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dc.contributor.authorKaraman, Musa
dc.contributor.authorYıldırım, Hatice
dc.contributor.authorKöçkar, Feray
dc.date.accessioned2019-10-17T07:36:56Z
dc.date.available2019-10-17T07:36:56Z
dc.date.issued2015en_US
dc.identifier.issn1742-464X
dc.identifier.issn1742-4658
dc.identifier.urihttps://hdl.handle.net/20.500.12462/7660
dc.description.abstractCarbonic anhydrases (CAs) (EC 4.2.1.1) are zinc-containing met-alloenzymes that catalyze the hydration of CO2molecule anddehydration of HCO3-ions. Carbonic anhydrase 9 is expressed inmany solid tumors and plays a significant role in tumor acid-base homeostasis. Depletion of CA9 gene expression or inhibition ofits catalytic activity shown to retard tumor growth in murinemodels and reduce metastasis.Tetraspanins are integral mem-brane proteins playing a role as organizers of multimolecularcomplexes in the plasma membrane. The human tumor-associ-ated antigen CO-029 (TSPAN8) is a monoclonal antibody-defined cell surface glycoprotein and described as metastasis-pro-moting in several tumor systems. In this study, we aimed to eval-uate the effects of silencing genes, CA9, and TSPAN8, on theinvasion properties of human pancreatic carcinoma (Panc1) cells.Therefore, cells were transfected with specific siRNAs with siR-NA transfection method along with control siRNAs for non-spe-cific targets. Upon silencing, mRNA and protein assays showthat the expression of CAIX and TSPAN8 were decreased com-pared to control cells. siRNA transfected cells were subjected tocell cytotoxicity assay at different time points in order to see ifthe silencing result in an proliferative effect. In addition, the met-astatic and proliferative profiles of CAIX and TSPAN8 weredetermined after in order to 72 and 92 hours by matrigel and clo-nogenic assay.en_US
dc.language.isoengen_US
dc.publisherWiley-Blackwellen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.titleSilencing of carbonic anhydrase 9 and tetraspanin-8 caused decrease at invasion capacity of human pancreatic carcinoma (PANC-1) cellsen_US
dc.typeotheren_US
dc.relation.journalFebs Journalen_US
dc.contributor.departmentFen Edebiyat Fakültesien_US
dc.identifier.volume282en_US
dc.identifier.issue1en_US
dc.identifier.startpage226en_US
dc.identifier.endpage226en_US
dc.relation.publicationcategoryDiğeren_US


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