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作 者:邓龙文[1] 江宁[1] 谭国林[1] 周鸣[1] 湛凤凰[1] 谢奕[1] 曹莉 李桂源[1]
机构地区:[1]湖南医科大学肿瘤研究所
出 处:《中华肿瘤杂志》1998年第4期248-250,共3页Chinese Journal of Oncology
基 金:国家863项目;自然科学基金
摘 要:目的细胞遗传学研究表明,3号染色体缺失是鼻咽癌常见的染色体异常之一。分子生物学研究表明,染色体3p在鼻咽癌中出现高频率的等位基因杂合性丢失(LOH)。本研究将进一步确定鼻咽癌3p等位基因杂合性丢失的频率及范围。方法应用位于3p2126区域16个微卫星多态性位点,对24例低分化鼻咽癌患者进行了LOH分析。结果24例患者中有16例存在杂合性丢失(66.7%)。丢失频率最高的两个位点是D3S1560(50%,11/21)和D3S1620(50%,9/18)。在具有丢失的16例患者中,8例显示为1个连续的多个相邻位点的杂合性丢失区域,5例患者存在2个或2个以上的杂合性丢失区。病例1,3,4,7,8,10,16,17,18,19和22在D3S1597和D3S1297之间,表现为一个不同大小的杂合性丢失区。结论最小共同丢失区位于D3S1560D3S1620(3p25.326.2)之间,提示该区域有一个尚未克隆的、与晚期鼻咽癌明显相关的抑癌基因。Objective To determine the frequency and extent of loss of heterozygosity (LOH) on chromosome 3p in nasopharyngeal carcinoma(NPC). Methods Sixteen loci on chromosome bands 3p21 26 in 24 tumors was studied by using microsatellite analysis. Results LOH on 3p21 26 was found in 16 of 24 tumors (66.7%). The highest frequency of the allelic loss was found in two adjacent loci D3S1620(50%, 11/22) and D3S1560 (50%, 9/18). Eight cases showed LOH in one contiguous region and 5 cases in more than one region. Sample 1, 3,4,7,8,10,16,17,18,19, and 22 had a contiguous stretch of allelic loss between D3S1297 and D3S1597. Conclusion The smallest common LOH/deletion region seems likely to lie between D3S1620(3p26.2 26.3) and D3S1560(3p25.3). The allelic loss map defined here will facilitate finer mapping of putative tumor suppressor gene loci and positional cloning of such genes, which may play a role in carcinogenesis of NPC.
分 类 号:R739.630.2[医药卫生—肿瘤]
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