Cancer Genetics Research Laboratory, Division of Cancer Epidemiology and Genetics, Leidos Biomedical Research Inc., National Laboratory for Cancer Research, Gaithersburg, Maryland.
Laboratory of Translational Genomics, Division of Cancer Epidemiology and Genetics, NCI, Gaithersburg, Maryland.
Cancer Res. 2020 Sep 15;80(18):3803-3809. doi: 10.1158/0008-5472.CAN-20-0029. Epub 2020 Jul 6.
Human papillomavirus (HPV) 16 displays substantial sequence variation; four HPV16 lineages (A, B, C, and D) have been described as well as multiple sublineages. To identify molecular events associated with HPV16 carcinogenesis, we evaluated viral variation, the integration of HPV16, and somatic mutation in 96 cervical cancer samples from Guatemala. A total of 65% (62/96) of the samples had integrated HPV16 sequences and integration was associated with an earlier age of diagnosis and premenopausal disease. HPV16 integration sites were broadly distributed in the genome, but in one tumor, HPV16 integrated into the promoter of the IFN regulatory factor 4 () gene, which plays an important role in the regulation of the IFN response to viral infection. The HPV16 D2 and D3 sublineages were found in 23% and 30% of the tumors, respectively, and were significantly associated with adenocarcinoma. D2-positive tumors had a higher rate of integration, earlier age of diagnosis, and a lower rate of somatic mutation, whereas D3-positive tumors were less likely to integrate, had later age of diagnosis, and exhibited a higher rate of somatic mutation. In conclusion, Guatemalan cervical tumors have a high frequency of very high-risk HPV16 D2 and D3 sublineages harboring distinct histology, which may help guide future therapeutic strategies to target the tumor and reduce recurrence. SIGNIFICANCE: This study details the biological and molecular properties of the most pathogenic forms of HPV16, the cause of the majority of cervical cancers.
人乳头瘤病毒 (HPV) 16 显示出大量的序列变异;已经描述了 HPV16 的四个谱系 (A、B、C 和 D) 以及多个亚谱系。为了确定与 HPV16 致癌相关的分子事件,我们评估了来自危地马拉的 96 例宫颈癌样本中的病毒变异、HPV16 的整合以及体细胞突变。总共有 65%(62/96)的样本具有整合的 HPV16 序列,并且整合与更早的诊断年龄和绝经前疾病相关。HPV16 整合位点广泛分布在基因组中,但在一个肿瘤中,HPV16 整合到干扰素调节因子 4 () 基因的启动子中,该基因在调节病毒感染的 IFN 反应中发挥重要作用。HPV16 D2 和 D3 亚谱系分别在 23%和 30%的肿瘤中发现,与腺癌显著相关。D2 阳性肿瘤的整合率更高,诊断年龄更早,体细胞突变率更低,而 D3 阳性肿瘤的整合率较低,诊断年龄较晚,体细胞突变率较高。总之,危地马拉宫颈肿瘤中存在高频率的高危 HPV16 D2 和 D3 亚谱系,具有不同的组织学特征,这可能有助于指导未来针对肿瘤的治疗策略,以降低复发率。意义:本研究详细描述了 HPV16 最具致病性形式的生物学和分子特性,这是大多数宫颈癌的病因。