نمایش مختصر رکورد

dc.contributor.authorSuardi, Rahmaen_US
dc.contributor.authorYsrafil, Ysrafilen_US
dc.contributor.authorSesotyosari, Salsabilaen_US
dc.contributor.authorMartien, Ronnyen_US
dc.contributor.authorWardana, Tirtaen_US
dc.contributor.authorAstuti, Indwianien_US
dc.contributor.authorHaryana, Sofiaen_US
dc.date.accessioned1399-07-22T18:19:58Zfa_IR
dc.date.accessioned2020-10-13T18:19:59Z
dc.date.available1399-07-22T18:19:58Zfa_IR
dc.date.available2020-10-13T18:19:59Z
dc.date.issued2020-09-01en_US
dc.date.issued1399-06-11fa_IR
dc.date.submitted2020-01-07en_US
dc.date.submitted1398-10-17fa_IR
dc.identifier.citationSuardi, Rahma, Ysrafil, Ysrafil, Sesotyosari, Salsabila, Martien, Ronny, Wardana, Tirta, Astuti, Indwiani, Haryana, Sofia. (2020). The Effects of Combination of Mimic miR-155-5p and Antagonist miR-324-5p Encapsulated Chitosan in Ovarian Cancer SKOV3. Asian Pacific Journal of Cancer Prevention, 21(9), 2603-2608. doi: 10.31557/APJCP.2020.21.9.2603en_US
dc.identifier.issn1513-7368
dc.identifier.issn2476-762X
dc.identifier.urihttps://dx.doi.org/10.31557/APJCP.2020.21.9.2603
dc.identifier.urihttp://journal.waocp.org/article_89261.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/434744
dc.description.abstractObjective: Ovarian cancer is a malignant tumor that attacks reproductive organs of women. MicroRNA is known to have an involvement in the prognosis of ovarian cancer. One of them is miR-155-5p which is down regulated and miR-324-5p which is up regulated. Chitosan is used as microRNA delivery system. The aims of this study is to find out the effects of combination microRNA encapsulated chitosan in cell line SKOV3. Methods: Cell line SKOV3 obtained from Stem Cell and Cancer Institute (Kalbe). Mimic miR-155-5p and Antagonist miR-324-5p formulated with chitosan. Total RNA was extracted from nine samples (three as control and six as treatment), and prepared for cDNA synthesis. Expression of RNA and mRNA target was measured using q-PCR Biorad CFX96 C.100 and Gen Ex 7 software. Statistics analysis was measured using SPSS 16.0. Results: The administration of combination microRNA encapsulated with chitosan affect the expression of miR-155-5p and miR-324-5p endogen (p <0.05). The expression of mRNA target HIF1α and GLI1 was down regulated after treatment. The correlation between expression of microRNA and mRNA target was strongly (p <0.05). Conclusion: This study successfully presented effects of combination of mimic miR-155-5p and antagonist miR-324-5p encapsulated chitosan which be considered as a potential therapy targets for ovarium cancer.en_US
dc.format.extent462
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoen_US
dc.publisherWest Asia Organization for Cancer Prevention (WAOCP)en_US
dc.relation.ispartofAsian Pacific Journal of Cancer Preventionen_US
dc.relation.isversionofhttps://dx.doi.org/10.31557/APJCP.2020.21.9.2603
dc.subjectMimic miR-155-5pen_US
dc.subjectAntagonist miR-324-5pen_US
dc.subjectChitosanen_US
dc.subjectCell line SKOV3en_US
dc.subjectMolecular Medicineen_US
dc.titleThe Effects of Combination of Mimic miR-155-5p and Antagonist miR-324-5p Encapsulated Chitosan in Ovarian Cancer SKOV3en_US
dc.typeTexten_US
dc.typeResearch Articlesen_US
dc.contributor.departmentStudy Program of Biotechnology, Graduate School, Universitas Gadjah Mada, Yogyakarta, Indonesia.en_US
dc.contributor.departmentFaculty of Medicine, Public Health, and Nursing, Universitas Gadjah Mada, Yogyakarta, Indonesia.en_US
dc.contributor.departmentFaculty of Medicine, Public Health, and Nursing, Universitas Gadjah Mada, Yogyakarta, Indonesia.en_US
dc.contributor.departmentFaculty of Pharmacy, Universitas Gadjah Mada, Yogyakarta, Indonesia.en_US
dc.contributor.departmentUniversitas Jenderal Soedirman, Central Java, Indonesia.en_US
dc.contributor.departmentFaculty of Medicine, Public Health, and Nursing, Universitas Gadjah Mada, Yogyakarta, Indonesia.en_US
dc.contributor.departmentFaculty of Medicine, Public Health, and Nursing, Universitas Gadjah Mada, Yogyakarta, Indonesia.en_US
dc.citation.volume21
dc.citation.issue9
dc.citation.spage2603
dc.citation.epage2608


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