青藤碱联合氟尿嘧啶对人胃腺癌SGC7901细胞增殖及凋亡的影响 |
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引用本文: | 周溯. 青藤碱联合氟尿嘧啶对人胃腺癌SGC7901细胞增殖及凋亡的影响[J]. 蚌埠医学院学报, 2015, 40(8): 998-1001. DOI: 10.13898/j.cnki.issn.1000-2200.2015.08.004 |
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作者姓名: | 周溯 |
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作者单位: | 四川石油总医院 药剂科, 四川 成都 610213 |
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摘 要: | 目的:探讨青藤碱联合氟尿嘧啶(5-Fu)对人胃癌SGC7901细胞增殖及Bcl-2、Bax和环氧化酶(COX)-2表达的影响。方法:体外培养人胃腺癌SGC7901细胞系,四甲基偶氮唑蓝法测定对照组、5-Fu组(5-Fu 50 mg/L)、青藤碱低浓度组(青藤碱 1.25 mmol/L)、青藤碱中浓度组(青藤碱2.5 mmol/L)、青藤碱高浓度组(青藤碱 5 mmol/L)及联合组(5-Fu 25 mg/L+青藤碱2.5 mmol/L)对SGC7901细胞增殖作用的影响;碘化丙啶染色流式细胞术检测细胞周期变化及凋亡率;免疫细胞化学法测定Bcl-2、Bax和COX-2蛋白表达情况。结果:青藤碱、5-Fu作用SGC7901细胞24、48和72 h后,青藤碱对人胃腺癌SGC7901细胞的增殖具有抑制作用,呈时间、浓度依赖性,与5-Fu联用后协同抑制细胞增殖(P<0.05~P<0.01);5-Fu组、青藤碱各浓度组及联合组的细胞凋亡率均较对照组明显增高(P<0.01),其中联合组均较单药组的凋亡率明显降低(P<0.01)。对照组Bcl-2和COX-2蛋白表达较明显,而青藤碱组、5-Fu组及其联合组染色减弱;与对照组差异均有统计学意义(P<0.05~P<0.01),其中联合组均较单药组阳性率明显降低(P<0.01)。对照组Bax蛋白表达较弱,青藤碱组、5-Fu组及其联合组阳性率相对增加;与对照组比较差异均有统计学意义(P<0.01),且联合组均较单药组阳性率明显升高(P<0.01)。结论:青藤碱联合5-Fu对人胃腺癌SGC7901细胞增殖具有协同抑制作用,能够上调Bax表达,下调Bcl-2、COX-2表达,可能发挥增敏作用。
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关 键 词: | 胃肿瘤 青藤碱 氟尿嘧啶 细胞增殖 凋亡 |
收稿时间: | 2014-03-31 |
The effects of sinomenine combined with 5-fluomuracil on the proliferation and apoptosis in human gastric gland carcinoma cell line SGC 7901 |
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Affiliation: | Department of Pharmacy, General Hospital of Sichuan Petroleum Bureau, Chengdu Sichuan 610213, China |
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Abstract: | Objective:To explore the effects of sinomenine combined with 5-fluomuracil(5-Fu) on the proliferation of human gastric gland carcinoma cell line SGC 7901 and expressions of Bcl-2,Bax and COX-2. Methods:The human gastric gland carcinoma cell line SGC 7901 was cultured in vitro,which was divided into the control group,5-Fu group(50 mg/L),low concentration sinomenine group (1.25 mmol/L),medium concentration sinomenine group(2. 5 mmol/L),high concentration sinomenine group(5 mmol/L) and combination group(25 mg/L of 5-Fu and 2. 5 mmol/L of sinomenine). The proliferation of SGC7901 cells was detected by MTT,the cell cycle and apoptosis rate were determined by flow cytometry, and the expressions of Bcl-2, Bax and COX-2 were detected by immunohistochemistry. Results:Sinomenine could inhibit the proliferation of SGC7901 cells after 24 h,48 h and 72 h of treatment, which was dose- and time-dependent, and the treatment with sinomenine combined with 5-Fu could strengthen the inhibitory effects (P<0. 05 to P<0. 01). Compared with the control group,the apoptosis rates in 5-Fu group,sinomenine groups and combination group increased obviously(P<0. 01),and the apoptosis rate in combination group was significantly lower than that in single drug group(P<0. 05 to P <0. 01). The positive expressions of Bcl-2 and COX-2 in the control group,and the sinomenine group,5-Fu group and combination group were strong and weak,respectively,the differences of whose were statistical significance(P<0. 05 to P<0. 01). The positive rates of Bcl-2 and COX-2 expressions in combination group were lower than those in single drug group(P<0. 01 ). The positive expression of Bax in the control group,and the sinomenine group,5-Fu group and combination group were weak and strong,respectively, the differences of whose were statistically significant(P<0. 01). The positive rate of Bax expression in combination group was higher than that in single drug group(P<0. 01). Conclusions:Sinomenine combined with 5-Fu can enhance the inhibitory effect on SGC7901 cells proliferation,which can further upregulate the expression of Bax,and downregulate the expressions of Bcl-2 and COX-2 protein. |
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Keywords: | stomach neoplasms sinomenine 5-fluomuracil cell proliferation apoptosis |
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