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dc.contributor.authorTunçer, Şeref Buğraen_US
dc.contributor.authorÇelik, Betülen_US
dc.contributor.authorAkdeniz Ödemiş, Demeten_US
dc.contributor.authorKılıç Erciyas, Sedaen_US
dc.contributor.authorŞükrüoğlu Erdoğan, Özgeen_US
dc.contributor.authorAvşar, Mukaddesen_US
dc.contributor.authorKuru Türkcan, Gözdeen_US
dc.contributor.authorYazıcı, Hülyaen_US
dc.date.accessioned2022-02-21T08:50:10Z
dc.date.available2022-02-21T08:50:10Z
dc.date.issued2022en_US
dc.identifier.citationTuncer, S. B., Celik, B., Akdeniz Odemis, D., Kılıc Erciyas, S., Sukruoglu Erdogan, O., Avsar, M., . . . Yazici, H. (2022). miRNA sequence analysis in patients with Kaposi’s sarcoma-associated herpesvirus. Pathology and Oncology Research, 28 doi:10.3389/pore.2022.1610055en_US
dc.identifier.issn12194956
dc.identifier.urihttps://doi.org/10.3389/pore.2022.1610055
dc.identifier.urihttps://hdl.handle.net/20.500.12294/2981
dc.description.abstractMicroRNAs (miRNAs) are the non-coding RNAs that can both attach to the untranslated and coding sections of target mRNAs, triggering destruction or post-transcriptional alteration. miRNAs regulate various cellular processes such as immune function, apoptosis, and tumorigenesis. About 35,000 miRNAs have been discovered in the human genome. The increasing evidence suggests that the dysregulation of human miRNAs may have a role in the etiology of some disorders including cancer. Only a small sub-set of human miRNAs has functionally been validated in the pathogenesis of oncogenic viruses such as Kaposi’s sarcoma-associated herpesvirus (KSHV). KSHV is the cause of various human malignancies including primary effusion lymphoma (PEL) and Kaposi’s sarcoma (KS), which are mainly seen in AIDS patients or other immunocompromised people. We aimed to identify the miRNAs in Kaposi’s sarcoma cases, with the comparison of KSHV seropositive and seronegative tumors with the controls and in each other in Turkish Kaposi’s sarcoma patients. We performed the miRNA-sequencing at genome level in the peripheral blood mononuclear cells of 16 Kaposi’s sarcoma patients, and in 8 healthy controls matched for age, gender, and ethnicity. A total of 642 miRNA molecules with different expression profiles were identified between the patients and the healthy controls. Currently, out of 642 miRNAs, 7 miRNAs (miR-92b-3p, miR-490-3p, miR-615-3p, miR-629-5p, miR-1908, miR-3180, miR-4433b-3p) which have not been described in the literature in the context of Kaposi’s sarcoma were addressed in the study for the first time and 9 novel miRNAs, not found previously in the database, have been detected in Kaposi’s sarcoma using the miRNA-sequencing technique. This study demonstrates the identification of differently expressed miRNAs which might be the new therapeutic targets for Kaposi’s sarcoma, that has limited treatment options and can be used in the etiology, diagnosis, and prognosis of this cancer.en_US
dc.language.isoengen_US
dc.publisherFrontiers Media S.A.en_US
dc.relation.ispartofPathology and Oncology Researchen_US
dc.identifier.doi10.3389/pore.2022.1610055en_US
dc.identifier.doi10.3389/pore.2022.1610055
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.rightsAttribution-NoDerivs 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nd/3.0/us/*
dc.subjectKaposi’s Sarcomaen_US
dc.subjectKSHVen_US
dc.subjectmiRNA-seqen_US
dc.subjectPrognosisen_US
dc.subjectVirusen_US
dc.titlemiRNA Sequence Analysis in Patients With Kaposi's Sarcoma-Associated Herpesvirusen_US
dc.typearticleen_US
dc.departmentTıp Fakültesi, Temel Tıp Bilimleri Bölümüen_US
dc.identifier.volume28en_US
dc.identifier.startpage1en_US
dc.identifier.endpage10en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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