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dc.contributor.authorAktan, Çağdaş
dc.contributor.authorKüçükaslan, Ali Şahin
dc.contributor.authorCengiz, A. Buğra
dc.contributor.authorDemirci, Mehmet
dc.contributor.authorSunter, Volkan
dc.contributor.authorBaygül, Arzu
dc.contributor.authorDalmızrak, Ayşegül
dc.contributor.authorÜnlü, Özge
dc.contributor.authorYiğit, Özgür
dc.contributor.authorÇakır, Burak Ömür
dc.date.accessioned2023-07-18T11:08:54Z
dc.date.available2023-07-18T11:08:54Z
dc.date.issued2022en_US
dc.identifier.issn2452-0144
dc.identifier.urihttps://doi.org/10.1016/j.genrep.2022.101706
dc.identifier.urihttps://hdl.handle.net/20.500.12462/13224
dc.descriptionDalmızrak, Ayşegül (Balikesir Author)en_US
dc.description.abstractPurpose of the study: lncRNAs appear to act as an important epigenetic regulator of the immune response to bacterial infection in mammals. However, a lncRNA that only exhibits pathogenic or beneficial potential during infection has not yet been described. Moreover, it is still not fully known whether there are specific lncRNAs whose expression changes in response to a particular pathogen or whether lncRNAs are mainly involved in basic cellular immune responses to different stress stimuli. This study aims to assess association between salivary lncRNAs and salivary bacterial pathogens in laryngeal cancer patients. Methods: LINC01206, LINC01209, LINC01994, and ABCC5-AS1 were analyzed among 13 candidate lncRNAs in the saliva samples of 35 patients with laryngeal carcinoma and 25 healthy control. Both their expressions and the quantitative amount of oral bacteria members (Rothia mucilaginosa, Streptococcus spp., Prevotella oris, Veillonella dispar, Neisseria subflava, and Peptostreptococcus stomatis) were analyzed using qPCR. To determine whether these lncRNAs and bacterial pathogens are useful as diagnostic biomarkers, their association with clinicopathological and demographic characteristics was analyzed. Results: When the study group compared with the control group, expression of LINC01206, LINC01209, LINC01994, and ABCC5-AS1 were 2.84-fold, 2.33-fold, 4.46-fold, and 2.27-fold lower, respectively (p < 0.05). In terms of the amount of bacteria DNA in saliva, no significant difference was found between the laryngeal cancer and the control groups (p > 0.05). Conclusion: These results may provide novel insights into the molecular mechanism underlying laryngeal cancer and lncRNA/microbiome applications may constitute a new and alternative method to prevent development of laryngeal cancer in the future.en_US
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.relation.isversionof10.1016/j.genrep.2022.101706en_US
dc.rightsinfo:eu-repo/semantics/embargoedAccessen_US
dc.subjectHead and Neck Canceren_US
dc.subjectLaryngeal Canceren_US
dc.subjectlncRNAen_US
dc.subjectBacteriaen_US
dc.subjectBioinformaticsen_US
dc.titleContext Sensitive Links 1 of 1 Expression of salivary LINC01206, LINC01209, LINC01994, and ABCC5-AS1 may serve as diagnostic tools in laryngeal canceren_US
dc.typearticleen_US
dc.relation.journalGENE Reportsen_US
dc.contributor.departmentTıp Fakültesien_US
dc.contributor.authorID0000-0003-3331-6768en_US
dc.identifier.volume29en_US
dc.identifier.startpage1en_US
dc.identifier.endpage10en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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