2011China Journal of Chinese OphthalmologyRequires access

Effects of matrine on the growth and proliferation of retinoblastoma cells

Lun Fang

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Abstract

OBJECTIVE To study the effect of matrine on the apoptosis of retinoblastoma cells.METHODS Retinoblastoma cells were cultured in 0.4 mmol/L matrine for 12 hours,24 hours or 48 hours respectively,and the control group was cultured in equivalence of the standard the nutrient solution RPMI-1640 at concentrations of 10% fatal bovine serum substitute for matrine.The apoptosis rate was evaluated by flow cytometry.RESULTS Apoptotic cells were observed after 12 h,and then developed in a time-dependent manner after 48 hours.The difference was statistically significant compared with the control group(P0.05).Followed by 12 h of matrine treatment,the ratio of viable apoptotic cells to total ones was 89.20%,and then decreased to 78.97% and 76.12% by 24 h and 48 h respectively.CONDLUSIONS Matrine could inhibit the proliferation of retinoblastoma cells though induction of its apoptosis in time-dependent manner.

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OBJECTIVE To study the effect of matrine on the apoptosis of retinoblastoma cells.METHODS Retinoblastoma cells were cultured in 0.4 mmol/L matrine for 12 hours,24 hours or 48 hours respectively,and the control group was cultured in equivalence of the standard the nutrient solution RPMI-1640 at concentrations of 10% fatal bovine serum substitute for matrine.The apoptosis rate was evaluated by flow cytometry.RESULTS Apoptotic cells were observed after 12 h,and then developed in a time-dependent manner after 48 hours.The difference was statistically significant compared with the control group(P0.05).Followed by 12 h of matrine treatment,the ratio of viable apoptotic cells to total ones was 89.20%,and then decreased to 78.97% and 76.12% by 24 h and 48 h respectively.CONDLUSIONS Matrine could inhibit the proliferation of retinoblastoma cells though induction of its apoptosis in time-dependent manner.

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Available abstract

OBJECTIVE To study the effect of matrine on the apoptosis of retinoblastoma cells.METHODS Retinoblastoma cells were cultured in 0.4 mmol/L matrine for 12 hours,24 hours or 48 hours respectively,and the control group was cultured in equivalence of the standard the nutrient solution RPMI-1640 at concentrations of 10% fatal bovine serum substitute for matrine.The apoptosis rate was evaluated by flow cytometry.RESULTS Apoptotic cells were observed after 12 h,and then developed in a time-dependent manner after 48 hours.The difference was statistically significant compared with the control group(P0.05).Followed by 12 h of matrine treatment,the ratio of viable apoptotic cells to total ones was 89.20%,and then decreased to 78.97% and 76.12% by 24 h and 48 h respectively.CONDLUSIONS Matrine could inhibit the proliferation of retinoblastoma cells though induction of its apoptosis in time-dependent manner.

Key concepts: Matrine, Retinoblastoma, Apoptosis, Flow cytometry, Medicine, Andrology, Significant difference, Molecular biology

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