A Role for HPV16 E5 in Cervical Carcinogenesis

被引:81
作者
Maufort, John P. [1 ,2 ]
Shai, Anny [1 ,2 ]
Pitot, Henry C. [1 ,2 ,3 ]
Lambert, Paul F. [1 ,2 ]
机构
[1] Univ Wisconsin, McArdle Lab Canc Res, Sch Med & Publ Hlth, Madison, WI 53706 USA
[2] Univ Wisconsin, Dept Oncol, Sch Med & Publ Hlth, Madison, WI 53706 USA
[3] Univ Wisconsin, Dept Pathol, Sch Med & Publ Hlth, Madison, WI 53706 USA
关键词
HUMAN-PAPILLOMAVIRUS TYPE-16; GROWTH-FACTOR RECEPTOR; HUMAN FORESKIN KERATINOCYTES; FASL-MEDIATED APOPTOSIS; EPITHELIAL-CELL LINE; VIRAL LIFE-CYCLE; PRODUCTIVE STAGE; GENE-EXPRESSION; DOWN-REGULATION; RAFT CULTURES;
D O I
10.1158/0008-5472.CAN-09-3436
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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. Cancer Res; 70(7); 2924-31. (C) 2010 AACR.
引用
收藏
页码:2924 / 2931
页数:8
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