Cargando…
Human Papillomavirus Infection in Head and Neck Squamous Cell Carcinomas: Transcriptional Triggers and Changed Disease Patterns
Head and neck squamous cell carcinoma (HNSCC) is a heterogeneous group of cancers. Collectively, HNSCC ranks sixth in incidence rate worldwide. Apart from classical risk factors like tobacco and alcohol, infection of human papillomavirus (HPV) is emerging as a discrete risk factor for HNSCC. HPV-pos...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7738612/ https://www.ncbi.nlm.nih.gov/pubmed/33344262 http://dx.doi.org/10.3389/fcimb.2020.537650 |
_version_ | 1783623155325075456 |
---|---|
author | Aggarwal, Nikita Yadav, Joni Thakur, Kulbhushan Bibban, Rakhi Chhokar, Arun Tripathi, Tanya Bhat, Anjali Singh, Tejveer Jadli, Mohit Singh, Ujala Kashyap, Manoj K. Bharti, Alok C. |
author_facet | Aggarwal, Nikita Yadav, Joni Thakur, Kulbhushan Bibban, Rakhi Chhokar, Arun Tripathi, Tanya Bhat, Anjali Singh, Tejveer Jadli, Mohit Singh, Ujala Kashyap, Manoj K. Bharti, Alok C. |
author_sort | Aggarwal, Nikita |
collection | PubMed |
description | Head and neck squamous cell carcinoma (HNSCC) is a heterogeneous group of cancers. Collectively, HNSCC ranks sixth in incidence rate worldwide. Apart from classical risk factors like tobacco and alcohol, infection of human papillomavirus (HPV) is emerging as a discrete risk factor for HNSCC. HPV-positive HNSCC represent a distinct group of diseases that differ in their clinical presentation. These lesions are well-differentiated, occur at an early age, and have better prognosis. Epidemiological studies have demonstrated a specific increase in the proportions of the HPV-positive HNSCC. HPV-positive and HPV-negative HNSCC lesions display different disease progression and clinical response. For tumorigenic-transformation, HPV essentially requires a permissive cellular environment and host cell factors for induction of viral transcription. As the spectrum of host factors is independent of HPV infection at the time of viral entry, presumably entry of HPV only selects host cells that are permissive to establishment of HPV infection. Growing evidence suggest that HPV plays a more active role in a subset of HNSCC, where they are transcriptionally-active. A variety of factors provide a favorable environment for HPV to become transcriptionally-active. The most notable are the set of transcription factors that have direct binding sites on the viral genome. As HPV does not have its own transcription machinery, it is fully dependent on host transcription factors to complete the life cycle. Here, we review and evaluate the current evidence on level of a subset of host transcription factors that influence viral genome, directly or indirectly, in HNSCC. Since many of these transcription factors can independently promote carcinogenesis, the composition of HPV permissive transcription factors in a tumor can serve as a surrogate marker of a separate molecularly-distinct class of HNSCC lesions including those cases, where HPV could not get a chance to infect but may manifest better prognosis. |
format | Online Article Text |
id | pubmed-7738612 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77386122020-12-17 Human Papillomavirus Infection in Head and Neck Squamous Cell Carcinomas: Transcriptional Triggers and Changed Disease Patterns Aggarwal, Nikita Yadav, Joni Thakur, Kulbhushan Bibban, Rakhi Chhokar, Arun Tripathi, Tanya Bhat, Anjali Singh, Tejveer Jadli, Mohit Singh, Ujala Kashyap, Manoj K. Bharti, Alok C. Front Cell Infect Microbiol Cellular and Infection Microbiology Head and neck squamous cell carcinoma (HNSCC) is a heterogeneous group of cancers. Collectively, HNSCC ranks sixth in incidence rate worldwide. Apart from classical risk factors like tobacco and alcohol, infection of human papillomavirus (HPV) is emerging as a discrete risk factor for HNSCC. HPV-positive HNSCC represent a distinct group of diseases that differ in their clinical presentation. These lesions are well-differentiated, occur at an early age, and have better prognosis. Epidemiological studies have demonstrated a specific increase in the proportions of the HPV-positive HNSCC. HPV-positive and HPV-negative HNSCC lesions display different disease progression and clinical response. For tumorigenic-transformation, HPV essentially requires a permissive cellular environment and host cell factors for induction of