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:戴凌[1] 谭宁[2] 田小林[1] 温海滨[3] 黄岚珍[2]
机构地区:[1]桂林医学院附属医院普通外科,541001 [2]桂林医学院生物科学实验中心,541001 [3]广西壮族自治区河池市人民医院肾内科
出 处:《中国医药》2012年第7期870-872,共3页China Medicine
基 金:科技部癌基因及相关基因国家重点实验室开放课题
摘 要:目的探讨细胞外基质金属蛋白酶诱导因子(EMMPRIN)基因对小鼠结肠癌细胞CT26侵袭的影响。方法构建包含EMMPRIN基因编码框的真核表达载体pCMV-HA2-EMMPRIN,通过脂质体转染CT26细胞,经G418筛选,建立稳定表达EMMPRIN基因的CT26细胞株。对照组为CT26小鼠结肠癌细胞,EMMPRIN组为转染EMMPRIN的小鼠结肠癌细胞。通过体外侵袭实验,分析EMMPRINCT26细胞侵袭力的改变。通过蛋白质印迹、酶联免疫吸附测定及明胶酶谱实验分析过表达EMMPRIN,CT26细胞基质金属蛋白酶2(MMP-2)合成、分泌、激活的变化。结果当EMMPRIN基因在CT26细胞稳定过表达后,侵袭实验的结果为EMMPRIN组(98±5)个细胞,对照组(48±6)个细胞(P〈0.01)。蛋白质印迹、酶联免疫吸附测定及明胶酶谱实验结果证实,EMMPRIN可明显促进CT26细胞MMP-2的分泌及激活,但对CT26细胞MMP-2的合成无影响。结论EMMPRIN基因可明显促进小鼠结肠癌细胞CT26的侵袭,并可明显促进CT26细胞MMP-2的分泌及激活。Objective To investigate whether extracellular matrix metalloproteinase inducer(EMMPRIN) can enhance the metastatic ability of murine colon adenocarcinoma cell(CT26). Methods EMMPRIN was over-ex- pressed in CT26 cells through transfecting pCMV-HA2-EMMPRIN into the CT26 ceils. Invasion assay was utihzed to analyze the invasion of CT26 cells in vitro after EMMPRIN over-expression. The synthesis of matrix metalloprotein- ase-2 (MMP-2) and the secreted and activated MMP-2 were examined by western blot, Enzyme linked immunosor- bent assay(ELISA) and zymography. Results After EMMPRIN over-expression,invasion assay showed that inva- sive cells were 98±5 in EMMPRIN group and 48±6 in control group ( P 〈 0.01 ). The secreted and activated MMP-2 was up-regulated in EMMPRIN group cell culture media, but the synthesis of MMP-2 was no different be- tween EMMPRIN group and control group. Conclusions Over-expression of EMMPRIN can enhance the CT26 cell invasion and up-regulate the secreted and activated MMP-2 in CT26 cells. The results suggest that EMMPRIN may be involved in cancer metastasis and play an important role in promotion of cancer metastasis.
关 键 词:细胞外基质金属蛋白酶诱导因子 结肠癌细胞 转移
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:216.73.216.217