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首页> 外文期刊>British Journal of Cancer >Absence of somatic alterations of the EB1 gene adenomatous polyposis coli-associated protein in human sporadic colorectal cancers
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Absence of somatic alterations of the EB1 gene adenomatous polyposis coli-associated protein in human sporadic colorectal cancers

机译:散发性结直肠癌中EB1基因腺瘤性息肉病相关蛋白的体细胞改变

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摘要

The human EB1 gene product was recently found, by a yeast two-hybrid screening, to be associated with the carboxy terminus of the APC (adenomatous polyposis coli) protein, the product of a tumour-suppressor gene thought to act as a gatekeeper in colorectal carcinogenesis. Because virtually all of the APC mutations result in the synthesis of carboxy-terminal truncated proteins, mutant APC proteins are expected to lose their ability to interact with EB1 gene product. Thus, the interaction between APC and EB1 proteins may be important for the tumour-suppressor activity of APC protein, and raises the hypothesis that EB1 is also involved in sporadic colorectal tumorigenesis. To investigate this hypothesis, somatic mutations in the entire coding sequence of EB1 cDNA were searched by reverse transcriptase single-strand conformational polymorphism (SSCP) analysis in 21 sporadic colorectal cancers and seven adenomas. None of these tumours contained somatic mutation, whereas a silent cDNA variant was identified in 14% of alleles. Furthermore, to investigate whether EB1 locus was included within a region subjected to losses of heterozygosity, four polymorphism markers surrounding EB1 locus were surveyed. Only one out of 28 colorectal tumours contained a loss of heterozygosity at the D20S107 marker. In conclusion, the present findings strongly suggest that EB1 gene is not involved in somatic colorectal carcinogenesis.
机译:最近,通过酵母双杂交筛选发现了人EB1基因产物与APC(腺瘤性息肉病)蛋白的羧基末端有关,APC蛋白是一种肿瘤抑制基因的产物,被认为在结直肠中起着守门员的作用。致癌作用。因为实际上所有的APC突变都会导致羧基末端截短蛋白的合成,所以突变的APC蛋白有望失去与EB1基因产物相互作用的能力。因此,APC和EB1蛋白之间的相互作用对于APC蛋白的肿瘤抑制活性可能很重要,并提出了EB1也参与散发性结直肠肿瘤发生的假设。为了研究该假设,通过逆转录酶单链构象多态性(SSCP)分析在21例散发性结直肠癌和7例腺瘤中搜索了EB1 cDNA整个编码序列中的体细胞突变。这些肿瘤均不包含体细胞突变,而在14%的等位基因中发现了沉默的cDNA变异。此外,为了调查在杂合性丧失的区域中是否包括EB1基因座,对EB1基因座周围的四个多态性标记物进行了调查。 28个大肠肿瘤中只有1个在D20S107标记处杂合性丧失。总之,本研究结果强烈提示EB1基因不参与体细胞结直肠癌的发生。

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