hMSH2蛋白和P53蛋白表达在胃癌发病中的意义  被引量:2

Significance of gene product expressions of hMSH2 and P53 in gastric carcinogenesis

在线阅读下载全文

作  者:刘飞飞[1] 李梅[1] 王朝晖[1] 吕申[1] 

机构地区:[1]大连医科大学第二临床学院实验中心,辽宁大连116027

出  处:《大连医科大学学报》2006年第4期286-287,298,共3页Journal of Dalian Medical University

基  金:中国科学院知识创新工程领域前沿基金项目"国人胃癌遗传背景的研究"(No.DICPkaaaabc)的一分支

摘  要:[目的]探讨DNA错配修复基因hMSH2蛋白、抑癌基因P53蛋白表达在胃癌发病中的意义。[方法]采用免疫组织化学技术(S-P法)检测63例胃癌组织及32例胃炎组织hMSH2、P53的表达。[结果]胃癌组hMSH2蛋白阳性表达率(79.37%)明显高于胃炎组(53.13%)(P<0.05);胃癌组P53蛋白阳性表达率(88.89%)明显高于胃炎组(21.88%)(P<0.05)。hMSH2蛋白在高中分化腺癌、低分化腺癌及黏液癌的阳性表达率分别为73.68%、82.76%和80.00%,P53蛋白阳性表达率分别为100.00%、89.66%和73.33%,两者阳性表达率与胃癌分化程度均无显著性差异(P>0.05)。hMSH2蛋白和P53蛋白表达呈正相关。[结论]DNA错配修复基因hMSH2蛋白及抑癌基因P53蛋白的异常表达可能参与胃癌发生机制。[ Objective] To study the relationship of expressions of gene product hMSH2, P53 to gastric carcinogenesis. [ Method] Immunohistochemical technique was used to detect hMSH2 and P53 protein expressions in 63 cases of gastric carcinomas and 32 cases of gastritis. [ Results] The positive rate of hMSH2 in gastric carcinoma being 79.37 % (50/63) was significantly higher than that in gastritis being 53.13% (17/32) ( P 〈 0.05) ; the positive rate of P53 in gastric carcinoma being 88.89% (56/63) was significantly higher than that in gastritis being 21.88%(7/32) ( P 〈 0.05). The positive rates of hMSH2 in well medial differentiation, poor differentiation and mucoid carcinoma were 73.68%, 82.76% and 80.00% respectively( P 〉 0.05), and the positive rates of P53 were 100.00%, 89.66% and 73.33% respectively(P 〉 0.05). The expression of hMSH2 was positively correlated to the expression of P53 in gastric mucosa including carcinoma and gastritis ( r = 0.223, P 〈 0.05). [ Conclusion] The abnormal expressions of mismatch repair gene hMSH2 and tumor suppressor gene P53 may play some roles in the gastric carcinogenesis.

关 键 词:错配修复基因 HMSH2 抑癌基因 p53 胃癌 

分 类 号:R735.2[医药卫生—肿瘤]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象