首页|丹参酮ⅡA对胃癌BGC-823细胞增殖及凋亡的影响

丹参酮ⅡA对胃癌BGC-823细胞增殖及凋亡的影响

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目的 以胃癌BGC-823细胞为研究对象,观察不同浓度丹参酮ⅡA对胃癌BGC-823细胞活力的影响,探讨丹参酮ⅡA促BGC-823细胞凋亡机制。方法 取对数生长期的BGC-823细胞,分别加入0。5、1。0、2。0、5。0 mg/L浓度丹参酮ⅡA培养12 h。光学显微镜观察BGC-823细胞形态学变化,MTT实验检测丹参酮ⅡA对细胞活力的影响,流式细胞术检测细胞凋亡率,Western blot实验检测凋亡相关蛋白BcL-2,Bax和Cleaved-Caspase-3的表达。结果 光学显微镜观察发现,不同浓度丹参酮ⅡA均可导致细胞形态发生改变;MTT实验显示,丹参酮ⅡA作用于BGC-823细胞12h后,明显降低细胞活力,并且存在剂量依赖性(P<0。05或P<0。01);流式细胞术检测结果显示,丹参酮ⅡA对BGC-823细胞作用12 h后各浓度组早期凋亡比例分别为(5。80±0。32)%(P<0。05)、(7。90±0。43)%(P<0。05)、(10。20±0。42)%(P<0。01)、(20。44±1。24)%(P<0。01);Western blot实验检测结果显示,不同浓度丹参酮ⅡA作用细胞12 h后,与对照组相比,丹参酮ⅡA实验组BGC-823细胞Bax和Cleaved-Caspase-3蛋白表达水平呈上调趋势,Bcl-2蛋白表达水平呈下调趋势。结论 丹参酮ⅡA抑制BGC-823细胞活力并促进凋亡,且具有剂量依赖性。
Effect of Tanshinone ⅡA on Viability and Apoptosis of Human Gastric Cancer BGC-823 Cells
Objective In this study,the effects of different concentrations of tanshinone ⅡA on the viability of gastric cancer BGC-823 cells were observed,and the mechanism of tanshinone ⅡA promoting the apoptosis of BGC-823 cells was investigated. Methods BGC-823 cells at logarithmic growth stage were cultured with 0.5,1.0,2.0 and 5.0 mg/L tanshinone ⅡA,respectively,for 12 hours.The mor-phological changes of BGC-823 cells were observed by optical microscope,and the inhibitory effect of tanshinone ⅡA on cell viability was detected by MTT assay. Flow cytometry was used to detect apoptosis rate. The expressions of apoptosis-related proteins Bcl-2,Bax and Cleaved-Caspase-3 were detected by Western blot. Results Light microscopy showed that different concentrations of tanshinone ⅡA could lead to changes in cell morphology. The MTT assay demonstrated a significant inhibition of BGC-823 cell viability following 12-hour treatment with tanshinone ⅡA in a dose-dependent manner(P<0.05 or P<0.01).Flow cytometry demonstrated that following a 12-hour treatment of tanshinone ⅡA on BGC-823 cells,the proportions of early apoptosis in each concentration group were(5.80±0.32)%(P<0.05),(7.90±0.43)%(P<0.05),(10.20±0.42)%(P<0.01),and(20.44±1.24)%(P<0.01),respectively. The results of the Western blot assay demonstrated that following the treatment of BGC-823 cells with various concentrations of tanshinone ⅡA for a duration of 12 hours,there was a tendency for the expression levels of Bax and Cleaved Caspase-3 protein in the experimental group to be up-regulated,in comparison to the control group. Similarly,the expression levels of Bcl-2 protein appeared to be down-regulated. Conclusions Tan-shinone ⅡA inhibits BGC-823 cell viability and promotes apoptosis in a dose-dependent manner.

tanshinone ⅡAcell viabilitycell apoptosisBGC-823 cells

杜婧雯、何奇、丁思嫄、王馨、方贵海、张巍

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吉林医药学院 临床医学院,吉林 吉林 132013

吉林医药学院 公共卫生学院,吉林 吉林 132013

北华大学 基础医学院,吉林 吉林 132013

吉林医药学院 基础医学院,吉林 吉林 132013

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丹参酮ⅡA 细胞活力 细胞凋亡 BGC-823细胞

吉林省科技厅科技发展项目吉林省教育厅"十三五"科学技术研究项目吉林医药学院2022年度大学生创新创业训练计划项目

20190701062GHJJKH20200453KJX202213706003

2024

吉林医药学院学报
吉林医药学院

吉林医药学院学报

影响因子:0.459
ISSN:1673-2995
年,卷(期):2024.45(5)