2021
DOI: 10.1016/j.oraloncology.2020.105109
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Human papillomavirus genotype distribution in head and neck cancer: Informing developing strategies for cancer prevention, diagnosis, treatment and surveillance

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Cited by 20 publications
(23 citation statements)
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“…HPV 44 belongs to a mucosotropic group of HPVs found in benign and malignant lesions of the anogenital tract and fortuitously in tissues and lesions of the oral cavity, oropharynx, and esophagus [ 27 ]. A number of samples in our study contained more than one HPV type, which is in line with some [ 32 , 35 , 42 , 43 , 44 , 57 , 65 ] but not all studies [ 33 ].…”
Section: Discussionsupporting
confidence: 88%
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“…HPV 44 belongs to a mucosotropic group of HPVs found in benign and malignant lesions of the anogenital tract and fortuitously in tissues and lesions of the oral cavity, oropharynx, and esophagus [ 27 ]. A number of samples in our study contained more than one HPV type, which is in line with some [ 32 , 35 , 42 , 43 , 44 , 57 , 65 ] but not all studies [ 33 ].…”
Section: Discussionsupporting
confidence: 88%
“…Our results support the epidemiological evidence that some head and neck cancers are caused by HPV and that the main risk factors of HNSCC are tobacco and alcohol abuse [1]. The overall prevalence of HPV in the HNSCC group was 42.1%, which is in line with a large number of reports of HPV DNA (2.4-74%) in head and neck cancer patients [8,[31][32][33]40,[50][51][52][53][54][55][56][57][58][59]. The data concerning HPV infection in HNSCC patients in Poland are very inconclusive.…”
Section: Hpv Infection In Hnsccsupporting
confidence: 90%
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“…In parallel, we implemented a bioinformatics-based approach to define local specificity of potential amplicon regions by comparing the HPV16 and HPV18 genomes. We chose these two genomes as they represent the highest and second highest HPV types in HPV+ cancers [ 29 ], respectively. We chose to use an 80 nucleotide sliding window to approximate the size of a small primer-probe amplicon-based assay (2 × 25 nt primers + 30 nt probe), given that most abundant cell free DNA expected to be accessible to standard ddPCR assay-design is in the range of 73–165 nts [ 30 ].…”
Section: Resultsmentioning
confidence: 99%