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机构地区:[1]惠州市第一人民医院消化内科,广东惠州516001
出 处:《医学综述》2015年第21期3969-3971,共3页Medical Recapitulate
基 金:广东省医学科研究课题(B2011340)
摘 要:目的采用聚合酶链反应-单链构象多态性(PCR-SSCP)银染法检测腺瘤多发性息肉病(APC)、p53、K-ras三个基因在结直肠肿瘤筛查中的敏感性和特异性。方法选择2011年11月至2012年8月惠州市第一人民医院消化门诊收治的14例结直肠癌(CRC组),60例结直肠腺瘤(CRA组),30例正常组粪便标本,提取DNA,PCR-SSCP银染法检测基因突变。结果 APC、p53、K-ras三个基因联合检测在CRC组、CRA组、正常组突变率分别为57.1%(8/14)、30.0%(18/60)、3.3%(1/30);在结直肠肿瘤的灵敏度和特异度分别为35.1%(26/74)、96.7%(29/30),粪便DNA联合检测CRC组、CRA组的检出率高于正常组(均P<0.05)。结论粪便DNA联合检测在无创性筛查结直肠肿瘤中具有可行性,可能是一种适合于结直肠肿瘤筛查的无创性方法和筛查模式。Objective To detect the sensitivity and specificity of gene adenomatous polyposis (APC) , p.53, K-ras genetic mutations in colorectal neoplasm using the ploymerase chain reaction-single-strand confer- mational polymorphism(PCR-SSCP) silver staining. Methods Samples were enrolled from individuals who came to Huizhou First People's Hospital Gastroenterology Clinic from Nov. 2011 to Aug. 2012:14 cases of colorectal cancer( CRC group) ,60 cases of coloroctal adenomas( CRA group) ,30 cases of normal stool speci- mens, DNA was extrated, PCR-SSCP silver staining was used to detect genetic mutations. Results The mutation rates of three genes APC, p.53, K-ras detection in CRC, CRA and normal group were 57.1% (8/ 14) ,30. 0% (18/60) and 3.3% (1/30) respectively. The sensitivity and specificity of three genes detection coloroctal neoplasm were 35.1% (26/74)and 96. 7% (29/30). The detection rate of three genes in CRC and CRA group were significantly higher than normal group( all P 〈 0. 05 ). Conclusion Stool DNA detec- tion is a feasibi]e non-invasive method for screening colorectal neoplasm, which might he a suitable non-inva- sive method for screening colorectal neoplasia.
关 键 词:结直肠肿瘤 粪便DNA 聚合酶链反应-单链构象多态性 腺瘤多发性息肉病基因 p53 K-RAS
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