首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >Polymorphisms in the p53 gene in thyroid tumours and blood samples of children from areas in Belarus.
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Polymorphisms in the p53 gene in thyroid tumours and blood samples of children from areas in Belarus.

机译:白俄罗斯地区儿童甲状腺癌和血液样本中p53基因的多态性。

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摘要

We present changes in the p53 gene in a group of 70 thyroid tumours and 40 blood samples obtained from children from Belarus. Three thyroid tumours show a polymorphism in exon 6 (codon 213) and 5 tumours show a polymorphism in intron 6, 37 bp upstream to the 5'-end of exon 7. Only one patient has a mutation in exon 7 (codon 258) resulting in an amino acid substitution in the protein p53. The distribution of polymorphisms in the 40 blood samples was as follows: three patients had a polymorphism in exon 6 and two persons had a polymorphism in intron 6. One polymorphism in intron 6 was also found in the group of 30 healthy children from Belarus. The fact that the differences in the sequence in p53 found in the tumours was also seen in the blood of these patients demonstrates that they are polymorphisms not induced by radiation exposure. It is difficult to conclude, if the polymorphisms found by us could be associated with the predisposition to radiation-induced cancer.
机译:我们介绍了一组70例甲状腺疾病和40例从白俄罗斯儿童那里获得的血液样本中p53基因的变化。 3例甲状腺肿瘤在6号外显子(第213号密码子)显示多态性,5例在内含子6中在第7号外显子5'端上游37 bp处显示多态性,只有一名患者的第7外显子发生突变(第258号密码子) p53蛋白中的氨基酸取代。 40个血液样本中的多态性分布如下:3例患者的6号外显子具有多态性,2例6号内含子具有多态性。在30名来自白俄罗斯的健康儿童中也发现6号内含子具有多态性。在这些患者的血液中也发现了在肿瘤中发现的p53序列差异的事实,表明它们是多态性,并非由辐射暴露引起。很难得出结论,我们发现的多态性是否可能与辐射诱发的癌症易感性有关。

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