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dc.contributor.authorIzgi, Ahu
dc.contributor.authorGunal, Armagan
dc.contributor.authorYalcin, Serap
dc.contributor.authorGunduz, Ufuk
dc.date.accessioned2019-11-24T20:59:02Z
dc.date.available2019-11-24T20:59:02Z
dc.date.issued2014
dc.identifier.issn0753-3322
dc.identifier.issn1950-6007
dc.identifier.urihttps://dx.doi.org/10.1016/j.biopha.2014.08.014
dc.identifier.urihttps://hdl.handle.net/20.500.12513/3204
dc.descriptionWOS: 000345001400004en_US
dc.descriptionPubMed ID: 25194444en_US
dc.description.abstractThe ends of chromosoms, telomeres are bound with a number of proteins which protect and stabilize telomeres against degredation, end to end fusion and aberrant recombinations. Telomeric DNA is bound of two groups of proteins, which are double-stranded telomeric DNA bindings proteins, and single stranded telomeric binding proteins. Among telomere binding proteins, protections of telomere 1 protein is a single stranded telomere binding proteins and suggested to be a significant player for telomere elongation and has an association with an enzyme called as telomerase which is an intrinsic reverse transcriptase. Telomerase synthesizes hexameric telomeric repeats onto the chromosomes thereby compansating telomere loss in immortal cells, such as tumor cells, whereas telomeres are shorthened with each division in normal cells. PCR-based TRAP (telomeric repeat amplification protocol) assay is a very sensitive assay for the detection of enzymatic activity of telomerase even if a few numbers of cancerous cells are available. The association between telomerase activity and hPOT1 expression in colorectal cancer is still unclear. Protein extraction was performed from specimens of matched normal and colorectal cancer specimens. Protein concentrations were determined by Bradford assay. Optimized protein concentrations were used for TRAP Assay. TRAP products were seperated by vertical gel electrophoresis on 12.5% polyacrylamide gels and visualized by silver staining. Gene expression of hPOT1 was determined by qPCR analysis. The results demonstrated that all tumor tissues were telomerase positive whereas all corresponding normal tissue was telomerase negative. Among clinicopathological findings, telomerase activity was found to be associated with stage, histology, localization, distant metastasis and lymph node metastasis of tumor in the current study. Although all of the clinicopathological findings differed in the expression of hPOT1 compared to normal tissues, they did not differ from each other significantly, except side of tumor and lymph node metastasis. Telomerase activity and hPOT1 gene expression may serve as a promising tumor marker for colorectal cancer and there is a close association between the enzymatic activty of telomerase and the expression of human protection of telomere 1 gene. (C) 2014 Elsevier Masson SAS. All rights reserved.en_US
dc.language.isoengen_US
dc.publisherELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIERen_US
dc.relation.isversionof10.1016/j.biopha.2014.08.014en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectTelomerase activityen_US
dc.subjectColorectal canceren_US
dc.subjecthPOT1en_US
dc.subjectTRAP assayen_US
dc.titleTelomere 1 (POT1) gene expression and its association with telomerase activity in colorectal tumor samples with different pathological featuresen_US
dc.typearticleen_US
dc.relation.journalBIOMEDICINE & PHARMACOTHERAPYen_US
dc.contributor.departmentKırşehir Ahi Evran Üniversitesi, Mühendislik-Mimarlık Fakültesi, Gıda Mühendisliği Bölümüen_US
dc.identifier.volume68en_US
dc.identifier.issue7en_US
dc.identifier.startpage841en_US
dc.identifier.endpage846en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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