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dc.contributor.authorCelik, Betul
dc.contributor.authorPasin, Ozge
dc.contributor.authorSen, Sena
dc.contributor.authorTuncer, Seref Bugra
dc.contributor.authorKayim, Zubeyde Yalniz
dc.contributor.authorErciyas, Seda Kilic
dc.contributor.authorErdogan, Ozge Sukruoglu
dc.contributor.authorGultaslar, Busra Kurt
dc.contributor.authorGhafour, Arash Adamnejad
dc.contributor.authorYazici, Hulya
dc.contributor.authorOlgac, Necat Vakur
dc.date.accessioned2023-11-07T06:15:09Z
dc.date.available2023-11-07T06:15:09Z
dc.date.issued2023en_US
dc.identifier.citationCelik, B., Pasin, O., Sen, S., Tuncer, S. B., Kayım, Z. Y., Erciyas, S. K., ... & Olgac, N. V. (2023). DNA methylation of KIFC1 gene in determination of histological diagnosis, prognosis and metastasis of lung cancer. Pathology-Research and Practice, 249, 154742.en_US
dc.identifier.issn03440338
dc.identifier.urihttps://doi.org/10.1016/j.prp.2023.154742
dc.identifier.urihttps://hdl.handle.net/20.500.12294/3961
dc.description.abstractBackground: One of the main features of cancer, especially lung cancer (LC), is abnormal cell division. Abnormal expression of kinesin family member C1 (KIFC1/HSET), which is involved in mitotic cell division and ensures equatorial alignment of chromosomes during division, is observed in both premalignant and malignant lesions. There are no studies in the literature addressing the role of KIFC1 in the diagnosis and follow-up of LC. In this study, we investigated the epigenetic role of KIFC1 in the diagnosis, stage, and prognosis of various histological subtypes diagnosed with LC. Material and Methods: The expression and methylation status of the KIFC1 gene were examined after DNA/RNA isolation in tumor, conjugate normal tissue, and blood samples from 39 patients diagnosed with LC and in blood samples from 39 healthy controls. Changes in KIFC1 gene expression were examined by the Quantitative Real Time-PCR (qRT-PCR) method after cDNA synthesis following RNA isolation. The Methylation-Specific PCR (MSP) method was used to determine the methylation status of the KIFC1 gene. In this study, the expression/methylation profiles of the KIFC1 gene and the clinical and pathological characteristics of the patients were analyzed by statistical methods. Result: Hypomethylation was detected in 95.8% of the 62.1% of patients’ tissues with increased KIFC1 gene expression. The expression level of the KIFC1 gene was found to be increased 3.2-fold in the tumor tissues of the patients compared with the conjugated normal tissues and 2.4-fold in the serum of the patients compared with the healthy serum. Statistical comparison of patients' clinical parameters and methylation and expression results revealed statistical significance between KIFC1 expression and metastasis, tumor stage and tumor grade. Conclusion: In conclusion, the increase in the expression level of the KIFC1 gene is higher in patients diagnosed with LC than in the healthy population, and therefore, the increase in the expression level of the KIFC1 gene due to hypomethylation can be used as a screening biomarker in LC. It can also be considered that the methylation profile of the KIFC1 gene may be a potential biomarker for determining the subtype of squamous cell carcinoma in LC. The results of the study need to be analyzed and continued with a larger number of patients. © 2023 Elsevier GmbHen_US
dc.language.isoengen_US
dc.publisherELSEVIER GMBHen_US
dc.relation.ispartofPATHOLOGY RESEARCH AND PRACTICEen_US
dc.identifier.doi10.1016/j.prp.2023.154742en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectBiomarkeren_US
dc.subjectExpressionen_US
dc.subjectKIFC1en_US
dc.subjectLung Canceren_US
dc.subjectMethylationen_US
dc.titleDNA methylation of KIFC1 gene in determination of histological diagnosis, prognosis and metastasis of lung canceren_US
dc.typearticleen_US
dc.departmentTıp Fakültesi, Temel Tıp Bilimleri Bölümüen_US
dc.authorid0000-0002-8919-0482en_US
dc.identifier.volume249en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.institutionauthorYazici, Hulya
dc.authorwosidGSK-8744-2022en_US
dc.authorscopusid7102511789en_US
dc.identifier.wosqualityQ2en_US
dc.identifier.wosWOS:001071621100001en_US
dc.identifier.scopus2-s2.0-85169605295en_US
dc.identifier.pmid37666088en_US


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