Dutta Sankhadeep, Chakraborty Chandraditya, Dutta Arup Kumar, Mandal Ranajit Kumar, Roychoudhury Susanta, Basu Partha, Panda Chinmay Kumar
Department of Oncogene Regulation, Chittaranjan National Cancer Institute, Kolkata, West Bengal, India.
Department of Gynaecologic Oncology, Chittaranjan National Cancer Institute, Kolkata, West Bengal, India.
J Clin Pathol. 2015 Mar;68(3):206-11. doi: 10.1136/jclinpath-2014-202611. Epub 2015 Jan 6.
To evaluate how the genetic and epigenetic profile of human papillomavirus 16 (HPV16) changes from asymptomatic cervical infections to cervical cancer (CaCx) development.
HPV16 physical status, methylation of its early-late promoters and its upstream enhancer sequences were analysed in samples from asymptomatic cervical infections (n=89), pre-neoplastic lesions (low and high grade squamous intraepithelial lesions LSIL/HSIL, n=28) and primary CaCx (n=98).
In asymptomatic infection (65%, 58/89) and LSIL/HSIL (57%, 16/28) samples, the episomal form of HPV16 was predominant whereas integration of HPV16 was significantly (p=0.01) higher in CaCx (59%, 57/98). The integrated viral form was also present in asymptomatic (27%, 24/89) and LSIL/HSIL (25%, 7/28) samples. The methylation of the enhancer region was comparable (29-34%) among asymptomatic, LSIL/HSIL and CaCx samples. The episomal form exhibited relatively higher methylation of the early promoter (52%) than that of the late promoter (40%) in asymptomatic infection but the integrated form in asymptomatic carriers showed the opposite methylation pattern (early promoter (42%) vs late-promoter (54%)). A similar pattern was observed in LSIL/HSIL samples, with comparable frequencies (44%) of early and late promoter methylation of the episomal form. However, irrespective of HPV16 physical status, higher methylation of late promoter than that of early promoter was observed in CaCx samples. An inverse correlation was observed between HPV16 integration and overall methylation of the early promoter-enhancer region in CaCx (p=0.05), LSIL/HSIL (p=0.09) and asymptomatic samples (p=0.09).
Our study indicates that integration of HPV16 along with changes in methylation pattern of early and late promoters is essential for neoplastic transformation of asymptomatic cervical infections.
评估人乳头瘤病毒16型(HPV16)从无症状宫颈感染发展为宫颈癌(CaCx)过程中的基因和表观遗传特征变化。
对无症状宫颈感染样本(n = 89)、癌前病变(低级别和高级别鳞状上皮内病变LSIL/HSIL,n = 28)和原发性CaCx样本(n = 98)分析HPV16的物理状态、其早期-晚期启动子及其上游增强子序列的甲基化情况。
在无症状感染样本(65%,58/89)和LSIL/HSIL样本(57%,16/28)中,HPV16的游离形式占主导,而在CaCx样本中HPV16的整合率显著更高(p = 0.01)(59%,57/98)。整合的病毒形式也存在于无症状样本(27%,24/89)和LSIL/HSIL样本(25%,7/28)中。无症状、LSIL/HSIL和CaCx样本中增强子区域的甲基化水平相当(29 - 34%)。在无症状感染中,游离形式的早期启动子甲基化水平(52%)相对高于晚期启动子(40%),但无症状携带者中的整合形式呈现相反的甲基化模式(早期启动子(42%)对晚期启动子(54%))。在LSIL/HSIL样本中观察到类似模式,游离形式的早期和晚期启动子甲基化频率相当(44%)。然而,无论HPV16的物理状态如何,CaCx样本中晚期启动子的甲基化水平均高于早期启动子。在CaCx(p = 0.05)、LSIL/HSIL(p = 0.09)和无症状样本(p = 0.09)中,观察到HPV16整合与早期启动子-增强子区域的总体甲基化呈负相关。
我们的研究表明,HPV16的整合以及早期和晚期启动子甲基化模式的变化对于无症状宫颈感染的肿瘤转化至关重要。