Department of Oncology and the McArdle Laboratory for Cancer Research, University of Wisconsin School of Medicine and Public Health, Madison, WI 53706, USA.
Cancer Res. 2010 Apr 1;70(7):2924-31. doi: 10.1158/0008-5472.CAN-09-3436. Epub 2010 Mar 23.
A subset of the mucosotropic human papillomaviruses (HPV), including HPV16, are etiologic agents for the vast majority of cervical cancers, other anogenital cancers, and a subset of head and neck squamous cell carcinomas. HPV16 encodes three oncogenes: E5, E6, and E7. Although E6 and E7 have been well-studied and clearly shown to be important contributors to these cancers, less is known about E5. In this study, we used E5 transgenic mice to investigate the role of E5 in cervical cancer. When treated for 6 months with estrogen, a cofactor for cervical carcinogenesis, E5 transgenic mice developed more severe neoplastic cervical disease than similarly treated nontransgenic mice, although no frank cancers were detected. In addition, E5 when combined with either E6 or E7 induced more severe neoplastic disease than seen in mice expressing only one viral oncogene. Prolonged treatment of E5 transgenic mice with exogenous estrogen uncovered an ability of E5 to cause frank cancer. These data indicate that E5 acts as an oncogene in the reproductive tracts of female mice.
黏膜型人乳头瘤病毒(HPV)的一个亚群,包括 HPV16,是绝大多数宫颈癌、其他肛门生殖器癌以及一部分头颈部鳞状细胞癌的病因。HPV16 编码三个致癌基因:E5、E6 和 E7。尽管 E6 和 E7 已得到充分研究,并明确表明是这些癌症的重要促成因素,但对 E5 的了解较少。在这项研究中,我们使用 E5 转基因小鼠来研究 E5 在宫颈癌中的作用。当用雌激素(宫颈癌发生的协同因子)处理 6 个月时,E5 转基因小鼠比经同样处理的非转基因小鼠发展出更严重的肿瘤性宫颈疾病,尽管未检测到明显的癌症。此外,E5 与 E6 或 E7 联合表达时,引起的肿瘤性疾病比仅表达一种病毒致癌基因的小鼠更严重。对 E5 转基因小鼠进行外源性雌激素的长期处理揭示了 E5 导致癌症的能力。这些数据表明 E5 在雌性小鼠的生殖道中作为致癌基因发挥作用。