Cellular binding partners of the human papillomavirus E6 protein

被引:0
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作者
Sandy S. Tungteakkhun
Penelope J. Duerksen-Hughes
机构
[1] Loma Linda University School of Medicine,Department of Basic Sciences
来源
Archives of Virology | 2008年 / 153卷
关键词
Paxillin; Death Effector Domain; Long Control Region; Epithelial Tight Junction; Epithelial Organization;
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摘要
The high-risk strains of human papillomavirus (HR-HPV) are known to be causative agents of cervical cancer and have recently also been implicated in cancers of the oropharynx. E6 is a potent oncogene of HR-HPVs, and its role in the progression to malignancy has been and continues to be explored. E6 is known to interact with and subsequently inactivate numerous cellular proteins pivotal in the mediation of apoptosis, transcription of tumor suppressor genes, maintenance of epithelial organization, and control of cell proliferation. Binding of E6 to these proteins cumulatively contributes to the oncogenic potential of HPV. This paper provides an overview of these cellular protein partners of HR-E6, the motifs known to mediate oncoprotein binding, and the agents that have the potential to interfere with E6 expression and activity and thus prevent the subsequent progression to oncogenesis.
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