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首页> 外文期刊>Cancer Medicine >Methylation of CpG 5962 in L1 of the human papillomavirus 16 genome as a potential predictive marker for viral persistence: A prospective large cohort study using cervical swab samples
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Methylation of CpG 5962 in L1 of the human papillomavirus 16 genome as a potential predictive marker for viral persistence: A prospective large cohort study using cervical swab samples

机译:人乳头瘤病毒16基因组中CpG 5962的甲基化作为病毒持久性的潜在预测标志物:使用宫颈拭子样品的前瞻性大队列研究

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Several studies have demonstrated that the viral genome can be methylated by the host cell during progression from persistent infection to cervical cancer. The aim of this study was to investigate whether methylation at a specific site could predict the development of viral persistence and whether viral load shows a correlation with specific methylation patterns. HPV16‐positive samples from women aged 20–29?years (n?=?99) with a follow‐up time of 13?years, were included from a Danish cohort comprising 11?088 women. Viral load was measured by real‐time PCR and methylation status was determined for 39 CpG sites in the upstream regulatory region (URR), E6/E7, and L1 region of HPV16 by next‐generation sequencing. Participants were divided into two groups according to whether they were persistently (≥?24?months) or transiently HPV16 infected. The general methylation status was significantly different between women with a persistent and women with a transient infection outcome (P?=?.025). One site located in L1 (nt.?5962) was statistically significantly (P?=?.00048) different in the methylation status after correction using the Holm‐Sidak method (alpha?=?0.05). Correlation analyses of samples from HPV16 persistently infected women suggest that methylation is higher although viral load is lower. This study indicates that methylation at position 5962 of the HPV16 genome within the L1 gene might be a predictive marker for the development of a persistent HPV16 infection.
机译:几项研究表明,在从持续感染到宫颈癌的进展期间,宿主细胞可以甲基化病毒基因组。本研究的目的是研究特定部位的甲基化是否可以预测病毒持久性的发展,以及病毒载是否显示与特定甲基化模式的相关性。来自20-29岁的女性的HPV16阳性样本?年后续时间为13岁的岁月(n?=?99),包括在丹麦队列中包括11个?088名女性。通过实时PCR测量病毒载量,通过下一代测序测定HPV16的上游调节区(URR),E6 / E7和L1区域中的39个CPG位点测定甲基化状态。根据是否持续(≥24?月)或瞬时HPV16感染,参与者将参与者分为两组。持续和患有瞬态感染结果的妇女之间的一般甲基化状态显着差异(p?= 025)。位于L1(NT.?5962)的一个站点在使用HOLM-SIDAK方法(Alphaα= 0.05)校正后的甲基化状态下的统计学显着显着(P?=Δ00048)。 HPV16持续受感染的女性样品的相关分析表明虽然病毒载荷较低,但甲基化更高。该研究表明,L1基因内HPV16基因组的位置5962处的甲基化可能是用于开发持续HPV16感染的预测标记。

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