Single nucleotide polymorphism rs11614913 associated with CC genotype in miR-196a2 is overrepresented in laryngeal squamous cell carcinoma, but not salivary gland tumors in Polish population

dc.contributor.authorMarcin Skalski
dc.contributor.authorAdam Ustaszewski
dc.contributor.authorKatarzyna Jaskiewicz
dc.contributor.authorKatarzyna Kiwerska
dc.contributor.authorMalgorzata Wierzbicka
dc.contributor.authorHanna Klimza
dc.contributor.authorReidar Grenman
dc.contributor.authorMaciej Giefing
dc.contributor.organizationfi=korva-, nenä-, ja kurkkutautioppi|en=Otorhinolaryngology - Head and Neck Surgery|
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organization-code2607312
dc.converis.publication-id31857854
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/31857854
dc.date.accessioned2022-10-28T12:19:21Z
dc.date.available2022-10-28T12:19:21Z
dc.description.abstractThe miRNA-196a2 has shown significance in the development of various neoplasms, including head and neck squamous cell carcinoma (HNSCC). The oncogenic functionality of this miRNA is mediated via its potential to target annexin A1 mRNA, a tumor suppressor gene involved in inhibition of the NF-kappa B pathway. Interestingly, recent data indicate a susceptibility for aforementioned neoplasms in patients with the CC genotype vs the CT and TT genotypes of the rs11614913 SNP located within the DNA sequence of the miR-196a2 that results in elevated expression of the gene. To further investigate this phenomenon, we genotyped this SNP in 40 patients with laryngeal squamous cell carcinoma (LSCC), the most common tumor of the head and neck region and 60 patients with salivary gland tumors (SGT) that show a yet unexplained incidence increase in the last two decades. In agreement with previous reports, we have identified a statistically significant (p < 0.05) overrepresentation of the CC genotype in LSCC patients and demonstrated in LSCC cell lines that it results in elevated expression of miR-196a2 as compared to cell lines with the TT genotype of the respective SNP. Importantly, none of these correlations was found in patients with SGT. These findings underline the importance of the SNP rs11614913 for LSCC development in the Polish population and moreover highlight the different genetic background of the two studied neoplasms of the head and neck region.
dc.format.pagerange301
dc.format.pagerange304
dc.identifier.eissn2190-3883
dc.identifier.jour-issn2190-3883
dc.identifier.olddbid175828
dc.identifier.oldhandle10024/158922
dc.identifier.urihttps://www.utupub.fi/handle/11111/29447
dc.identifier.urnURN:NBN:fi-fe2021042719273
dc.language.isoen
dc.okm.affiliatedauthorGrenman, Reidar
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3122 Cancersen_GB
dc.okm.discipline3122 Syöpätauditfi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherSPRINGER HEIDELBERG
dc.publisher.countryGermanyen_GB
dc.publisher.countrySaksafi_FI
dc.publisher.country-codeDE
dc.relation.doi10.1007/s13353-018-0445-6
dc.relation.ispartofjournalJournal of Applied Genetics
dc.relation.issue3
dc.relation.volume59
dc.source.identifierhttps://www.utupub.fi/handle/10024/158922
dc.titleSingle nucleotide polymorphism rs11614913 associated with CC genotype in miR-196a2 is overrepresented in laryngeal squamous cell carcinoma, but not salivary gland tumors in Polish population
dc.year.issued2018

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