hMLH1和hMSH2蛋白表达在遗传性非息肉病性大肠癌诊断中的应用  被引量:6

Detection of hMLH1/hMSH2 expression for identifying patients with hereditary nonpolyposis colorectal carcinoma

在线阅读下载全文

作  者:蔡三军[1] 徐烨[1] 陆洪芬[2] 蔡琦[2] 莫善兢[1] 孙孟红[2] 管祖庆[1] 施达仁[2] 

机构地区:[1]复旦大学附属肿瘤医院腹部外科,上海200032 [2]复旦大学附属肿瘤医院病理科,上海200032

出  处:《中华消化杂志》2004年第3期143-146,共4页Chinese Journal of Digestion

摘  要:目的 评价错配修复基因hMLH1和hMSH2蛋白表达在筛选遗传性非息肉病性大肠癌(HNPCC)中的价值。方法 收集大肠癌患者 6 6例 ,分为HNPCC患者 (A组 ,n =19)、高度可疑HNPCC患者 (B组 ,n =2 0 )、符合Bethesda指导标准的可疑HNPCC患者 (C组 ,n =14 )及散发性大肠癌患者 (D组 ,n =13)四组 ,用免疫组化方法检测各组错配修复基因hMLH1和hMSH2的蛋白表达。结果 A组hMLH1和hMSH2蛋白表达减低或缺失达 72 .8% ;B组为 6 0 .0 % ;C组为 2 8.4 % ;D组为 7.7%。hMLH1和hMSH2蛋白表达减低或缺失与HNPCC显著相关 (P =0 .0 0 0 8)。此外 ,hMLH1蛋白表达减低或缺失率显著高于hMSH2 (P <0 .0 1)。结论 hMLH1和hMSH2蛋白表达减低或缺失与HNPCC的可能性显著相关 ,免疫组化检测此二种蛋白表达能快速、有效地帮助临床医生评估患者HNPCC的可能性 ,同时提示相应错配修复基因存在突变。中国HNPCC患者中hMLH1基因发生突变的机会可能高于hMSH2基因。Objective To evaluate the significance of expression of hMLH1 and hMSH2 in detecting hereditary nonpolyposis colorectal carcinoma (HNPCC). Methods Colorectal carcinomas from 66 patients were examined by immunohistochemistry for the expressions of hMLH1 and hMSH2 using commercially available monoclonal antibodies. Immunohistochemical patterns of tumors from 19 HNPCC patients (Group A), 20 suspected HNPCC patients (Group B), 14 patients whose clinical features conformed to the Bethesda guideline (Group C), and 13 sporadic colorectal cancer patients (Group D) were compared. Results The absence or low expression of hMLH1 and hMSH2 was revealed in 72.8% patients of group A, 60.0% in group B, 28.4% in group C and 7.7% in group D. The absence or low protein expression of hMLH1 and hMSH2 was significantly correlated with HNPCC (P=0.0008). The absence or low expression of hMLH1 was higher detection rate than that hMSH2 (P=0.01). Conclusions HNPCC patients can be identified by immunohistochemical methods according to the expression of hMLH1 and hMSH2, which may be used in clinical practice and research. Immunohistochemical analysis of hMLH1 and hMSH2 may predict the presence of corresponding gene mutations. Gene mutation in hMLH1 might be higher than that in hMSH2 in Chinese HNPCC.

关 键 词:HMLH1蛋白 HMSH2蛋白 遗传性非息肉病性大肠癌 诊断 免疫组织化学 错配修复基因 

分 类 号:R735.34[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