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dc.contributor.authorOzcan, Onder
dc.contributor.authorBelli, Ahmet Korkut
dc.contributor.authorKayilloglu, Selami Ilgaz
dc.contributor.authorDonmez, Cem
dc.contributor.authorCelik, Ozgur Ilhan
dc.contributor.authorKaplan, Mehmet
dc.contributor.authorPolat, Murat
dc.date.accessioned2020-11-20T14:42:03Z
dc.date.available2020-11-20T14:42:03Z
dc.date.issued2019
dc.identifier.issn1309-0720
dc.identifier.issn1309-2014
dc.identifier.urihttps://doi.org/10.4328/JCAM.6099
dc.identifier.urihttps://hdl.handle.net/20.500.12809/1019
dc.descriptionOzcan, Onder/0000-0001-8252-3339en_US
dc.descriptionWOS: 000475294300004en_US
dc.description.abstractAim: Many genes have been identified to control cell proliferation in human such as RUNX gene family. Mutations in these genes have been shown to be responsible for various cancer developments. Our aim in this study is to Investigate RUNX gene family expressions in breast cancer and breast fibroadenomas. Material and Method: All consecutive patients whose histopathological examination resulted in breast cancer, fibroadenoma, or normal breast tissue between the years 2012 and 2014 were included in the study. Total RNA from each sample was isolated with genomic RNA extraction sample and gene expressions of RUNX1, RUNX2, and RUNX3 were measured with real- time polymerase chain reaction. Gene expressions and patients' characteristics were evaluated among histopathological groups. Results: According to statistical analysis, RUNX1 and RUNX2 expressions were upregulated in fibroadenoma patients while only RUNX2 expression was found to be upregulated in breast cancer patients. RUNX1 was upregulated in patients with p53 mutation, whereas RUNX2 was upregulated in patients without p53 mutation. Discussion: To the best of our knowledge, our study is the first study that evaluates RUNX1, RUNX2, and RUNX3 gene expressions in both benign and malignant breast disease. RUNX2 gene was significantly upregulated in patients with both breast cancer and fibroadenoma in our study. In contrast, however, upregulated, RUNX1 and RUNX3 gene upregulations in the breast cancer and fibroadenoma patients were not statistically significant. In our study, RUNX2 may be a good prognostic factor in contrast to its role in osteosarcoma or bone metastasis in breast and prostate cancer.en_US
dc.item-language.isoengen_US
dc.publisherDerman Medical Publen_US
dc.item-rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectBreast Canceren_US
dc.subjectFibroadenomaen_US
dc.subjectRUNX1 Geneen_US
dc.subjectRUNX2 Geneen_US
dc.subjectRUNX3 Geneen_US
dc.titleRUNX genes expressions in breast cancer and fibroadenomaen_US
dc.item-typearticleen_US
dc.contributor.departmenten_US
dc.contributor.departmentTemp[Ozcan, Onder; Belli, Ahmet Korkut; Kayilloglu, Selami Ilgaz; Donmez, Cem; Polat, Murat] Mugla Sitki Kocman Univ, Sch Med, Dept Gen Surg, TR-48000 Mugla, Turkey -- [Celik, Ozgur Ilhan] Mugla Sitki Kocman Univ, Dept Pathol, Med Sch, Mugla, Turkey -- [Kaplan, Mehmet] NCR Int Hosp, Dept Gen Surg, Gaziantep, Turkeyen_US
dc.identifier.doi10.4328/JCAM.6099
dc.identifier.volume10en_US
dc.identifier.issue3en_US
dc.identifier.startpage316en_US
dc.identifier.endpage319en_US
dc.relation.journalJournal of Clinical and Analytical Medicineen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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