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Immune-mediated tumor evolution: Nanog links the emergence of a stem like cancer cell state and immune evasion

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dc.contributor.authorMao, Chih-Ping-
dc.contributor.authorWu, T. C.-
dc.contributor.authorSong, Kwon-Ho-
dc.contributor.authorKim, Tae Woo-
dc.date.accessioned2021-09-05T07:30:28Z-
dc.date.available2021-09-05T07:30:28Z-
dc.date.created2021-06-15-
dc.date.issued2014-07-
dc.identifier.issn2162-4011-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/98145-
dc.description.abstractTumor cells undergo molecular evolution under immune pressure. Using a murine metastatic lung cancer model, we recently reported that evolutionary pressure enforced through vaccination incites gain of Nanog, a master transcription factor that mediates both emergence of a stem-like cancer cell state and immune evasion. Thus, therapeutic strategies aiming to blunt NANOG's expression in patient tumors may improve the clinical management of cancer.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherTAYLOR & FRANCIS INC-
dc.subjectSURVIVAL-
dc.subjectAKT-
dc.subjectEXPRESSION-
dc.titleImmune-mediated tumor evolution: Nanog links the emergence of a stem like cancer cell state and immune evasion-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Tae Woo-
dc.identifier.doi10.4161/21624011.2014.947871-
dc.identifier.scopusid2-s2.0-84911372296-
dc.identifier.wosid000346921100014-
dc.identifier.bibliographicCitationONCOIMMUNOLOGY, v.3, no.7-
dc.relation.isPartOfONCOIMMUNOLOGY-
dc.citation.titleONCOIMMUNOLOGY-
dc.citation.volume3-
dc.citation.number7-
dc.type.rimsART-
dc.type.docTypeEditorial Material-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaOncology-
dc.relation.journalResearchAreaImmunology-
dc.relation.journalWebOfScienceCategoryOncology-
dc.relation.journalWebOfScienceCategoryImmunology-
dc.subject.keywordPlusSURVIVAL-
dc.subject.keywordPlusAKT-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordAuthorcytotoxic T lymphocytes-
dc.subject.keywordAuthorimmune-resistant-
dc.subject.keywordAuthorimmune surveillance-
dc.subject.keywordAuthorNanog-
dc.subject.keywordAuthorstem-like phenotype-
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