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作 者:邹明瑾[1] 高杨[1] 罗兵[2] 梁华[2] 李燕[1]
机构地区:[1]山东大学齐鲁医院检验科,山东济南250012 [2]青岛大学医学院分子病毒学实验室,山东青岛266012
出 处:《中国现代普通外科进展》2005年第6期352-354,共3页Chinese Journal of Current Advances in General Surgery
摘 要:目的:分析抑癌基因PTEN突变高发区外显子5(exon5)和外显子8(exon8)在胃癌组织中的突变频率,探讨其突变与胃癌临床分期的相关性。方法:应用聚合酶链反应-单链构像多态性分析(PCR-SSCP)方法检测胃癌组织和相应癌旁正常组织中PTEN基因的突变,对突变样本的PCR产物进行测序分析。结果:42例胃癌组织中检测到PTEN基因突变3例,突变率为7.14%(3/42);42例胃癌临床病理分期,Ⅰ、Ⅱ期突变率为5.88%(1/17),Ⅲ、Ⅳ期突变率为8.00%(2/25),二者差异无统计学意义(P〉0.05)。42例相应癌旁正常组织未检测到突变。42例胃癌进行组织学分级,低分化腺癌突变率为12.00%(3/25),中、高分化腺癌突变率为0(0/17),二者差异无统计学意义(P〉0.05)。结论:胃癌组织中存在PTEN基因突变,主要发生在低分化腺癌中,而PTEN基因突变与胃癌病理组织学分级和临床病理分期之间无明显相关性。Objective:TO study the mutation frequencies of the exon 5 and the exon 8 of PTEN (phosphatase and tensin homology deleted on chromosome ten) gene in gastric carcinoma and investigate the relationship of the gene mutation and pathological differentiation and clinical stage. Methods :The mutation of exon 5 and exon 8 of PTEN gene was detected in 42 gastric carcinoma samples and the matched adjacent normal gastric muoosa with polymerase chain reaction-single strand conformation polymorlahism(POR-SSOP) method, The PCR products of mutant samples were analysed by DNA sequencing technique. Results : The mutation of PTEN was shown in 3 of the 42 Bast.rio carclnoma tissues and in none of the adjacent normal tissues. The mutation rates of PTEN gene in poorly differentiated and well differentiated samcles were 12. 00% and 0, respectively (P〉0. 05). The mutation rates of PTIEN gene in clinical stage Ⅰ and Ⅱ (5.8896) had no significant difference with that in clinicat stage Ⅲ and Ⅳ (8. 00%) (P〉0. 05). Conclusion :PTEN gene mutation occurs mainly in poorly differentiated gastric carcinoma tissues, and the mutation rate is not relate'd to pathological differentiation and clinical stage.
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