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dc.contributor.authorÜnlü, Özge
dc.contributor.authorDemirci, Mehmet
dc.contributor.authorPaksoy, Tuğçe
dc.contributor.authorEden, Arzu Baygül
dc.contributor.authorTansuker, Hasan Deniz
dc.contributor.authorDalmIzrak, Ayşegül
dc.contributor.authorAktan, Çağdaş
dc.contributor.authorŞenel, Firdevs
dc.contributor.authorSünter, Ahmet Volkan
dc.contributor.authorYiğit, Özgür
dc.contributor.authorÇakır, Burak Ömür
dc.contributor.authorKantarcı, Alpdoğan
dc.date.accessioned2024-09-04T11:50:49Z
dc.date.available2024-09-04T11:50:49Z
dc.date.issued2024en_US
dc.identifier.citationUnlu, O., Demirci, M., Paksoy, T., Eden, A. B., Tansuker, H. D., Dalmizrak, A., Aktan, C., Senel, F., Sunter, A. V., Yigit, O., Cakir, B. O., & Kantarci, A. (2024). Oral microbial dysbiosis in patients with oral cavity cancers. Clinical Oral Investigations, 28(7). https://doi.org/10.1007/s00784-024-05770-8en_US
dc.identifier.issn1432-6981
dc.identifier.urihttps://hdl.handle.net/20.500.12900/388
dc.description.abstractObjectives The pathogenesis of oral cavity cancers is complex. We tested the hypothesis that oral microbiota dysbiosis is associated with oral cavity cancer. Materials and methods Patients with primary oral cavity cancer who met the inclusion and exclusion criteria were included in the study. Matching healthy individuals were recruited as controls. Data on socio-demographic and behavioral factors, self-reported periodontal measures and habits, and current dental status were collected using a structured questionnaire and periodontal chartings. In addition to self-reported oral health measures, each participant received a standard and detailed clinical examination. DNA was extracted from saliva samples from patients and healthy controls. Next-generation sequencing was performed by targeting V3-V4 gene regions of the 16 S rRNA with subsequent bioinformatic analyses. Results Patients with oral cavity cancers had a lower quality of oral health than healthy controls. Proteobacteria, Aggregatibacter, Haemophilus, and Neisseria decreased, while Firmicutes, Bacteroidetes, Actinobacteria, Lactobacillus, Gemella, and Fusobacteria increased in oral cancer patients. At the species level, C. durum, L. umeaens, N. subflava, A. massiliensis, and V. dispar were significantly lower, while G. haemolysans was significantly increased (p < 0.05). Major periodontopathogens associated with periodontal disease (P. gingivalis and F.nucleatum) increased 6.5- and 2.8-fold, respectively. Conclusion These data suggested that patients with oral cancer had worse oral health conditions and a distinct oral microbiome composition that is affected by personal daily habits and may be associated with the pathogenicity of the disease and interspecies interactions. Clinical relevance This paper demonstrates the link between oral bacteria and oral cancers, identifying mechanistic interactions between species of oral microbiome.en_US
dc.language.isoengen_US
dc.publisherSPRINGER HEIDELBERGen_US
dc.relation.isversionof10.1007/s00784-024-05770-8en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectOral cavity cancersen_US
dc.subjectOral microbiotaen_US
dc.subjectSalivaen_US
dc.subjectPeriodontal diseaseen_US
dc.titleOral microbial dysbiosis in patients with oral cavity cancersen_US
dc.typearticleen_US
dc.departmentİstanbul Atlas Üniversitesi, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümüen_US
dc.authoridhttps://orcid.org/0000-0002-5411-5925en_US
dc.contributor.institutionauthorÜnlü, Özge
dc.identifier.volume28en_US
dc.identifier.issue7en_US
dc.relation.journalCLINICAL ORAL INVESTIGATIONSen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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