect to provide an effective and novel approach for clinical treatment of human ovarian cancer.

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Objective:To investigate the effects of all-trans retinoic acid on the human ovarian cancer cell line HO8910.Methods:The human ovarian cancer cell line HO8910 cultured in vitro were treated with various concentrations of all-trans retinoic acid.The cell proliferation inhibition was detected by MTT assay;The morphologic changes of cell differentiation were observed under inverted microscope;The invasion capability was evaluated by transwell chambers.Results:1.ATRA of 10-7~10-5mol/L inhibited the proliferation of HO8910 cell significantly in a dose-dependent and time-dependent manner(P0.05)and its IC50 were 2.331×10-5 mol/L、0.998×10-6 mol/L、0.891×10-7 mol/L at 24 hours、48 hours and 72 hours,separately.2.Treated by 10-6 mol/L ATRA,HO8910 cells showed striking morphological characteristics of differentiation under microscope.3.The number of invasive cells decreased significantly after treated by 10-6 mol/L ATRA(P0.05).Conclusion:ATRA can both inhibit the proliferation and invasion of human ovarian cancer cell line HO8910,Which expect to provide an effective and novel approach for clinical treatment of human ovarian cancer.

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Available abstract

Objective:To investigate the effects of all-trans retinoic acid on the human ovarian cancer cell line HO8910.Methods:The human ovarian cancer cell line HO8910 cultured in vitro were treated with various concentrations of all-trans retinoic acid.The cell proliferation inhibition was detected by MTT assay;The morphologic changes of cell differentiation were observed under inverted microscope;The invasion capability was evaluated by transwell chambers.Results:1.ATRA of 10-7~10-5mol/L inhibited the proliferation of HO8910 cell significantly in a dose-dependent and time-dependent manner(P0.05)and its IC50 were 2.331×10-5 mol/L、0.998×10-6 mol/L、0.891×10-7 mol/L at 24 hours、48 hours and 72 hours,separately.2.Treated by 10-6 mol/L ATRA,HO8910 cells showed striking morphological characteristics of differentiation under microscope.3.The number of invasive cells decreased significantly after treated by 10-6 mol/L ATRA(P0.05).Conclusion:ATRA can both inhibit the proliferation and invasion of human ovarian cancer cell line HO8910,Which expect to provide an effective and novel approach for clinical treatment of human ovarian cancer.

Key concepts: Retinoic acid, Ovarian cancer, Cell culture, Cell, Cell growth, In vitro, Cancer cell, Cancer research

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