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Apoptosis: a Janus bifrons in T-cell immunotherapy

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dc.contributor.authorLee, Yong Gu-
dc.contributor.authorYang, Nicholas-
dc.contributor.authorChun, Inkook-
dc.contributor.authorPorazzi, Patrizia-
dc.contributor.authorCarturan, Alberto-
dc.contributor.authorParuzzo, Luca-
dc.contributor.authorSauter, Christopher Tor-
dc.contributor.authorGuruprasad, Puneeth-
dc.contributor.authorPajarillo, Raymone-
dc.contributor.authorRuella, Marco-
dc.date.accessioned2023-07-27T12:11:29Z-
dc.date.available2023-07-27T12:11:29Z-
dc.date.created2023-06-05-
dc.date.issued2023-04-
dc.identifier.issn2051-1426-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/188334-
dc.description.abstractImmunotherapy has revolutionized the treatment of cancer. In particular, immune checkpoint blockade, bispecific antibodies, and adoptive T-cell transfer have yielded unprecedented clinical results in hematological malignancies and solid cancers. While T cell-based immunotherapies have multiple mechanisms of action, their ultimate goal is achieving apoptosis of cancer cells. Unsurprisingly, apoptosis evasion is a key feature of cancer biology. Therefore, enhancing cancer cells' sensitivity to apoptosis represents a key strategy to improve clinical outcomes in cancer immunotherapy. Indeed, cancer cells are characterized by several intrinsic mechanisms to resist apoptosis, in addition to features to promote apoptosis in T cells and evade therapy. However, apoptosis is double-faced: when it occurs in T cells, it represents a critical mechanism of failure for immunotherapies. This review will summarize the recent efforts to enhance T cell-based immunotherapies by increasing apoptosis susceptibility in cancer cells and discuss the role of apoptosis in modulating the survival of cytotoxic T lymphocytes in the tumor microenvironment and potential strategies to overcome this issue.-
dc.language영어-
dc.language.isoen-
dc.publisherBioMed Central-
dc.titleApoptosis: a Janus bifrons in T-cell immunotherapy-
dc.typeArticle-
dc.contributor.affiliatedAuthorLee, Yong Gu-
dc.identifier.doi10.1136/jitc-2022-005967-
dc.identifier.scopusid2-s2.0-85152464607-
dc.identifier.wosid000989727900004-
dc.identifier.bibliographicCitationJournal for ImmunoTherapy of Cancer, v.11, no.4, pp.1 - 13-
dc.relation.isPartOfJournal for ImmunoTherapy of Cancer-
dc.citation.titleJournal for ImmunoTherapy of Cancer-
dc.citation.volume11-
dc.citation.number4-
dc.citation.startPage1-
dc.citation.endPage13-
dc.type.rimsART-
dc.type.docTypeReview-
dc.description.journalClass1-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaOncology-
dc.relation.journalResearchAreaImmunology-
dc.relation.journalWebOfScienceCategoryOncology-
dc.relation.journalWebOfScienceCategoryImmunology-
dc.subject.keywordPlusTRAIL-INDUCED APOPTOSIS-
dc.subject.keywordPlusHUMAN TUMOR-CELLS-
dc.subject.keywordPlusLYMPHOCYTE APOPTOSIS-
dc.subject.keywordPlusINDUCE APOPTOSIS-
dc.subject.keywordPlusDOWN-REGULATION-
dc.subject.keywordPlusBREAST-CANCER-
dc.subject.keywordPlusLIGAND TRAIL-
dc.subject.keywordPlusBCL-2-
dc.subject.keywordPlusDEATH-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordAuthorimmunotherapy-
dc.subject.keywordAuthoradoptive-
dc.subject.keywordAuthorcytotoxicity-
dc.subject.keywordAuthorimmunologic-
dc.identifier.urlhttps://www.proquest.com/docview/2800251219?accountid=11283-
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