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:张晓娜[1] 张学彦[2] 于旸[3] 乔虹[1] 胥景峰
机构地区:[1]哈尔滨医科大学第二附属医院内分泌科,黑龙江哈尔滨150086 [2]哈尔滨医科大学第二附属医院消化内科,黑龙江哈尔滨150086 [3]哈尔滨医科大学遗传学教研室,黑龙江哈尔滨150086
出 处:《现代生物医学进展》2015年第28期5432-5434,5483,共4页Progress in Modern Biomedicine
摘 要:目的:探讨NF-κB信号传导通路中转化生长因子激活激酶1(TAK1)靶点对胃癌AGS细胞系增殖的影响。方法:利用si RNA沉默胃癌AGS细胞系中的TAK1基因,通过Western Blot验证细胞中TAK1基因的沉默情况,双项荧光素酶报告基因系统检测TAK1基因沉默对AGS细胞系NF-κB信号传导通路活性的影响,软琼脂克隆形成实验检测沉默TAK1基因对胃癌AGS细胞系成瘤能力的影响,MTT法检测沉默TAK1基因对胃癌AGS细胞系增殖能力的影响。结果:与对照组Sis-Con细胞相比,TAK1基因沉默组Sir-TAK1-1/Sir-TAK1-2细胞中NF-κB信号传导通路活性明显受抑制;TAK1基因沉默组Sir-TAK1-1/Sir-TAK1-2细胞软琼脂克隆形成的集落数目明显减少,差异具有统计学意义(P<0.05),且细胞生长的速度明显减慢。结论:TAK1是NF-κB信号传导通路激活的关键因子,沉默TAK1基因可以抑制AGS胃癌细胞系的成瘤性和增殖力。Objective: To investigate the effect of transforming growth factor-activated kinase 1(TAK1) of NF- κB signaling pathway on the proliferation of AGS gastric cancer cell. Methods: TAK1 gene of AGS cells was silenced by si RNA and then confirmed by western blot. The effect of silencing TAK1 gene on the activity of NF-κB signaling pathway, cell tumorigenicity and cell proliferation were determined by dual-luciferase reporter gene system, soft agar clone formation assay and MTT assay, respectively. Results: The activity of NF- κB signaling pathway in Sir-TAK1-1/Sir-TAK1-2 cells was significantly inhibited after silencing TAK1 gene when compared with Sis-Con group cells. Moreover, the number of clone formation of Sir-TAK1-1/Sir-TAK1-2 cells was dramatically decreased, and significant differences were found compared with Sis-Con group cells(P〈0.05). The growth of Sir-TAK1-1/Sir-TAK1-2cells was significantly decreased. Conclusion: TAK1 gene is the key factor for activating NF-κB signaling pathway. The tumorigenicity and proliferation of AGS gastric cancer cell lines could be inhibited by silencing TAK1 gene.
关 键 词:转化生长因子激酶1(TAK1) NF-ΚB 胃癌
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:216.73.216.72