Department of Pathology, School of Medicine, School of Public Health, University of Washington, Seattle, Washington, United States of America.
PLoS One. 2011;6(8):e23897. doi: 10.1371/journal.pone.0023897. Epub 2011 Aug 24.
The clinical relevance of human papillomavirus type 16 (HPV16) DNA methylation has not been well documented, although its role in modulation of viral transcription is recognized.
Study subjects were 211 women attending Planned Parenthood clinics in Western Washington for routine Papanicolaou screening who were HPV16 positive at the screening and/or subsequent colposcopy visit. Methylation of 11 CpG dinucleotides in the 3' end of the long control region of the HPV16 genome was examined by sequencing the cloned polymerase chain reaction products. The association between risk of CIN2/3 and degree of CpG methylation was estimated using a logistic regression model.
CIN2/3 was histologically confirmed in 94 (44.5%) of 211 HPV16 positive women. The likelihood of being diagnosed as CIN2/3 increased significantly with decreasing numbers of methylated CpGs (meCpGs) in the 3' end of the long control region (P(for trend) = 0.003). After adjusting for HPV16 variants, number of HPV16-positive visits, current smoking status and lifetime number of male sex partners, the odds ratio for the association of CIN2/3 with ≥4 meCpGs was 0.31 (95% confidence interval, 0.12-0.79). The proportion of ≥4 meCpGs decreased appreciably as the severity of the cervical lesion increased (P(for trend) = 0.001). The inverse association remained similar when CIN3 was used as the clinical endpoint. Although not statistically significant, the ≥4 meCpGs-related risk reduction was more substantial among current, as compared to noncurrent, smokers.
Results suggest that degree of the viral genome methylation is related to the outcome of an HPV16 cervical infection.
人乳头瘤病毒 16 型(HPV16)DNA 甲基化的临床相关性尚未得到充分证实,尽管其在病毒转录调节中的作用已得到认可。
研究对象为 211 名在华盛顿西部计划生育诊所接受常规巴氏涂片筛查的女性,她们在筛查时以及随后的阴道镜检查中 HPV16 呈阳性。通过测序克隆聚合酶链反应产物,检测 HPV16 基因组 3'端长控制区 11 个 CpG 二核苷酸的甲基化。使用逻辑回归模型估计 CIN2/3 风险与 CpG 甲基化程度之间的关联。
211 名 HPV16 阳性妇女中,94 名(44.5%)组织学确诊为 CIN2/3。3'端长控制区甲基化 CpG 数量(meCpGs)减少与 CIN2/3 诊断呈显著正相关(P(趋势)=0.003)。在校正 HPV16 变体、HPV16 阳性就诊次数、当前吸烟状况和终生男性性伴侣数量后,CIN2/3 与≥4 个 meCpGs 相关的比值比为 0.31(95%置信区间,0.12-0.79)。随着宫颈病变严重程度的增加,≥4 个 meCpGs 的比例明显下降(P(趋势)=0.001)。当 CIN3 作为临床终点时,这种负相关仍然相似。尽管没有统计学意义,但与非当前吸烟者相比,当前吸烟者中≥4 个 meCpGs 相关的风险降低更为显著。
结果表明,病毒基因组甲基化程度与 HPV16 宫颈感染的结局相关。