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作 者:顾昊[1,2] 王海波[1] 冯俊[1] 钱亚云[1] 金凤[1] 陈珏[1] 史有阳 陆松花 徐佩[1] 刘延庆[1]
机构地区:[1]扬州大学医学院,江苏扬州225009 [2]南京脑科医院,南京210009
出 处:《中国实验方剂学杂志》2017年第17期115-120,共6页Chinese Journal of Experimental Traditional Medical Formulae
基 金:国家自然科学基金项目(81274141;81450051;81403232;81573656);江苏省自然科学基金项目(BK20141280);江苏省中医药科技项目(LZ11210);江苏省普通高校研究生科研创新项目(KYZZ_0370)
摘 要:目的:探讨南蛇藤茎乙酸乙酯提取物(Celastrus orbiculatus extract,COE)抗人胶质母细胞瘤U251细胞株的增殖和凋亡作用,研究COE抗肿瘤的分子机制,为寻找新的治疗胶质母细胞瘤药物提供依据。方法:以人胶质母细胞瘤细胞株U251为研究对象,设空白组和COE组,应用噻唑蓝[3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2-H-tetrazolium bromide,MTT]比色法观察COE对细胞活力的抑制作用;5-溴脱氧尿嘧啶核苷(5-bromo-2-deoxy uridine,Brd U)标记检测COE对U251细胞增殖的影响;Annexin V/碘化丙啶(PI)双标法检测COE对U251细胞凋亡的作用;透射电镜下观察经COE干预后U251细胞超微结构变化;蛋白免疫印迹法(Western blot)检测COE对凋亡标志基因B淋巴细胞瘤-2(B-cell lymphoma-2,Bcl-2),Bcl-2相关X蛋白(Bcl-2-associated X,Bax)和半胱氨酸蛋白酶-3(Caspase-3)蛋白表达的影响。结果:与空白组比较,COE能够明显抑制U251细胞的增殖(P<0.05);诱导U251细胞的早期凋亡,电镜下可见到凋亡小体,影响并改变U251细胞超微结构;COE能促进Caspase-3,Bax蛋白表达,降低Bcl-2,Bcl-2/Bax蛋白表达(P<0.05)。结论:COE能有效抑制胶质母细胞瘤U251细胞株的增殖,促进肿瘤细胞凋亡,其作用机制与调节Bcl-2和Caspase-3表达有关。Objective: To observe the effect of different concentrations of Celastrus orbiculatus extract (COE) on proliferation and apoptosis of U251 cells (a glioblastoma cancer cell line), and its possible molecular mechanism. Method: U251 cells at the logarithmic growth phase were divided into control group and COE-treated group. 3- (4, 5-dimethyl-2-thiazolyl) -2, 5-diphenyl-2-H-tetrazolium bromide (MTT) assay and 5-bromo-2- deoxy uridine (BrdU) incorporation experiment were performed to observe the ~nhibitory effect on cell viability and proliferation, respectively. Annexin V/PI double staining was used to detect the effect of COE on U251 cell apoptosis. Uhrastructural changes of U251 cells after COE treatment were observed under transmission electron microscope; the protein expressions of apoptosis marker B-cell lymphoma-2/Bcl-2-associated X (Bcl-2/Bax) and Caspase-3 were detected by Western blot. Result: Compared to control group, the proliferation of U251 cells in COE-treated group were significant inhibited by COE (P 〈 0.05). COE could induce the early apoptosis and uhrastructure changes of U251 cells, and apoptotic bodies were observed under transmission electron microscope. The protein expressions of Bcl-2/Bax and Caspase-3 were changed in a concentration dependent manner. Conclusion: COE can effectively inhibit the proliferation of U251 cells by down-regulating the expression of Bcl-2/ Bax and increasing the protein expression of Caspase-3, and promoting the apoptosis of cell, suggesting that COE can be used as a drug candidate for treating glioblastoma.
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