viral transcription. As the spectrum of host factors is independent of HPV infection at the time of viral entry, presumably entry of HPV only selects host cells that are permissive to establishment of HPV infection. Growing evidence suggest that HPV plays a more active role in a subset of HNSCC, where they are transcriptionally-active. A variety of factors provide a favorable environment for HPV to become transcriptionally-active. The most notable are the set of transcription factors that have direct binding sites on the viral genome. As HPV does not have its own transcription machinery, it is fully dependent on host transcription factors to complete the life cycle. Here, we review and evaluate the current evidence on level of a subset of host transcription factors that influence viral genome, directly or indirectly, in HNSCC. Since many of these transcription factors can independently promote carcinogenesis, the composition of HPV permissive transcription factors in a tumor can serve as a surrogate marker of a separate molecularly-distinct class of HNSCC lesions including those cases, where HPV could not get a chance to infect but may manifest better prognosis. Frontiers Media S.A. 2020-12-02 /pmc/articles/PMC7738612/ /pubmed/33344262 http://dx.doi.org/10.3389/fcimb.2020.537650 Text en Copyright © 2020 Aggarwal, Yadav, Thakur, Bibban, Chhokar, Tripathi, Bhat, Singh, Jadli, Singh, Kashyap and Bharti http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cellular and Infection Microbiology Aggarwal, Nikita Yadav, Joni Thakur, Kulbhushan Bibban, Rakhi Chhokar, Arun Tripathi, Tanya Bhat, Anjali Singh, Tejveer Jadli, Mohit Singh, Ujala Kashyap, Manoj K. Bharti, Alok C. Human Papillomavirus Infection in Head and Neck Squamous Cell Carcinomas: Transcriptional Triggers and Changed Disease Patterns |
title | Human Papillomavirus Infection in Head and Neck Squamous Cell Carcinomas: Transcriptional Triggers and Changed Disease Patterns |
title_full | Human Papillomavirus Infection in Head and Neck Squamous Cell Carcinomas: Transcriptional Triggers and Changed Disease Patterns |
title_fullStr | Human Papillomavirus Infection in Head and Neck Squamous Cell Carcinomas: Transcriptional Triggers and Changed Disease Patterns |
title_full_unstemmed | Human Papillomavirus Infection in Head and Neck Squamous Cell Carcinomas: Transcriptional Triggers and Changed Disease Patterns |
title_short | Human Papillomavirus Infection in Head and Neck Squamous Cell Carcinomas: Transcriptional Triggers and Changed Disease Patterns |
title_sort | human papillomavirus infection in head and neck squamous cell carcinomas: transcriptional triggers and changed disease patterns |
topic | Cellular and Infection Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7738612/ https://www.ncbi.nlm.nih.gov/pubmed/33344262 http://dx.doi.org/10.3389/fcimb.2020.537650 |
work_keys_str_mv | AT aggarwalnikita humanpapillomavirusinfectioninheadandnecksquamouscellcarcinomastranscriptionaltriggersandchangeddiseasepatterns AT yadavjoni humanpapillomavirusinfectioninheadandnecksquamouscellcarcinomastranscriptionaltriggersandchangeddiseasepatterns AT thakurkulbhushan humanpapillomavirusinfectioninheadandnecksquamouscellcarcinomastranscriptionaltriggersandchangeddiseasepatterns AT bibbanrakhi humanpapillomavirusinfectioninheadandnecksquamouscellcarcinomastranscriptionaltriggersandchangeddiseasepatterns AT chhokararun humanpapillomavirusinfectioninheadandnecksquamouscellcarcinomastranscriptionaltriggersandchangeddiseasepatterns AT tripathitanya humanpapillomavirusinfectioninheadandnecksquamouscellcarcinomastranscriptionaltriggersandchangeddiseasepatterns AT bhatanjali humanpapillomavirusinfectioninheadandnecksquamouscellcarcinomastranscriptionaltriggersandchangeddiseasepatterns AT singhtejveer humanpapillomavirusinfectioninheadandnecksquamouscellcarcinomastranscriptionaltriggersandchangeddiseasepatterns AT jadlimohit humanpapillomavirusinfectioninheadandnecksquamouscellcarcinomastranscriptionaltriggersandchangeddiseasepatterns AT singhujala humanpapillomavirusinfectioninheadandnecksquamouscellcarcinomastranscriptionaltriggersandchangeddiseasepatterns AT kashyapmanojk humanpapillomavirusinfectioninheadandnecksquamouscellcarcinomastranscriptionaltriggersandchangeddiseasepatterns AT bhartialokc humanpapillomavirusinfectioninheadandnecksquamouscellcarcinomastranscriptionaltriggersandchangeddiseasepatterns |