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ID 117725
Author
Ikegami, Taro University of the Ryukyus
Kise, Norimoto University of the Ryukyus
Kinjyo, Hidetoshi University of the Ryukyus
Kondo, Shunsuke University of the Ryukyus
Suzuki, Mikio University of the Ryukyus
Tsukahara, Narutoshi University of the Ryukyus
Kiyuna, Asanori University of the Ryukyus
Agena, Shinya University of the Ryukyus
Tanaka, Katsunori University of the Ryukyus
Hasegawa, Narumi University of the Ryukyus
Kawakami, Junko University of the Ryukyus
Ganaha, Akira University of Miyazaki
Maeda, Hiroyuki University of the Ryukyus
Hirakawa, Hitoshi University of the Ryukyus
Keywords
laryngeal papilloma
human papillomavirus 6
human papillomavirus 11
viral DNA and mRNA expression
anti-E4 antibody
Content Type
Journal Article
Description
Laryngeal papilloma (LP), which is associated with infection by human papillomavirus (HPV)-6 or -11, displays aggressive growth. The precise molecular mechanism underlying the tumorigenesis of LP has yet to be uncovered. Building on our earlier research into HPV-6, in this study, the viral gene expression of HPV-11 was investigated by quantitative PCR and DNA/RNA in situ hybridization. Additionally, newly developed antibodies against the E4 protein of HPV-6 and HPV-11 were evaluated by immunohistochemistry. The average viral load of HPV-11 in LP was 1.95 ± 0.66 × 105 copies/ng DNA, and 88% of HPV mRNA expression was found to be E4, E5a, and E5b mRNAs. According to RNA in situ hybridization, E4 and E5b mRNAs were expressed from the middle to upper part of the epithelium. E4 immunohistochemistry revealed a wide positive reaction in the upper cell layer in line with E4 mRNA expression. Other head and neck lesions with HPV-11 infection also showed a positive reaction in E4 immunohistochemistry. The distribution pattern of HPV DNA, viral mRNA, and E4 protein in LP with HPV-11 infection was quite similar to that of HPV-6. Therefore, it might be possible to apply these E4-specific antibodies in other functional studies as well as clinical applications, including targeted molecular therapies in patients with HPV-6 and HPV-11 infection.
Journal Title
Viruses
ISSN
19994915
Publisher
MDPI
Volume
13
Issue
10
Start Page
2024
Published Date
2021-10-07
Rights
This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
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language
eng
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departments
Oral Sciences