Please use this identifier to cite or link to this item: http://repository.i3l.ac.id/jspui/handle/123456789/154
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dc.contributor.authorKaryadi, Azrina Saraswati-
dc.date.accessioned2021-10-26T05:44:40Z-
dc.date.available2021-10-26T05:44:40Z-
dc.date.issued2019-12-19-
dc.identifier.urihttp://repository.i3l.ac.id/jspui/handle/123456789/154-
dc.description.abstractNon-coding RNAs, which made up 98% of the human genome, have immense regulatory influence in cellular functionality that have not yet been fully explored. A study conducted by Prof. Vinay Tergaongkar’s laboratory identified an important lncRNA, XXX, which deregulates NFkB biology in cancer by sustaining covalent modification of p65, thereby regulating genome-wide occupancy of p65 on targets essential to inflammation, cancer progression, and CSC maintenance. HCC made up 90% of the primary liver cancer cases, and its progression and malignancy revolve around the CSC model. Being attributed to various inflammatory etiologies, dysregulation of NFkB is a major hallmark to its development. This study explores the breadth of XXX influence on NFkB signaling in HCC by analyzing its impact of NFkB’s target gene expression, resulting stemness phenotype alterations, and drug resistance.en_US
dc.language.isoenen_US
dc.publisherIndonesia International Institute for Life Sciencesen_US
dc.relation.ispartofseriesBM 19-014;T201912014-
dc.subjecthuman genomeen_US
dc.subjectNon-coding RNAen_US
dc.subjectNFkBen_US
dc.subjectgene expressionen_US
dc.titleImplication of Xxx Silencing on Epatocellular Carcinoma Drug Esponse through NFkB Signaling Pathwayen_US
dc.typeThesisen_US
Appears in Collections:Biomedicine

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