大肠肿瘤p53和ki-ras基因协同突变的研究  被引量:2

Collaborative mutation of p53 and ki-ras genes in colorectal cancer

在线阅读下载全文

作  者:侯睿哲[1] 侯睿智[2] 彭云香[2] 侯治富[2] 

机构地区:[1]吉林大学白求恩医学院,吉林长春130021 [2]吉林大学中日联谊医院,吉林长春130033

出  处:《中国实验诊断学》2010年第6期917-919,共3页Chinese Journal of Laboratory Diagnosis

基  金:吉林省科技发展计划项目(200705391)资助;吉林大学"大学生创新性实验计划"项目(2009B71067)资助

摘  要:目的探讨大肠肿瘤p53和ki-ras基因协同突变的临床意义。方法采用免疫组化和PCR-SSCP方法,检测58例大肠肿瘤患者的良性病变、良性病变转为恶变、原发腺癌组织的p53基因、ki-ras基因的表达和突变情况。结果良性病变组与恶变组间的p53基因和Ki-ras基因的表达有显著差异,良性病变组与原发腺癌组的Ki-ras基因表达差异显著;良性病变组的p53基因与Ki-ras基因的表达呈负相关,而恶变组和原发腺癌组呈正相关。p53基因和ki-ras基因两种基因突变率无显著差异,而协同突变与淋巴结转移密切相关,相关系数r=0.335,P=0.017,P<0.05。结论 p53和ki-ras基因协同突变可以促进了大肠癌的发展。监测p53基因和Ki-ras基因的协同表达和突变,有助于大肠肿瘤的早期诊断和预后评价。Objective To explore p53 and ki:ras genes collaborative mutation in colorectal cancer patients.Methods The p53 gene and ki-ras gene expression and mutation were detected in 58 cases of colorectal cancer patients with benign lesions, benign lesions to malignant, primary adenocarcinoma by immunohistochemical staining and PCR-SSCP method respectively. Results The Expressions of P53 gene and Ki-ras gene were significantly different between benign group and malignant group. The Ki-ras gene expression of benign lesions and primary adenocarcinoma was significantly different. And in benign lesions, the expression of the 1953 gene and Ki-ras gene was negatively correlated, while the malignant group and the primary adenocarcinoma showed positive correlation. The mutations between 1:53 gene and ki-ras gene was no significant difference in a concerted mutation. Synergistic gene mutation of p53 gene and ki-ras gene is closely related to lymph node metastasis. R = 0.335, P = 0. 017, P 〈 0.05. Conclusion p53 and ki-ras gene mutation can contribute to the synergy of colorectal cancer development. Monitoring the P53 gene and Ki-ras gene expression and mutation of the synergy will help the early diagnosis and prognosis in colorectal cancer patients.

关 键 词:P53基因 KI-RAS基因 大肠肿瘤 协同突变 

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