DNA Methylation Changes in Human Papillomavirus-Driven Head and Neck Cancers
Disruption of DNA methylation patterns is one of the hallmarks of cancer. Similar to other cancer types, human papillomavirus (HPV)-driven head and neck cancer (HNC) also reveals alterations in its methylation profile. The intrinsic ability of HPV oncoproteins E6 and E7 to interfere with DNA methylt...
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Published in: | Cells (Basel, Switzerland) Vol. 9; no. 6; p. 1359 |
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Abstract | Disruption of DNA methylation patterns is one of the hallmarks of cancer. Similar to other cancer types, human papillomavirus (HPV)-driven head and neck cancer (HNC) also reveals alterations in its methylation profile. The intrinsic ability of HPV oncoproteins E6 and E7 to interfere with DNA methyltransferase activity contributes to these methylation changes. There are many genes that have been reported to be differentially methylated in HPV-driven HNC. Some of these genes are involved in major cellular pathways, indicating that DNA methylation, at least in certain instances, may contribute to the development and progression of HPV-driven HNC. Furthermore, the HPV genome itself becomes a target of the cellular DNA methylation machinery. Some of these methylation changes appearing in the viral long control region (LCR) may contribute to uncontrolled oncoprotein expression, leading to carcinogenesis. Consistent with these observations, demethylation therapy appears to have significant effects on HPV-driven HNC. This review article comprehensively summarizes DNA methylation changes and their diagnostic and therapeutic indications in HPV-driven HNC. |
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AbstractList | Disruption of DNA methylation patterns is one of the hallmarks of cancer. Similar to other cancer types, human papillomavirus (HPV)-driven head and neck cancer (HNC) also reveals alterations in its methylation profile. The intrinsic ability of HPV oncoproteins E6 and E7 to interfere with DNA methyltransferase activity contributes to these methylation changes. There are many genes that have been reported to be differentially methylated in HPV-driven HNC. Some of these genes are involved in major cellular pathways, indicating that DNA methylation, at least in certain instances, may contribute to the development and progression of HPV-driven HNC. Furthermore, the HPV genome itself becomes a target of the cellular DNA methylation machinery. Some of these methylation changes appearing in the viral long control region (LCR) may contribute to uncontrolled oncoprotein expression, leading to carcinogenesis. Consistent with these observations, demethylation therapy appears to have significant effects on HPV-driven HNC. This review article comprehensively summarizes DNA methylation changes and their diagnostic and therapeutic indications in HPV-driven HNC. |
Author | Kenny, Liz Punyadeera, Chamindie Langton-Lockton, Julian Vasani, Sarju Ekanayake Weeramange, Chameera Tang, Kai Dun |
AuthorAffiliation | 1 Saliva & Liquid Biopsy Translational Research Team, Institute of Health and Biomedical Innovation, School of Biomedical Sciences, Queensland University of Technology (QUT), Queensland 4059, Australia; s.weeramange@qut.edu.au (C.E.W.); kai.tang@qut.edu.au (K.D.T.) 3 Department of Medical Laboratory Sciences, Faculty of Health Sciences, The Open University of Sri Lanka, Nugegoda 10250, Sri Lanka 4 Department of Otolaryngology, Royal Brisbane and Women’s Hospital, Queensland 4029, Australia; Sarju.Vasani@health.qld.gov.au 5 School of Medicine, The University of Queensland, Queensland 4006, Australia; lizkenny@bigpond.net.au 8 Central Integrated Regional Cancer Service, Queensland Health, Queensland 4001, Australia 2 Translational Research Institute, Queensland University of Technology (QUT), Queensland 4102, Australia 7 Department of Cancer Care Services, Royal Brisbane and Women’s Hospital, Queensland 4029, Australia 6 Metro-North Sexual Health and HIV Service, Queensland 4000, Australia; Jul |
AuthorAffiliation_xml | – name: 5 School of Medicine, The University of Queensland, Queensland 4006, Australia; lizkenny@bigpond.net.au – name: 8 Central Integrated Regional Cancer Service, Queensland Health, Queensland 4001, Australia – name: 2 Translational Research Institute, Queensland University of Technology (QUT), Queensland 4102, Australia – name: 3 Department of Medical Laboratory Sciences, Faculty of Health Sciences, The Open University of Sri Lanka, Nugegoda 10250, Sri Lanka – name: 7 Department of Cancer Care Services, Royal Brisbane and Women’s Hospital, Queensland 4029, Australia – name: 4 Department of Otolaryngology, Royal Brisbane and Women’s Hospital, Queensland 4029, Australia; Sarju.Vasani@health.qld.gov.au – name: 6 Metro-North Sexual Health and HIV Service, Queensland 4000, Australia; Julian.LangtonLockton@health.qld.gov.au – name: 1 Saliva & Liquid Biopsy Translational Research Team, Institute of Health and Biomedical Innovation, School of Biomedical Sciences, Queensland University of Technology (QUT), Queensland 4059, Australia; s.weeramange@qut.edu.au (C.E.W.); kai.tang@qut.edu.au (K.D.T.) |
Author_xml | – sequence: 1 givenname: Chameera surname: Ekanayake Weeramange fullname: Ekanayake Weeramange, Chameera organization: Department of Medical Laboratory Sciences, Faculty of Health Sciences, The Open University of Sri Lanka, 10250 Nugegoda, Sri Lanka – sequence: 2 givenname: Kai Dun surname: Tang fullname: Tang, Kai Dun organization: Queensland University of Technology (QUT), Translational Research Institute, Queensland 4102, Australia – sequence: 3 givenname: Sarju surname: Vasani fullname: Vasani, Sarju organization: School of Medicine, The University of Queensland, Queensland 4006, Australia – sequence: 4 givenname: Julian surname: Langton-Lockton fullname: Langton-Lockton, Julian organization: Metro-North Sexual Health and HIV Service, Queensland 4000, Australia – sequence: 5 givenname: Liz surname: Kenny fullname: Kenny, Liz organization: Central Integrated Regional Cancer Service, Queensland Health, Queensland 4001, Australia – sequence: 6 givenname: Chamindie surname: Punyadeera fullname: Punyadeera, Chamindie organization: Queensland University of Technology (QUT), Translational Research Institute, Queensland 4102, Australia |
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Keywords | head and neck cancer DNA methylation human papillomavirus |
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SubjectTerms | Alphapapillomavirus - genetics Alphapapillomavirus - physiology Carcinogenesis - genetics Carcinogenesis - pathology DNA methylation DNA Methylation - genetics DNA, Viral - genetics Genome, Viral head and neck cancer Head and Neck Neoplasms - diagnosis Head and Neck Neoplasms - genetics Head and Neck Neoplasms - therapy Head and Neck Neoplasms - virology human papillomavirus Humans Review |
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Title | DNA Methylation Changes in Human Papillomavirus-Driven Head and Neck Cancers |
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