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作 者:赵成海[1] 张宁[1] 卜献民[2] 李岩[3] 张海鹏[1]
机构地区:[1]中国医科大学病理生理教研室,辽宁省沈阳市110001 [2]中国医科大学附属二院普通外科,辽宁省沈阳市110004 [3]中国医科大学附属二院消化内科,辽宁省沈阳市110004
出 处:《世界华人消化杂志》2006年第10期1004-1007,共4页World Chinese Journal of Digestology
摘 要:目的:检测胃癌组织中p16,hMLH1,E-cadherin和RUNX3基因甲基化状态,探讨多基因甲基化在胃癌发病中的作用.方法:采用饱和氯化钠法提取肿瘤组织、瘤旁组织及正常胃黏膜组织DNA.采用甲基化特异PCR对上述基因甲基化状态进行分析.结果:在正常胃黏膜组织中,38.9%存在E-cadherin甲基化,16.7%存在RUNX3甲基化,没有发现p16和hMLH1甲基化;在癌旁组织中,p16、hMLH1、E-cadherin和RUNX3甲基化频率分别为8.3%,4.2%,54.2%和29.2%;在胃癌组织中,上述基因甲基化频率分别为33.3%,20.8%,0.8%和54.2%.66.7%胃癌被检出存在2个或2个以上基因甲基化,明显高于癌旁组织(37.5%,χ2=4.09,P<0.05)和正常胃黏膜组织(5.6%,χ2=15.94,P<0.01),而癌旁组织则高于正常胃黏膜组织(χ2=4.16,P<0.05).有5例胃癌没有检出任何一种基因甲基化.结论:多基因甲基化是部分胃癌发展过程中一种早期事件,提示多基因甲基化在这部分胃癌的发病中起重要作用.AIM: To determine the methylation status of p16, hMLH1, E-cadherin and RUNX3 genes in gastric cancer. METHODS: DNA in gastric cancer, canceradjacent tissues and normal gastric mucosa was extracted by saturated sodium chloride (NaCl) solution. The methylation status of p16, hMLH1, E-cadherin and RUNX3 genes were detected by methylation-specific polymerase chain reaction (MSP). RESULTS: Methylations of E-cadherin and RUNX3 were found in 38.9% and 16.7% normal gastric mucosa, respectively. Methylations of p16 and hMLH1 were not observed in any normal gastric mucosa. The frequencies of p16, hMLH1, E-cadherin and RUNX3 methylations were 8.3%, 4.2%, 54.2% and 29.2%, respectively,in cancer-adjacent tissues, and 33.3%, 20.8%, 70.8% and 54.2%, respectively, in gastric cancer. Methylations of two or more genes were found in 66.7% gastric cancer, which was significantly higher than that in cancer-adjacent tissues (37.5%, %2 = 4.09, P 〈 0.05) and normal gastric mucosa (5.6%, %2 = 15.94, P 〈 0.01). Methylations were also significantly different between cancer-adjacent tissues and normal gastric mucosa (%2 = 4.16, P 〈 0.05). None of the above gene mythylation was detected in 5 gastric cancer tissues. CONCLUSION: Multiple gene methylation is an early event in some gastric cancers and it plays an important role in the development of these gastric cancers.
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