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Recent Advances in the Development of TGF-β Signaling Inhibitors for Anticancer Therapy

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dc.contributor.authorHo-Jae Lee-
dc.date.available2020-12-31T05:40:09Z-
dc.date.created2020-12-31-
dc.date.issued2020-12-
dc.identifier.issn2288-3649-
dc.identifier.urihttps://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/79552-
dc.description.abstractTGF-β is a multifunctional cytokine that plays an important role in both physiologic and pathologic processes, including cancer. Importantly, TGF-β has a dual role in tumorigenesis, acting as a tumor suppressor or a tumor promoter, depending on the stage of tumor development. The aberrantly upregulated production of TGF-β has been strongly implicated in tumor progression, angiogenesis, and metastasis, as well as immune evasion. Therefore, hyperactivated TGF-β signaling is considered a potential therapeutic target for cancer therapy. Numerous inhibitors of overactivated TGF-β signaling have been developed, and some of them are currently in clinical trials. This review focuses on the TGF-β signaling that contributes to tumor progression and immune evasion in the tumor microenvironment and presents recent achievements on TGF-β signaling inhibition as a single or combined therapeutic approach in cancer therapy. Key Words TGF-b, Tumor microenvironment, Tumor escape, Antineoplastic agents, Immune checkpoint inhibitors-
dc.language영어-
dc.language.isoen-
dc.publisher대한암예방학회-
dc.relation.isPartOf대한암예방학회지-
dc.titleRecent Advances in the Development of TGF-β Signaling Inhibitors for Anticancer Therapy-
dc.title.alternativeRecent Advances in the Development of TGF-β Signaling Inhibitors for Anticancer Therapy-
dc.typeArticle-
dc.type.rimsART-
dc.description.journalClass2-
dc.identifier.wosid000607679900003-
dc.identifier.bibliographicCitation대한암예방학회지, v.25, no.4, pp.213 - 222-
dc.identifier.kciidART002665276-
dc.description.isOpenAccessN-
dc.citation.endPage222-
dc.citation.startPage213-
dc.citation.title대한암예방학회지-
dc.citation.volume25-
dc.citation.number4-
dc.contributor.affiliatedAuthorHo-Jae Lee-
dc.subject.keywordAuthorTGF-b-
dc.subject.keywordAuthorTumor microenvironment-
dc.subject.keywordAuthorTumor escape-
dc.subject.keywordAuthorAntineoplastic agents-
dc.subject.keywordAuthorImmune checkpoint inhibitors-
dc.description.journalRegisteredClasskci-
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