Oncogenic human papillomaviruses block expression of the B-cell translocation gene-2 tumor suppressor gene

被引:5
|
作者
Cullmann, Claire [1 ]
Hoppe-Seyler, Karin [1 ]
Dymalla, Susanne [1 ]
Lohrey, Claudia [1 ]
Scheffner, Martin [2 ]
Duerst, Matthias [3 ]
Hoppe-Seyler, Felix [1 ]
机构
[1] German Canc Res Ctr, Mol Therapy Virus Assoc Canc, D-6900 Heidelberg, Germany
[2] Univ Konstanz, Dept Biol, Constance, Germany
[3] Frauenklin FSU Jena, Jena, Germany
关键词
viral carcinogenesis; human papillomavirus; E6; cervical cancers; tumor suppressor genes; BTG2; POSITIVE CANCER-CELLS; GROWTH-INHIBITION; DOWN-REGULATION; E6; ONCOPROTEIN; RETINOIC ACID; P53; PROTEIN; BTG2; CARCINOMA; OVEREXPRESSION;
D O I
10.1002/ijc.24671
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Human papillomavirus (HPV)-induced carcinogenesis is critically dependent on the activities of the viral E6 and E7 oncogenes. Here, we demonstrate that expression of the putative tumor suppressor gene B-cell translocation gene-2 (BTG2) is reinduced in HPV16- and HPV18-positive cancer cells on silencing of viral oncogene expression, indicating that BTG2 is repressed by oncogenic HPVs. Inhibition of BTG2 expression was mediated by the HPV E6 oncogene and occurred in a p53-dependent manner. Luciferase reporter gene analyses revealed that BTG2 repression takes place at the transcriptional level and is dependent on the integrity of the major p53-response element within the BTG2 promoter. Ectopic expression of BTG2 acted antiproliferative in cervical cancer cells. Tissue specimens commonly exhibited reduced BTG2 protein levels in HPV-positive high-grade lesions (CIN2/3) and cervical carcinomas, when compared with normal cervical epithelium. These findings identify the antiproliferative BTG2 gene as a novel cellular target blocked by the HPV E6 oncoprotein. (C) 2009 UICC
引用
收藏
页码:2014 / 2020
页数:7
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