Please use this identifier to cite or link to this item: https://doi.org/10.3390/ijms19061706
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dc.titleHigh-risk human papillomaviral oncogenes E6 and E7 target key cellular pathways to achieve oncogenesis
dc.contributor.authorYeo-Teh N.S.L.
dc.contributor.authorIto Y.
dc.contributor.authorJha S.
dc.date.accessioned2019-03-21T05:58:53Z
dc.date.available2019-03-21T05:58:53Z
dc.date.issued2018
dc.identifier.citationYeo-Teh N.S.L., Ito Y., Jha S. (2018). High-risk human papillomaviral oncogenes E6 and E7 target key cellular pathways to achieve oncogenesis. International Journal of Molecular Sciences 19 (6) : 1-27. ScholarBank@NUS Repository. https://doi.org/10.3390/ijms19061706
dc.identifier.issn16616596
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/152510
dc.description.abstractInfection with high-risk human papillomavirus (HPV) has been linked to several human cancers, the most prominent of which is cervical cancer. The integration of the viral genome into the host genome is one of the manners in which the viral oncogenes E6 and E7 achieve persistent expression. The most well-studied cellular targets of the viral oncogenes E6 and E7 are p53 and pRb, respectively. However, recent research has demonstrated the ability of these two viral factors to target many more cellular factors, including proteins which regulate epigenetic marks and splicing changes in the cell. These have the ability to exert a global change, which eventually culminates to uncontrolled proliferation and carcinogenesis. © 2018 by the authors. Licensee MDPI, Basel, Switzerland.
dc.publisherMDPI AG
dc.sourceScopus
dc.subjectCervical cancer; E6; E7; HPV; Human papillomavirus; Viral oncogenes; Viral-induced cancers
dc.typeReview
dc.contributor.departmentCANCER SCIENCE INSTITUTE OF SINGAPORE
dc.contributor.departmentMEDICINE
dc.contributor.departmentBIOCHEMISTRY
dc.description.doi10.3390/ijms19061706
dc.description.sourcetitleInternational Journal of Molecular Sciences
dc.description.volume19
dc.description.issue6
dc.description.page1-27
dc.published.statepublished
dc.grant.idMOE2014-T3–1-006
dc.grant.idNRF
dc.grant.idR-713-006-014-271
dc.grant.idNMRC
dc.grant.idCBRG-NIG BNIG11nov001
dc.grant.fundingagencyNUS, National University of Singapore
dc.grant.fundingagencyNational Research Foundation Singapore
dc.grant.fundingagencySICS, Singapore Institute for Clinical Sciences
dc.grant.fundingagencyNational Medical Research Council
dc.grant.fundingagencyNMRC, National Medical Research Council
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