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:陈陵[1] 王宗华[2] 宋航[1] 黄一[1] 王国威[1] 王仙园[2] 任辉[2]
机构地区:[1]解放军第324医院消化内科,重庆400020 [2]解放军第三军医大学护理学院
出 处:《中华实验外科杂志》2014年第3期474-476,共3页Chinese Journal of Experimental Surgery
基 金:国家自然科学基金资助项目(30900679);重庆市自然科学基金资助项目(cstc2011jjA10111)
摘 要:目的 观察微小RNA(miR)-29a对人胃癌SGC-7901细胞裸鼠皮下移植瘤生长的影响.方法 以磷酸盐缓冲液(PBS)为空白对照,以负载cel-miR67的复制缺陷型腺病毒(Ad-cel)为阴性对照,注射负载miR-29a的复制缺陷型腺病毒(Ad-miR29a)液于移植瘤内,观察移植瘤生长曲线和抑瘤率;采用实时定量逆转录聚合酶链反应(RT-qPCR)检测移植瘤内miR-29a表达丰度;采用免疫组织化学技术检测CD34表达以计算移植瘤内微血管密度(MVD).结果 与PBS组比较,Ad-miR29a组移植瘤内miR-29a表达显著上调(3.06±0.73比1.00±0.21,P<0.01),而Ad-cel组与PBS组比较差异无统计学意义(P>0.05);Ad-miR29a组移植瘤生长速度低于PBS组,而Ad-cel组与PBS组差异无统计学意义(P>0.05);于第5周末Ad-miR29a组抑瘤率达49.30%;Ad-miR29a组的移植瘤内MVD显著低于PBS组(21.3±8.1比42.6±11.2,P<0.01),而Ad-cel组与PBS组比较差异无统计学意义(P>0.05).结论 miR-29a可显著抑制裸鼠胃癌移植瘤生长,其机制可能为抑制移植瘤内MVD,miR-29a有望成为新型的胃癌基因治疗靶标.Objective To study the effect of microRNA (miR)-29a on the growth of human gastric cancer cell line SGC-7901 xenografts in nude mice.Methods The SGC-7901 cell line was injected subcutaneously into nude mice to establish the model of human gastric cancer xenografts.The replicationdeficient recombinant adenovirus carrying miR-29a (Ad-miR29a) was injected into the xenografts.The phosphate buffered saline (PBS) solution was employed as blank control and the adenovirus carrying celmiR-67 (Ad-cel) as negative control.The growth curve of the tumor xenografts was observed and the inhibitory rate of tumor was calculated.The expression of miR-29a was detected using real-time reverse transcriptase-polymerase chain reaction (RT-qPCR).The microvessel density (MVD) was calculated by CD34 detection using immunohistochemistry in the xenografts.Results Comparing to the PBS group,the expression level of miR-29a of xenografts in the Ad-miR29a group was significantly up-regulated (3.06 ± 0.73 vs.1.00 ±0.21,P < 0.01),while no significant difference was detected between Ad-cel and PBS group.The growth of xenografts in the Ad-miR29a group was suppressed apparently comparing to the PBS group,while no significant change was detected between Ad-cel and PBS group.At the end of the 5th weekend,the tumor inhibition rate reached 49.30% in Ad-miR29a group.The MVD counts of xenografts in the Ad-miR29a group were down-regulated significantly comparing to that in PBS group (21.3 ± 8.1 vs.42.6 ± 11.2,P <0.01),while no significant change was detected between Ad-cel and PBS group.Conclusion The up-regulation of miR-29a can suppress the growth of gastric cancer xenografts in nude mice by inhibiting the MVD in tumors,which makes miR-29a a promising novel target for gene therapy for human gastric cancer.
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:3.148.240.165