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作 者:李华川[1] 陆士新[1] 崔晓邢 郭永军[1] 冯骆
机构地区:[1]中国医学科学院肿瘤研究所
出 处:《中华肿瘤杂志》1995年第4期249-253,共5页Chinese Journal of Oncology
基 金:国家"八.五"科技攻关资助课题
摘 要:为了研究人原发性食管癌组织中多种抑癌基因突变谱与甲基苄基亚硝胺(NMBzA)引起的人和猴食管上皮细胞中多种抑癌基因突变谱的相关性。我们应用PCR扩增与直接测序技术分析了人原发性食管癌和NMBzA处理的人和猴食管上皮细胞中多种抑癌基因p53,Rb,APC和MCC的突变谱;发现40.9%(9/22)的人原发性食管癌p53基因突变与NMBzA处理的人和猴食管上皮细胞中p53基因的突变相同,也发现NMBzA引起的人和猴食管上皮细胞中多种抑癌基因Rb、APC、MCC的突变谱与部分人原发性食管癌多种抑癌基因突变谱相同。首次从分子水平证明:NMBzA引起的多种抑癌基因突变谱与人原发性食管癌的突变谱有相关性,从而验证了NMBzA是我国食管癌的致病因子之一。Abstract The correlation between mutation spectra of tumor suppressor genes Rb,p53,APC andMCC in human esophageal cancer(EC) and in human and monkey esophageal epithelium treated withN-Methyl-N-Benzyl nitrosamine(NMBzA ) was studied using PCR amplification and direct sequenc-ing methods. The results showed that in 40.9%(9/22 ) of the specimen examined , the mutationspectrum of p53 in primary EC was similar to that in the esophageal epithelium of human fetus(in vit-ro)and monkey(in vivo ) treated with NMBzA. The same mutational spectra of tumor suppressorgenes Rb , APC , MCC in esophageal epithelium cells of human and monkey treated with NMBzAwere also found in some human primary EC. The correlation observed in the mutation spectra of mul-tiple tumor suppressor genes between human primary EC and the esophageal epithelia of human andmonkey origin treated with NMBzA wouldsuggest that NMBzA may be the esophageal etiological a-gent for human esophageal cancer in China.
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