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首页> 外文期刊>World Journal of Gastroenterology >Refinement of heterozygosity loss on chromosome 5p15 in sporadic colorectal cancer
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Refinement of heterozygosity loss on chromosome 5p15 in sporadic colorectal cancer

机译:散发性结直肠癌5p15染色体杂合性缺失的改善

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摘要

AIM: To refine the loss of heterozygosity on chromosome 5p15 and to identify the new tumor suppressor gene (s) in colorectal tumorigenesis. METHODS: Sixteen polymorphic microsatellite markers were analyzed on chromosome 5 and another 6 markers were applied on chromosome 5p15 in 83 cases of colorectal and normal DNA by PCR. PCR products were electrophoresed on an ABI 377 DNA sequencer. Genescan 3.1 and Genotype 2.1 software were used for LOH scanning and analysis. RESULTS: We observed 2 distinct regions of frequent allelic deletions on Chromosome 5, at D5S416 on 5p15 and D5S428-D5S410 on 5q. Another 6 polymorphric microsatellite markers were applied to 5p15 and the minimal region of frequent loss of heterozygosity was established on 5p15 spanning the D5S416 locus. CONCLUSION: Through our detailed deletion mapping studies, we have found a critical and precise location of 5p deletions, 5p15.2-5p15.3, which must contain one or more unknown tumor suppressor gene (s) of colorectal cancer.
机译:目的:改善5p15染色体上杂合性的丧失,并在结直肠肿瘤发生中鉴定新的抑癌基因。方法:采用PCR技术对83例结直肠和正常DNA患者的5号染色体进行了16种多态性微卫星标记分析,并对5p15染色体应用了另外6种标记。 PCR产物在ABI 377 DNA测序仪上电泳。使用Genescan 3.1和Genotype 2.1软件进行LOH扫描和分析。结果:我们在5p15的D5S416和5q的D5S428-D5S410上观察到了5号染色体上等位基因频繁缺失的2个不同区域。将另外6个多态微卫星标记应用于5p15,并在跨越D5S416基因座的5p15上建立了杂合性频繁丢失的最小区域。结论:通过详细的缺失作图研究,我们找到了5p缺失的关键和精确位置,即5p15.2-5p15.3,其中必须包含一个或多个未知的结直肠癌抑癌基因。

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