| Literature DB >> 19047178 |
Daniela Holland1, Karin Hoppe-Seyler, Bettina Schuller, Claudia Lohrey, Julia Maroldt, Matthias Dürst, Felix Hoppe-Seyler.
Abstract
The malignant phenotype of human papillomavirus (HPV)-positive cancer cells is maintained by the activity of the viral E6 and E7 genes. Here, we identified the polycomb group gene enhancer of zeste homologue 2 (EZH2) as a novel downstream target for the viral oncogenes in HPV-transformed cells. EZH2 expression was activated by HPV16 E7 at the transcriptional level via E7-mediated release of E2F from pocket proteins. RNA interference analyses showed that continuous EZH2 expression is required for the proliferation of HPV-positive tumor cells by stimulating cell cycle progression at the G1-S boundary. In addition to its growth-promoting activity, EZH2 also contributed to the apoptotic resistance of cervical cancer cells. Furthermore, we found that HPV-positive dysplastic and tumorigenic cervical lesions were characterized by high levels of EZH2 protein in vivo. We conclude that the E7 target gene EZH2 is a major determinant for the proliferation of HPV-positive cancer cells and contributes to their apoptotic resistance. Moreover, EZH2 may serve as a novel therapeutic target for the treatment of cervical cancer.Entities:
Mesh:
Substances:
Year: 2008 PMID: 19047178 DOI: 10.1158/0008-5472.CAN-08-1134
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701