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Mapping human papillomavirus, Epstein–Barr virus, cytomegalovirus, adenovirus, and p16 in laryngeal cancer
Umeå University, Faculty of Medicine, Department of Clinical Sciences, Otorhinolaryngology. ÖNH-Kliniken, Östersunds Sjukhus, Umeå University, Östersund, Sweden.ORCID iD: 0000-0003-0007-8716
Umeå University, Faculty of Medicine, Department of Clinical Sciences, Otorhinolaryngology. ÖNH-Kliniken, Östersunds Sjukhus, Umeå University, Östersund, Sweden.ORCID iD: 0000-0003-3522-1842
Umeå University, Faculty of Medicine, Department of Medical Biosciences, Pathology.ORCID iD: 0000-0002-4831-4100
Umeå University, Faculty of Medicine, Department of Clinical Microbiology, Section of Virology.ORCID iD: 0000-0001-6949-1213
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2022 (English)In: Discover Oncology, E-ISSN 2730-6011, Vol. 13, no 1, article id 18Article in journal (Refereed) Published
Abstract [en]

Purpose: Apart from tobacco and alcohol, viral infections are proposed as risk factors for laryngeal cancer. The occurrence of oncogenic viruses including human papilloma virus (HPV) and Epstein–Barr virus (EBV), in laryngeal squamous cell carcinoma (LSCC) varies in the world. Carcinogenesis is a multi-step process, and the role of viruses in LSCC progression has not been clarified. We aimed to analyze the presence and co-expression of HPV, EBV, human cytomegalovirus (HCMV) and human adenovirus (HAdV) in LSCC. We also investigated if p16 can act as surrogate marker for HPV in LSCC.

Methods: Combined PCR/microarrays (PapilloCheck®) were used for detection and genotyping of HPV DNA, real-time PCR for EBV, HCMV and HAdV DNA detection, and EBER in situ hybridization (EBER-ISH) for EBV detection in tissue from 78 LSCC patients. Additionally, we analyzed p16 expression with immunohistochemistry.

Results: Thirty-three percent (26/78) of LSCC tumor samples were EBV positive, 9% (7/78) HCMV positive and 4% (3/78) HAdV positive. Due to DNA fragmentation, 45 samples could not be analyzed with PapilloCheck®; 9% of the remaining (3/33) were high-risk HPV16 positive and also over-expressed p16. A total of 14% (11/78) of the samples over-expressed p16.

Conclusion: These findings present a mapping of HPV, EBV, HCMV and HAdV, including the HPV surrogate marker p16, in LSCC in this cohort. Except for EBV, which was detected in a third of the samples, data show viral infection to be uncommon, and that p16 does not appear to be a specific surrogate marker for high-risk HPV infection in LSCC.

Place, publisher, year, edition, pages
Springer, 2022. Vol. 13, no 1, article id 18
National Category
Cancer and Oncology Otorhinolaryngology
Research subject
Oncology
Identifiers
URN: urn:nbn:se:umu:diva-193581DOI: 10.1007/s12672-022-00475-4ISI: 000771496000002PubMedID: 35312853Scopus ID: 2-s2.0-85126886934OAI: oai:DiVA.org:umu-193581DiVA, id: diva2:1652384
Available from: 2022-04-19 Created: 2022-04-19 Last updated: 2022-10-12Bibliographically approved
In thesis
1. Mapping viruses in non-malignant tonsils, nasal polyps, sinonasal inverted papilloma and laryngeal cancer
Open this publication in new window or tab >>Mapping viruses in non-malignant tonsils, nasal polyps, sinonasal inverted papilloma and laryngeal cancer
2022 (English)Doctoral thesis, comprehensive summary (Other academic)
Alternative title[sv]
Kartläggning av virus i godartade halsmandlar, näspolyper och inverterat papillom i näsa-bihålor samt cancer i struphuvudet
Abstract [en]

Background: The upper respiratory tract is exposed to viruses, which can lead to infection and cancer development. We chose to study common and/or chronic diseases along with common and cancer related viruses in the upper airway. High-risk human papillomavirus (HPV) causes cancer in tonsils and base of tongue, and Epstein-Barr virus (EBV) in the nasopharynx. p16 is used as a site-specific tumor marker for HPV. Human cytomegalovirus (HCMV) and human adenovirus (HAdV) are proposed to be oncomodulatory. It is unclear what significance these viruses have in benign tonsillar disease, chronic rhinosinusitis with nasal polyps (CRSwNP), sinonasal inverted papillomas (SIP) and laryngeal squamous cell carcinoma (LSCC). If virus is identified, it could make possible the use of current vaccines in prevention and treatment, as well as protection of healthcare providers.

Material and Methods: We analyzed 40 benign tonsils, 45 paired nasal polyp and healthy nasal mucosa samples, 53 SIP and 78 LSCC samples. We used PCR/microarrays (PapilloCheck®) for HPV detection and genotyping, immunohistochemistry (IHC) for p16 expression and real-time PCR for EBV, HCMV and HAdV detection. Additionally, Epstein-Barr encoding region (EBER) in situ hybridization (ISH) was used for EBV localization and count.

Results: HPV and p16 were not co-expressed, and p16 levels were low in benign tonsils, nasal polyps, and paired controls. Also, 9% of LSCC samples were high-risk HPV 16 positive and over-expressed p16.

EBV-positive cells were detected in 65% of the tonsils, nasal polyps (36%) versus controls (12%), 30% of SIP cases and 33% of LSCC samples.

Conclusions: EBV is commonly identified in benign tonsils, nasal polyps, SIP and LSCC, when using sensitive and robust detection methods. At the same time, viral infection with HPV, HCMV or HAdV appears to be uncommon in these conditions. p16 does not emerge as a reliable marker for HPV infection in LSCC.

Place, publisher, year, edition, pages
Umeå: Umeå University, 2022. p. 72
Series
Umeå University medical dissertations, ISSN 0346-6612 ; 2188
Keywords
Human papilloma virus, Epstein-Barr virus, Human cytomegalovirus, Human adenovirus, p16 tumor suppressor protein, Non-malignant tonsillar disease, Chronic rhino sinusitis with nasal polyps, sinonasal inverted papilloma, laryngeal cancer, EBER-ISH
National Category
Otorhinolaryngology
Research subject
Oto-Rhino-Laryngology
Identifiers
urn:nbn:se:umu:diva-200180 (URN)978-91-7855-841-4 (ISBN)978-91-7855-842-1 (ISBN)
Public defence
2022-11-25, Hörsalen Snäckan, Hus 16, Östersunds Sjukhus, Östersunds sjukhus, Kyrkgatan 16, Östersund, 09:00 (Swedish)
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Available from: 2022-11-04 Created: 2022-10-12 Last updated: 2022-10-13Bibliographically approved

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Schindele, AlexandraHolm, AnnaNylander, KarinAllard, AnnikaOlofsson, Katarina

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