Human papillomavirus type 16 E7 perturbs DREAM to promote cellular proliferation and mitotic gene expression.

Abstract

The study of the small DNA tumor viruses continues to provide valuable new insights into oncogenesis and fundamental biological processes. Although much has already been revealed about how the human papillomaviruses (HPVs) can transform cells and contribute to cervical and oropharyngeal cancer, there clearly is much more to learn. In this issue of Oncogene, Pang et al., doi:10.1038/onc.2013.426, demonstrate that the high-risk HPV16 E7 oncogene can promote cellular proliferation by interacting with the DREAM (DP, RB-like, E2F and MuvB) complex at two distinct phases of the cell cycle. Consistent with earlier work, HPV16 E7 can bind to the retinoblastoma tumor suppressor (RB) family member p130 (RBL2) protein and promote its proteasome-mediated destruction thereby disrupting the DREAM complex and can prevent exit from the cell cycle into quiescence. In addition, they demonstrate that HPV16 E7 can bind to MuvB core complex in association with BMYB and FOXM1 and activate gene expression during the G2 and M phase of the cell cycle. Thus, HPV16 E7 acts to prevent exit from the cell cycle entry and promotes mitotic proliferation and may account for the high levels of FOXM1 often observed in poor-risk cervical cancers.

• Authors: J A DeCaprio
• Journal: Oncogene (Oncogene) Vol. 33 Issue 31 Pg. 4036-8 (Jul 31 2014) ISSN: 1476-5594 [Electronic] England
• PMID: 24166507 (Publication Type: Journal Article, Comment)

Chemical References

• Cell Cycle Proteins
• FOXM1 protein, human
• Forkhead Box Protein M1
• Forkhead Transcription Factors
• LIN9 protein, human
• MYBL2 protein, human
• Nuclear Proteins
• Papillomavirus E7 Proteins
• Trans-Activators
• Tumor Suppressor Proteins

Topics

• Cell Cycle Proteins (metabolism)
• Female
• Forkhead Box Protein M1
• Forkhead Transcription Factors (metabolism)
• Gene Expression Regulation, Neoplastic
• Human papillomavirus 16 (metabolism)
• Humans
• Nuclear Proteins (metabolism)
• Papillomavirus E7 Proteins (metabolism)
• Trans-Activators (metabolism)
• Tumor Suppressor Proteins (metabolism)
• Uterine Cervical Neoplasms (virology)