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首页> 外文期刊>British Journal of Cancer >Variants of the long control region and the E6 oncogene in European human papillomavirus type 16 isolates: implications for cervical disease
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Variants of the long control region and the E6 oncogene in European human papillomavirus type 16 isolates: implications for cervical disease

机译:欧洲人乳头瘤病毒16型分离株中长控制区和E6癌基因的变异:对宫颈疾病的影响

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High-risk human papillomavirus types, especially type 16, are risk factors for cervical cancer. Preliminary studies suggest that HPV16 polymorphisms in the long control region or in the E6 gene may alter the oncogenic potential of the virus. This could partially explain why some lesions progress to cancer while others do not. A systematic study combining the long control region and E6 has not been undertaken. This prompted us to investigate the long control region and the E6 in northern European women infected with human papillomavirus 16. We identified the sequence variations of both regions and investigated the long control region promoter activity among various isolates. In addition, we correlated the distribution of long control region and E6 polymorphisms with disease status. We analyzed 45 samples from Swedish and Finnish women. The long control region and the E6 gene were sequenced after polymerase chain reaction long control region fragments of six European isolates covering the majority of polymorphisms in this region were ligated into the pALuc vector and used for luciferase assays. In European HPV16 isolates, polymorphisms in the long control region are more frequent than in the E6 gene. Nevertheless, the promoter function was slightly increased in only one of the tested European long control region variants. In addition, we found a specific European E6 variant, L83V, to be enriched in high-grade lesions and cancer rather than a specific European long control region variant. The difference in oncogenicity between European HPV16 genotypes is more probably due to an altered property of the corresponding E6 proteins rather than to an altered activity of the P97 promoter.
机译:高危型人乳头瘤病毒类型,尤其是16型是宫颈癌的危险因素。初步研究表明,长控制区或E6基因中的HPV16多态性可能会改变病毒的致癌潜能。这可以部分解释为什么某些病变发展为癌症而另一些则没有。尚未进行结合长控制区和E6的系统研究。这促使我们调查感染了人乳头瘤病毒16的北欧妇女的长控制区和E6。我们鉴定了这两个区域的序列变异,并调查了各种分离株之间的长控制区启动子活性。此外,我们将长控制区的分布和E6多态性与疾病状况相关联。我们分析了瑞典和芬兰女性的45个样本。在聚合酶链反应后对长控制区和E6基因进行测序,将覆盖该区域大部分多态性的六个欧洲分离株的长控制区片段连接到pALuc载体中,用于荧光素酶测定。在欧洲HPV16分离株中,长控制区的多态性比E6基因中的多。然而,启动子功能仅在测试的欧洲长控制区变体之一中略有增加。此外,我们发现特定的欧洲E6变体L83V可以富含高级别病变和癌症,而不是特定的欧洲长控制区变体。欧洲HPV16基因型之间致癌性的差异很可能是由于相应的E6蛋白的特性发生了变化,而不是由于P97启动子的活性发生了变化。

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