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dc.contributor.authorBroumandi, Omid
dc.date.accessioned2023-11-06T08:29:45Z
dc.date.available2023-11-06T08:29:45Z
dc.date.issued2023en_US
dc.identifier.urihttps://dspace.tbzmed.ac.ir:443/xmlui/handle/123456789/69724
dc.description.abstractRecently, various studies have focused on the therapeutic potential of miRNAs, especially miR-100, which is one of the tumor suppressor miRNAs, in various human malignancies, including osteosarcoma. However, the underlying mechanisms in miR-100-mediated anticancer effects are still not fully understood. Therefore, the present study investigated the effect of miR-100 on methotrexate (MTX)-induced apoptosis in MG-63 cells. Methods: MG-63 were treated with MTX, miR-100 and a combination of both, and cell viability was evaluated by MTT method. The expression of miR-100, tetrahydrofolate reductase was evaluated using quantitative real-time polymerase chain reaction (qRT-PCR). Flow cytometry method was also used to investigate apoptosis. Results: Overexpression of miRNA-205 was shown to significantly inhibit the viability of MG-63 cells. Overexpression of miR-100 led to decrease Tetrahydrofolate reductase expression. Also, overexpression of miR-100 increased the apoptosis rate of MG-63 cells.en_US
dc.language.isofaen_US
dc.publisherTabriz University of Medical Sciences, Faculty of Medicineen_US
dc.relation.isversionofhttps://dspace.tbzmed.ac.ir:443/xmlui/handle/123456789/69723en_US
dc.subjectosteosarcomaen_US
dc.subjectmiR-100en_US
dc.subjectapoptosisen_US
dc.subjectMTXen_US
dc.titleThe role of miR-100 in methotrexate resistance in MG-63 osteosarcoma cell lineen_US
dc.typeThesisen_US
dc.contributor.supervisorBazavar, Mohamadreza
dc.contributor.supervisorYousefi, Bahman
dc.identifier.docno6011296en_US
dc.identifier.callno11296en_US
dc.description.disciplineMedicineen_US
dc.description.degreeMD Degreeen_US


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