检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:陈晓珩[1] 何蓓[2] 李会龙[1] 户蕊 李璐[1] 王鑫[1] 汪唐顺[1] 李乃卿[1] 丁治国[1]
机构地区:[1]北京中医药大学东直门医院外一科,北京101121 [2]北京中医药大学第三附属医院医务处,北京100029
出 处:《中国现代普通外科进展》2017年第6期421-425,共5页Chinese Journal of Current Advances in General Surgery
基 金:国家自然科学基金项目(81673972);北京中医药大学自主选题项目(2016-JYB-JSMS-030);北京市通州区卫生发展科研专项(TWKY-2016-PT-01-03)
摘 要:目的:研究参芪扶正注射液与干扰素α(IFN-α)联用时对肝癌细胞STAT1基因表达的影响,探讨其对IFN-α协同增效的作用机制。方法:运用MTT法检测IFN-α注射液单独或与参芪扶正注射液联合对MHCC97-L细胞增殖的影响;运用Real-time PCR和Western-blot分别检测IFN-α单独或与参芪扶正注射液联用对STAT1 RNA和蛋白质表达的影响;构建STAT1干扰慢病毒载体并实现其在MHCC97-L中表达,通过RT-PCR、We s te rn-Blot验证其干扰STAT1表达的有效性;MTT法检测IFN-α单独或联合参芪扶正注射液对STAT1基因"沉默"细胞株增殖的影响。结果 :与单独使用IFN-α相比,参芪扶正注射液与IFN-α联用可以增强IFN-α对人肝癌MHCC97-L的抑制作用(P<0.01),并上调STAT1 mRNA(P<0.05)和蛋白质的表达(P<0.05);成功构建STAT1基因"沉默"的MHCC97-L细胞株;参芪扶正注射液协同IFN-α对STAT1基因"沉默"MHCC97-L的抑制率与单独使用IFN-α差异无统计学意义(P>0.05)。结论:参芪扶正注射液可上调人肝癌细胞MHCC97-L中STAT1的表达,从而提高IFN-α的疗效。Objective: To study the effect of Shenqi Fuzheng injection combined with interfer- on- α (IFN- α) on the expression of STAT1 gene in hepatocellular carcinoma cells, and to elucidate its mechanism of IFN-α synergistic effect. Methords: The effect of IFN-a injection alone or combined with Shenqi Fuzheng injection on the proliferation of MHCC97-L cells was detected by MTT assay. IFN-α was detected by Real-time PCR and Western-blot respectively. The expression of STAT1 mRNA and protein in the experimental group, the negative control group (NaCI) and the blank control group were determined, and the effect of Shenqi Fuzheng injection on the transcription and expression of STAT1 was determined. The expression of STAT1 in lentiviral vector MTT assay was used to detect the effect of IFN- α alone or in combination with Shenqi Fuzheng injection on the STAT1 gene "silencing" cells. The expression of STAT1 was detected by RT-PCR and Western-Blot in MHCC97L cells. Strain, on cell proliferation. Results: Compared with IFN-α alone, Shenqi Fuzheng injection combined with IFN-α enhanced the inhibitory effect of IFN-α on MHCC97-L (P〈0.01) and up-regulated the expression of STATlmRNA and protein (P〈0.05). Successfully constructed the STAT1 gene "silent" in the MHCC97-L cell line, There was no significant difference in the inhibition rate of MHCC97-L between Shenqi Fuzheng injection and IFN-α(P〉0.05). Conclu. sion: Shenqi Fuzheng Injection can up-regulate the expression of STAT1 in human hepatocellular carcinoma cell line MHCC97-L, so as to increase the effect of IFN-α.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.79