Polyomaviruses detectable in head and neck carcinomas

dc.contributor.authorSyrjänen S.
dc.contributor.authorPoluschkin L.
dc.contributor.authorRautava J.
dc.contributor.authorTurunen A.
dc.contributor.authorWang Y.
dc.contributor.authorHedman K.
dc.contributor.authorSyrjänen K.
dc.contributor.authorGrenman R.
dc.contributor.organizationfi=hammaslääketieteen laitos|en=Institute of Dentistry|
dc.contributor.organizationfi=korva-, nenä-, ja kurkkutautioppi|en=Otorhinolaryngology - Head and Neck Surgery|
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organization-code1.2.246.10.2458963.20.64787032594
dc.contributor.organization-code2607312
dc.converis.publication-id30819813
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/30819813
dc.date.accessioned2025-08-27T22:52:20Z
dc.date.available2025-08-27T22:52:20Z
dc.description.abstract<p>Polyomaviruses (PyV) independent or jointly with human papillomavirus (HPV), might have a role in head and neck carcinomas (HNSCC). We analyzed the prevalence and viral DNA loads of SV40, JCV and BKV with quantitative PCR (qPCR) and all 13 HPyVs with a novel Multiplex method in 82 HNSCC samples with known HPV status and disease-specific survival (DSS) and 24 HNSCC cell lines.</p><p>JCV was the most prevalent PyV present in 37% of HNSCC and the most prevalent sites were lip (80%), larynx (67%) and oral cavity (59%). JCV viral load was highest in larynx but variation was wide (152514 mean copies/μg DNA, SD± 304820). BKV was found only in one oral carcinoma with low viral load. SV40 was detected in 60% lip and 20.7% oral carcinomas with low copy numbers (6.6- 23.7 copies/μg DNA). Altogether, 86% of JCV-positive samples were co-infected with HPV (p=0.001), with no impact on DSS. Agreement between qPCR and Multiplex methods was substantial (Cohen's kappa= 0.659). Multiplex method detected additional HPyV in five samples. JCV was found in 9/24 HNSCC cell lines, all deriving from oral cavity. Our data provide evidence that JCV might have a role in HNSCC as independent virus or co-factor of HPV.</p>
dc.format.pagerange22642
dc.format.pagerange22652
dc.identifier.jour-issn1949-2553
dc.identifier.olddbid202965
dc.identifier.oldhandle10024/185992
dc.identifier.urihttps://www.utupub.fi/handle/11111/48707
dc.identifier.urnURN:NBN:fi-fe2021042719030
dc.language.isoen
dc.okm.affiliatedauthorRautava, Jaana
dc.okm.affiliatedauthorTurunen, Aaro
dc.okm.affiliatedauthorSyrjänen, Stina
dc.okm.affiliatedauthorGrenman, Reidar
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3122 Cancersen_GB
dc.okm.discipline3125 Otorhinolaryngology, ophthalmologyen_GB
dc.okm.discipline3122 Syöpätauditfi_FI
dc.okm.discipline3125 Korva-, nenä- ja kurkkutaudit, silmätauditfi_FI
dc.okm.internationalcopublicationnot an international co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherImpact Journals LLC
dc.relation.doi10.18632/oncotarget.25202
dc.relation.ispartofjournalOncotarget
dc.relation.issue32
dc.relation.volume9
dc.source.identifierhttps://www.utupub.fi/handle/10024/185992
dc.titlePolyomaviruses detectable in head and neck carcinomas
dc.year.issued2018

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