Advances in human papillomavirus detection and molecular understanding in head and neck cancers: Implications for clinical management.
- Publisher:
- WILEY
- Publication Type:
- Journal Article
- Citation:
- J Med Virol, 2024, 96, (6), pp. e29746
- Issue Date:
- 2024-06
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Full metadata record
Field | Value | Language |
---|---|---|
dc.contributor.author | Tran, NH | |
dc.contributor.author |
Sais, D https://orcid.org/0000-0002-5859-1398 |
|
dc.contributor.author |
Tran, N https://orcid.org/0000-0001-7747-2530 |
|
dc.date.accessioned | 2024-11-05T02:10:25Z | |
dc.date.available | 2024-06-08 | |
dc.date.available | 2024-11-05T02:10:25Z | |
dc.date.issued | 2024-06 | |
dc.identifier.citation | J Med Virol, 2024, 96, (6), pp. e29746 | |
dc.identifier.issn | 0146-6615 | |
dc.identifier.issn | 1096-9071 | |
dc.identifier.uri | http://hdl.handle.net/10453/181741 | |
dc.description.abstract | Head and neck cancers (HNCs), primarily head and neck squamous cell carcinoma (HNSCC), are associated with high-risk human papillomavirus (HR HPV), notably HPV16 and HPV18. HPV status guides treatment and predicts outcomes, with distinct molecular pathways in HPV-driven HNSCC influencing survival rates. HNC incidence is rising globally, with regional variations reflecting diverse risk factors, including tobacco, alcohol, and HPV infection. Oropharyngeal cancers attributed to HPV have significantly increased, particularly in regions like the United States. The HPV16 genome, characterized by oncoproteins E6 and E7, disrupts crucial cell cycle regulators, including tumor protein p53 (TP53) and retinoblastoma (Rb), contributing to HNSCC pathogenesis. P16 immunohistochemistry (IHC) is a reliable surrogate marker for HPV16 positivity, while in situ hybridization and polymerase chain reaction (PCR) techniques, notably reverse transcription-quantitative PCR (RT-qPCR), offer sensitive HPV detection. Liquid-based RT-qPCR, especially in saliva, shows promise for noninvasive HPV detection, offering simplicity, cost-effectiveness, and patient compliance. These molecular advancements enhance diagnostic accuracy, guide treatment decisions, and improve patient outcomes in HNC management. In conclusion, advances in HPV detection and molecular understanding have significant clinical management implications. Integrating these advancements into routine practice could ultimately improve patient outcomes. | |
dc.format | ||
dc.language | eng | |
dc.publisher | WILEY | |
dc.relation.ispartof | J Med Virol | |
dc.relation.isbasedon | 10.1002/jmv.29746 | |
dc.rights | info:eu-repo/semantics/openAccess | |
dc.subject | 0605 Microbiology, 1108 Medical Microbiology | |
dc.subject.classification | Virology | |
dc.subject.classification | 3107 Microbiology | |
dc.subject.classification | 3202 Clinical sciences | |
dc.subject.classification | 3207 Medical microbiology | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Papillomavirus Infections | |
dc.subject.mesh | Head and Neck Neoplasms | |
dc.subject.mesh | Squamous Cell Carcinoma of Head and Neck | |
dc.subject.mesh | Human papillomavirus 16 | |
dc.subject.mesh | Papillomaviridae | |
dc.subject.mesh | Human papillomavirus 18 | |
dc.subject.mesh | Human Papillomavirus Viruses | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Papillomaviridae | |
dc.subject.mesh | Papillomavirus Infections | |
dc.subject.mesh | Head and Neck Neoplasms | |
dc.subject.mesh | Human papillomavirus 18 | |
dc.subject.mesh | Human papillomavirus 16 | |
dc.subject.mesh | Squamous Cell Carcinoma of Head and Neck | |
dc.subject.mesh | Human Papillomavirus Viruses | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Papillomavirus Infections | |
dc.subject.mesh | Head and Neck Neoplasms | |
dc.subject.mesh | Squamous Cell Carcinoma of Head and Neck | |
dc.subject.mesh | Human papillomavirus 16 | |
dc.subject.mesh | Papillomaviridae | |
dc.subject.mesh | Human papillomavirus 18 | |
dc.subject.mesh | Human Papillomavirus Viruses | |
dc.title | Advances in human papillomavirus detection and molecular understanding in head and neck cancers: Implications for clinical management. | |
dc.type | Journal Article | |
utslib.citation.volume | 96 | |
utslib.location.activity | United States | |
utslib.for | 0605 Microbiology | |
utslib.for | 1108 Medical Microbiology | |
pubs.organisational-group | University of Technology Sydney | |
pubs.organisational-group | University of Technology Sydney/Faculty of Engineering and Information Technology | |
pubs.organisational-group | University of Technology Sydney/Faculty of Engineering and Information Technology/School of Biomedical Engineering | |
pubs.organisational-group | University of Technology Sydney/UTS Groups | |
pubs.organisational-group | University of Technology Sydney/UTS Groups/Centre for Health Technologies (CHT) | |
utslib.copyright.status | open_access | * |
dc.rights.license | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (CC BY-NC-ND 4.0). To view a copy of this license, visit https://creativecommons.org/licenses/by-nc-nd/4.0/ | |
dc.date.updated | 2024-11-05T02:10:22Z | |
pubs.issue | 6 | |
pubs.publication-status | Published | |
pubs.volume | 96 | |
utslib.citation.issue | 6 |
Abstract:
Head and neck cancers (HNCs), primarily head and neck squamous cell carcinoma (HNSCC), are associated with high-risk human papillomavirus (HR HPV), notably HPV16 and HPV18. HPV status guides treatment and predicts outcomes, with distinct molecular pathways in HPV-driven HNSCC influencing survival rates. HNC incidence is rising globally, with regional variations reflecting diverse risk factors, including tobacco, alcohol, and HPV infection. Oropharyngeal cancers attributed to HPV have significantly increased, particularly in regions like the United States. The HPV16 genome, characterized by oncoproteins E6 and E7, disrupts crucial cell cycle regulators, including tumor protein p53 (TP53) and retinoblastoma (Rb), contributing to HNSCC pathogenesis. P16 immunohistochemistry (IHC) is a reliable surrogate marker for HPV16 positivity, while in situ hybridization and polymerase chain reaction (PCR) techniques, notably reverse transcription-quantitative PCR (RT-qPCR), offer sensitive HPV detection. Liquid-based RT-qPCR, especially in saliva, shows promise for noninvasive HPV detection, offering simplicity, cost-effectiveness, and patient compliance. These molecular advancements enhance diagnostic accuracy, guide treatment decisions, and improve patient outcomes in HNC management. In conclusion, advances in HPV detection and molecular understanding have significant clinical management implications. Integrating these advancements into routine practice could ultimately improve patient outcomes.
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