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Loss of heterozygosity on hromosome 1 in sporadic colorectal carcinoma

机译:散发性结直肠癌中1号染色体杂合性的丧失

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AIM: Loss of heterozygosity (LOH) on tumor suppressor genes is believed to play a key role in carcinogenesis of colorectal cancer. When it occurs at a tumor suppressor gene locus with abnormal allele, neoplastic transformation happens. In this study, we analyzed the LOH at 21 loci on chromosome 1 in sporadic colorectal cancer to identify additional loci involved in colorectal tumorigenesis. METHODS: Twenty-one polymorphic micro-satellite DNA markers were analyzed with PCR both in 83 cases of colorectal cancer and in normal tissues. PCR products were eletrophoresed on an ABI 377 DNA sequencer. Genescan 3.1 and Genotype 2.1 software were used for LOH scanning and analysis. χ~2 test was used to compare LOH frequency with clinicopathological data. P<0.05 was considered as statistically significant. RESULTS: The average LOH frequency of chromosome 1, short arm and long arm was 19.83%, 18.00% and 21.66%, respectively. The 2 highest LOH loci with a frequency of 36.54% and 32.50% were identified on D1S468 (1p36.33-p36.31) and D1S413 (1q31.3), respectively. On D1S2726 locus, LOH frequency of rectal cancer was 28.57% (6/21), which was higher than that of colon cancer (0.00%, 0/33) (P=0.002), suggesting that the mechanism of carcinogenisis was different in both groups. CONCLUSION: Putative tumor suppressor genes on chromosome 1 may relate to sporadic colorectal carcinomas. Tumor-suppressor-genes might locate on 1p36.33-36.31 and/or 1q31.3.
机译:目的:肿瘤抑制基因的杂合性丧失(LOH)被认为在结直肠癌的致癌作用中起着关键作用。当它出现在具有异常等位基因的肿瘤抑制基因位点时,就会发生肿瘤转化。在这项研究中,我们分析了散发性结直肠癌中1号染色体上21个基因座的LOH,以鉴定参与结直肠癌发生的其他基因座。方法:采用PCR技术对83例大肠癌和正常组织中的21个多态性微卫星DNA标记进行了分析。 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。采用χ〜2检验比较LOH频率与临床病理数据。 P <0.05被认为具有统计学意义。结果:染色体1,短臂和长臂的平均LOH频率分别为19.83%,18.00%和21.66%。在D1S468(1p36.33-p36.31)和D1S413(1q31.3)上分别识别出频率最高的2个LOH基因座,频率分别为36.54%和32.50%。在D1S2726位点,直肠癌的LOH频率为28.57%(6/21),高于结肠癌的LOH频率(0.00%,0/33)(P = 0.002),这表明两者的致癌机制不同组。结论:1号染色体上的抑癌基因可能与散发性结直肠癌有关。肿瘤抑制基因可能位于1p36.33-36.31和/或1q31.3。

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