| Literature DB >> 30415951 |
Shashi Kiran1, Ashraf Dar1, Samarendra K Singh1, Kyung Yong Lee1, Anindya Dutta2.
Abstract
High-risk human papilloma viruses (HPVs) cause cervical, anal, and oropharyngeal cancers, unlike the low-risk HPVs, which cause benign lesions. E6 oncoproteins from the high-risk strains are essential for cell proliferation and transformation in HPV-induced cancers. We report that a cellular deubiquitinase, USP46, is selectively recruited by the E6 of high-risk, but not low-risk, HPV to deubiqutinate and stabilize Cdt2/DTL. Stabilization of Cdt2, a component of the CRL4Cdt2 E3 ubiquitin ligase, limits the level of Set8, an epigenetic writer, and promotes cell proliferation. USP46 is essential for the proliferation of HPV-transformed cells, but not of cells without HPV. Cdt2 is elevated in human cervical cancers and knockdown of USP46 inhibits HPV-transformed tumor growth in xenografts. Recruitment of a cellular deubiquitinase to stabilize key cellular proteins is an important activity of oncogenic E6, and the importance of E6-USP46-Cdt2-Set8 pathway in HPV-induced cancers makes USP46 a target for the therapy of such cancers.Entities:
Keywords: Cdt2; E6; HPV; USP46; cervical cancer; deubiquitinase; oncogenic virus
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Year: 2018 PMID: 30415951 PMCID: PMC6294304 DOI: 10.1016/j.molcel.2018.09.019
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970