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加味四君子汤含药血清对胃癌细胞SGC-7901凋亡相关因子表达的影响
引用本文:聂闪闪,李洵,赵玉航,王东生. 加味四君子汤含药血清对胃癌细胞SGC-7901凋亡相关因子表达的影响[J]. 中国实验方剂学杂志, 2019, 25(9): 25-30
作者姓名:聂闪闪  李洵  赵玉航  王东生
作者单位:中南大学 湘雅医院, 长沙 410008,中南大学 湘雅医院, 长沙 410008,中南大学 湘雅医院, 长沙 410008,中南大学 湘雅医院, 长沙 410008
基金项目:国家自然科学基金项目(81373554);湖南省科技计划项目(2016SK2018)
摘    要:目的:研究加味四君子汤含药血清对胃癌细胞SGC-7901凋亡相关因子表达的影响,进一步探讨其具体抗肿瘤作用机制。方法:40只SD大鼠随机分为加味四君子汤低、中、高剂量组(0.213,0.426,0.853 g·kg~(-1)),空白组,每组10只,空白组给予等体积的生理盐水灌胃,各组连续灌胃10 d,末次给药1.5 h后,水合氯醛腹腔麻醉,心脏采血,分离血清,56℃灭菌,0.22μm过滤,制备加味四君子汤高、中、低剂量组含药血清,各剂量组含药血清孵育胃癌细胞SGC-7901,运用流式细胞仪检测细胞早期和晚期凋亡情况,运用实时荧光定量聚合酶链式反应(Real-time PCR)技术检测肿瘤抑制基因p53,c-核蛋白类基因(c-Myc),半胱氨酸天冬氨酸蛋白酶-3(Caspase-3),凋亡相关基因B细胞淋巴瘤-2(Bcl-2)mRNA的表达,运用细胞免疫荧光技术检测p53,c-Myc,Caspase-3,Bcl-2蛋白的相对表达量情况。结果:与空白组比较,加味四君子汤含药血清高剂量组细胞凋亡比率显著升高(P0.01),且可使胃癌细胞SGC-7901早期+晚期凋亡率达到22.58%(P0.01)。Real-time PCR结果显示加味四君子汤中剂量组能显著促进Caspase-3 mRNA表达(P0.01),加味四君子汤高剂量组能显著上调p53及c-Myc mRNA表达量(P0.01),加味四君子汤高剂量组显著抑制Bcl-2 mRNA表达(P0.01)。免疫荧光结果显示加味加味四君子汤高剂量组能使c-Myc,Caspase-3,p53蛋白表达水平显著升高(P0.01),而Bcl-2蛋白表达水平显著降低(P0.05)。结论:加味四君子汤含药血清能抑制抗凋亡蛋白Bcl-2的表达,促进凋亡相关分子p53,c-Myc,Caspase-3的表达,发挥抗肿瘤作用。

关 键 词:加味四君子汤含药血清  胃癌细胞SGC-7901  细胞凋亡  肿瘤抑制基因p53  c-核蛋白类基因(c-Myc)  半胱氨酸天冬氨酸蛋白酶-3(Caspase-3)  凋亡相关基因B细胞淋巴瘤-2(Bcl-2)
收稿时间:2018-08-23

Effect of Modified Si Junzitang Drug Serum on Expression of Apoptosis-related Molecules of Gastric Cancer Cell SGC-7901
NIE Shan-shan,LI Xun,ZHAO Yu-hang and WANG Dong-sheng. Effect of Modified Si Junzitang Drug Serum on Expression of Apoptosis-related Molecules of Gastric Cancer Cell SGC-7901[J]. China Journal of Experimental Traditional Medical Formulae, 2019, 25(9): 25-30
Authors:NIE Shan-shan  LI Xun  ZHAO Yu-hang  WANG Dong-sheng
Affiliation:Xiangya Hospital, Central South University, Changsha 410008, China,Xiangya Hospital, Central South University, Changsha 410008, China,Xiangya Hospital, Central South University, Changsha 410008, China and Xiangya Hospital, Central South University, Changsha 410008, China
Abstract:Objective: To explore the effect of modified Si Junzitang (MSJZT) drug serum on the expression of apoptosis-related molecules of gastric cancer cell SGC-7901 and further its anti-tumor mechanism.Method: A total of 40 SD rats were randomly divided into four groups:low-dose,middle-dose,high-dose MSJZT (0.213,0.426,0.853 g·kg-1) groups and normal group (n=10).The treatment groups were administrated through gastric perfusion,and the normal group was given the equivalent volume of normal saline for 10 days.1.5 h after the last treatment,chloral hydrate peritoneal anesthesia was performed,blood was collected from heart,and different doses of serum were separated to prepare drug-containing serum of low-dose,middle-dose,high-dose MSJZT groups,in order to incubate SGC-7901 gastric cancer cell.Early and late apoptosis rates were detected with flow cytometry.Afterwards,the tumor suppressor gene p53,c-nucleoprotein gene (c-Myc),cysteine-aspartic acid protease-3(Caspase-3),B-cell lymphoma-2(Bcl-2) mRNA expressions were confirmed by fluorescence quantitative polymerase chain reaction (Real-time PCR).The protein expressions of p53,c-Myc,Caspase-3,Bcl-2 were detected by immunofluorescence.Result: Compared with the normal group,the high-dose MSJZT group could obviously increase the apoptosis rate to 22.58%(P<0.01).The results of Real-time PCR showed that the middle-dose MSJZT group significantly promoted the mRNA expression of Caspase-3(P<0.01),the medium-dose group significantly increased the mRNA expressions of p53 and c-Myc (P<0.01),and the high-dose group significantly inhibited the mRNA expression of Bcl-2(P<0.01).The immunofluorescence results showed that the high-dose MSJZT group could significantly increase the protein expressions of c-Myc,Caspase-3 and p53(P<0.01),while the protein expression of Bcl-2 was significantly reduced (P<0.05).Conclusion: MSJZT drug serum could exert an anti-tumor effect by inhibiting the expression of the anti-apoptotic protein Bcl-2,and promoting the expressions of pro-apoptotic-related molecules p53,c-Myc,Caspase-3.
Keywords:modified Si Junzitang (MSJZT) drug serum  gastric cancer SGC-7901  apoptosis  tumor suppressor gene p53 (p53)  c-nucleoprotein gene (c-Myc)  cysteine-aspartic acid protease-3 (Caspase-3)  B-cell lymphoma-2 (Bcl-2)
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