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鼻咽癌染色体11q13等位基因杂合性缺失的研究
引用本文:郭颖,方女燕,黄必军,梁启万,郝亚萍,曾益新. 鼻咽癌染色体11q13等位基因杂合性缺失的研究[J]. 中华肿瘤杂志, 2001, 23(2): 132-134
作者姓名:郭颖  方女燕  黄必军  梁启万  郝亚萍  曾益新
作者单位:中山医科大学肿瘤防治中心肿瘤研究所
基金项目:美国CMB基金资助项目(98-678);国家杰出青年科学基金(B类)资助项目(39825511)、广东省自然科学基金重大项目(980950,98001-4);中山医科大学“211工程”重点学科建设资助项目(98045)
摘    要:目的:对鼻咽癌中染色体11q13上的4个位点进行微卫星多态性分析,明确这些位点染色体位基因杂合性丢失的情况。方法:采用显微切割的方法获取较纯的肿瘤组织,然后用PCR的方法以PYGM、D11S4946、D11S449和INT-2为引物,对38例鼻咽癌进行微卫生序列分析。结果38例鼻咽癌组织中,至少有一个位点出现杂合性缺失者36例,占94.7%。其中D11S4946杂合性缺失的频率最高,占78.8%(26/33),其余的引物分别为:INT-2占51.5%(17/33),PYGM占45.5%(15/33),D11S449占45.7%(16/35)。结论鼻咽癌染色体11q13区发生高频率杂合性缺失,提示缺失区域可能存在与鼻咽癌发生有关的抑癌基因。

关 键 词:鼻咽肿瘤 染色体11q13 杂合性缺失 鼻咽癌
修稿时间:1999-10-20

Study of loss of heterozygosity at chromosome 11q13 in nas opharyngeal carcinoma
Y Guo,Y Fang,B Huang. Study of loss of heterozygosity at chromosome 11q13 in nas opharyngeal carcinoma[J]. Chinese Journal of Oncology, 2001, 23(2): 132-134
Authors:Y Guo  Y Fang  B Huang
Affiliation:Department of Etiology, Cancer Center, Sun Yat-sen University of Medical Sciences, Guangzhou 510060, China.
Abstract:OBJECTIVE: To analyze the loss of heterozygosity (LOH) from STS sites at 11q13 in nasopharyngeal carcinoma(NPC). METHODS: Relatively pure tumor tissues were obtained by microdissetion. PCR was used to perform microsatellite analysis of NPC samples using D11S4946, PYGM, D11S449 and INT-2 as primers, which span the MEN-1 gene. RESULTS: Thirty-six of 38 cases studied showed LOH in at least one of the loci analyzed. Among the primers used, D11S4946 had the highest frequency of LOH, (78.8%). The LOH frequency was 51.5% for INT-2, 45.5% for PYGM and 45.7% for D11S449, respectively. CONCLUSION: The high frequency of loss of heterozygosity at 11q13 in NPC implies that there may be some tumor suppressor gene(s) involved in NPC tumorigenesis.
Keywords:Nasopharyngeal neoplasms  Chromosome 11q13  Loss of heterozygosity
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