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Frequent KRAS and HRAS mutations in squamous cell papillomas of the head and neck
Squamous cell papilloma (SCP) is a benign neoplasm of the head and neck. Human papillomavirus (HPV) has been reported to be a tumourigenic factor for SCP. However, not all SCPs are positive for HPV, suggesting that other possible mechanisms are involved in their development. In this study, we examin...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7164371/ https://www.ncbi.nlm.nih.gov/pubmed/31960612 http://dx.doi.org/10.1002/cjp2.157 |
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author | Sasaki, Eiichi Masago, Katsuhiro Fujita, Shiro Hanai, Nobuhiro Yatabe, Yasushi |
author_facet | Sasaki, Eiichi Masago, Katsuhiro Fujita, Shiro Hanai, Nobuhiro Yatabe, Yasushi |
author_sort | Sasaki, Eiichi |
collection | PubMed |
description | Squamous cell papilloma (SCP) is a benign neoplasm of the head and neck. Human papillomavirus (HPV) has been reported to be a tumourigenic factor for SCP. However, not all SCPs are positive for HPV, suggesting that other possible mechanisms are involved in their development. In this study, we examined the mutational status of 51 SCPs using targeted panel sequencing in addition to HPV status using GP5+/GP6+ PCR. HPV DNA was detected in 6 (12%) SCPs, while KRAS and HRAS mutations were detected in 18 (35%) and 17 (33%) SCPs, respectively. Notably, KRAS mutations, HRAS mutations and HPV infection were mutually exclusive. The larynx and trachea (4/7, 57%) were more preferentially infected by HPV than the other sites (2/44, 5%, p = 0.0019) and HPV was associated with multifocal development (4/5, 80%). In contrast, KRAS and HRAS mutations in SCPs were evenly distributed across the anatomical sites and found only in single SCPs. In conclusion, this study demonstrated that HPV was not frequently involved in SCPs and that RAS mutations were more common alterations. In contrast to inverted sinonasal papillomas and oncocytic sinonasal papillomas, SCP may not be a precursor lesion of carcinoma, because these aetiological events in SCP are distinct from squamous cell carcinoma in the same sites. |
format | Online Article Text |
id | pubmed-7164371 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71643712020-04-20 Frequent KRAS and HRAS mutations in squamous cell papillomas of the head and neck Sasaki, Eiichi Masago, Katsuhiro Fujita, Shiro Hanai, Nobuhiro Yatabe, Yasushi J Pathol Clin Res Original Articles Squamous cell papilloma (SCP) is a benign neoplasm of the head and neck. Human papillomavirus (HPV) has been reported to be a tumourigenic factor for SCP. However, not all SCPs are positive for HPV, suggesting that other possible mechanisms are involved in their development. In this study, we examined the mutational status of 51 SCPs using targeted panel sequencing in addition to HPV status using GP5+/GP6+ PCR. HPV DNA was detected in 6 (12%) SCPs, while KRAS and HRAS mutations were detected in 18 (35%) and 17 (33%) SCPs, respectively. Notably, KRAS mutations, HRAS mutations and HPV infection were mutually exclusive. The larynx and trachea (4/7, 57%) were more preferentially infected by HPV than the other sites (2/44, 5%, p = 0.0019) and HPV was associated with multifocal development (4/5, 80%). In contrast, KRAS and HRAS mutations in SCPs were evenly distributed across the anatomical sites and found only in single SCPs. In conclusion, this study demonstrated that HPV was not frequently involved in SCPs and that RAS mutations were more common alterations. In contrast to inverted sinonasal papillomas and oncocytic sinonasal papillomas, SCP may not be a precursor lesion of carcinoma, because these aetiological events in SCP are distinct from squamous cell carcinoma in the same sites. John Wiley & Sons, Inc. 2020-01-20 /pmc/articles/PMC7164371/ /pubmed/31960612 http://dx.doi.org/10.1002/cjp2.157 Text en © 2020 The Authors. The Journal of Pathology: Clinical Research published by The Pathological Society of Great Britain and Ireland and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Sasaki, Eiichi Masago, Katsuhiro Fujita, Shiro Hanai, Nobuhiro Yatabe, Yasushi Frequent KRAS and HRAS mutations in squamous cell papillomas of the head and neck |
title | Frequent KRAS and HRAS mutations in squamous cell papillomas of the head and neck |
title_full | Frequent KRAS and HRAS mutations in squamous cell papillomas of the head and neck |
title_fullStr | Frequent KRAS and HRAS mutations in squamous cell papillomas of the head and neck |
title_full_unstemmed | Frequent KRAS and HRAS mutations in squamous cell papillomas of the head and neck |
title_short | Frequent KRAS and HRAS mutations in squamous cell papillomas of the head and neck |
title_sort | frequent kras and hras mutations in squamous cell papillomas of the head and neck |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7164371/ https://www.ncbi.nlm.nih.gov/pubmed/31960612 http://dx.doi.org/10.1002/cjp2.157 |
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