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
机构地区:[1]同济大学附属第十人民医院消化内科,上海200072
出 处:《同济大学学报(医学版)》2008年第3期79-83,共5页Journal of Tongji University(Medical Science)
基 金:上海市卫生局青年科研基金资助项目(20064650)
摘 要:目的胃癌是世界上最为常见的恶性肿瘤之一,预后较差,是人类主要的肿瘤致死病因。本研究旨在探讨转化生长因子β受体Ⅰ、Ⅱ(TβRⅠ、Ⅱ)和Smad 4 mRNA与胃癌发生、发展的关系。方法采用免疫组织化学和分子原位杂交的方法对67例胃癌、24例正常胃粘膜的TGFβ1蛋白和Smad 4 mRNA表达进行检测。结果胃癌组织中TβRⅠ、Ⅱ蛋白和Smad 4 mRNA表达率(分别为73.13%、49.25%和44.78%)较正常黏膜(均为95.83%)相比,均明显减弱(P<0.05)。TβRⅠ蛋白的表达与胃癌的临床病理因素无关(P>0.05),TβRⅡ蛋白和Smad 4 mRNA在胃癌中表达的变化与胃癌的临床病理因素有关(P<0.05)。TβRⅡ蛋白和Smad 4 mRNA在胃癌中表达的变化呈明显的负相关(P<0.05)。结论TβRⅡ蛋白和Smad 4 mRNA的低表达对细胞的恶性转化及增殖有一定的生物学意义。Objective Gastric cancer, the major cause of carcinoma death, is one of the most common malignant tumors in the world, which has a very poor prognosis. To evaluate the significance of transforming growth factor βreceptor ( TβR Ⅰ , Ⅱ ) protein and Smad 4 mRNA in pathogenisis and development of gastric cancer. Methods The TβR Ⅰ, Ⅱ protein and Smad 4 mRNA were detected respectively by immunohistochemistry and hybridization in situ (cDNA-mRNA) in 67 gastric cancer tissues and 24 normal gastric mucosa. Results About TβR Ⅰ, Ⅱ protein and Smad 4 mRNA, there was a significantly lower positive rate in gastric carcinoma(73.13% ,49.25% and 44.78% ,respectively) than that in normal gastric mucosa ( they are all 95.83% ), ( P 〈 0.05 ). Expression of TβR Ⅱ protein and Smad 4 mRNA in gastric cancer tissues show a strong relationship with the, but there shows no relationship between expression of TβR Ⅰ protein and clinicopathologocal factors. There exist a negative correlation of the positive expression between TβR Ⅱ and Smad 4 ( P 〈 0.05). Conclusion TβR Ⅱ protein and Smad 4 mRNA are involved in the gastric carcinoma cells proliferation and malignant transformation.
关 键 词:胃肿瘤 转化生长因子β受体Ⅰ 转化生长因子β受体Ⅱ SMAD4MRNA 免疫组织化学 原位杂交
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:216.73.216.49