reprimo基因启动子异常甲基化频率与吸烟习惯以及年龄相关;
14 3 3 σ启动子 异常甲基化与年龄、吸烟习惯、性别、病理类型和临床分期以及淋巴结转移等无 相关。结论nsclc中存在reprimo和14 3 3 σ等基因启动子较高频率的异常甲基化。
【关键词】 肺癌;甲基化;reprimo基因;14 3 3 σ基因 detection of aberrant methylation of reprimo and 14 3 3 σ genes in non small cell lung cancer jiang rui,yu shi ying cancer center of tongji hospital, tongji medical college, huazhong science and technology university, wuhan 430030, china corresponding author: yu shi ying, e mail: syyu@tjh.tjmu.edu.cn abstract:objective to investigate the frequency of aberrant methylation of reprimo and 14 3 3 σ in non small cell lung cancer (nsclc).methodsaberrant methylation of reprimo and 14 3 3 σ were examined by methylation specific pcr (msp) in primary nsclc and normal lung tissues (n = 60).resultsaberrant methylation of reprimo and 14 3 3 σ were found to be present in 36.67% and 28.33% of all nsclc patients respectively.three cases of aberrant methylation of reprimo(5%) and 4 cases of 14 3 3 σ(6.67%) were detected in normal lung tissues. the frequencies of aberrant methylation of reprimo and 14 3 3 σ between primary nsclc and normal lung tissue group were significantly different. aberrant methylation of reprimo was more frequently observed in older patients group (p=0.047) and smoking group (p=0.038). there was no significant correlation between reprimo methylation frequencies and sex, pathology type, clinical staging and lymphatic metastasis. similarly no significant association was found between 14 3 3 σ methylation frequencies and sex, age, pathology type, clinical staging, smoking habit and lymphatic metastasis.conclusionmethylation of reprimo and 14 3 3 σ may play an important role in the pathogenesis of nsclc. key words:lung cancer;
methylation;
reprimo;
14 3 3 σ tab 1primer sequence of reprimo and 14 3 3σgeneforward primerreverseprimerproduct14 3 3σmtggtagtttttatgaaaggcgtccctctaaccgcccaccacg105bp14 3 3σuatggtagtttttatgaaaggtgttccctctaaccacccaccaca107bpreprimomgcgagtgagcgtttagttcta cctaaaaccgaattcatcg112bpreprimouttgtgagtgagtgtttagtttgtaattacctaaaaccaaattcatc112bp 1资料与方法 1.1资料 1.1.1病理标本60例nsclc组织以及相应的癌旁无瘤肺组织标本来自华中科 技大学附属同济医院2005~2006年肺癌手术切除患者,组织经短时福尔马林固定 后取材,放入-20℃冰箱保存备用。Www.133229.cOm肿瘤组织采集时避开肿瘤 的液化坏死部分,对应的癌旁无瘤组织标本取材自距离肿瘤组织5cm以上的正常 肺组织。60例患者术前均未进行放、化疗。其中男41例,女19例,年龄34~73岁, 平均年龄53.6岁。肿瘤组织均经过病理学证实。按who标准分类,鳞癌32例,腺 癌28例。ⅰ期15例,ⅱ期26例,ⅲ期19例。淋巴结转移22例,未发生淋巴结转移 38例。
1.1.2试剂盒和试剂dna提取试剂盒以及50bp dna ladder marker购自tiangan 公司,dna 修饰试剂盒购自chemicon 公司,dna 聚合酶购自大连宝生物takara公 司,sssⅰ甲基转移酶购自美国neb公司。
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