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Myeloid cell leukemia-1 expression in cancers of the oral cavity: a scoping review

DC Field Value Language
dc.contributor.authorChoi, Su-Jung-
dc.contributor.authorSwarup, Neeti-
dc.contributor.authorShin, Ji-Ae-
dc.contributor.authorHong, Seong-Doo-
dc.contributor.authorCho, Sung-Dae-
dc.date.accessioned2022-06-21T08:01:13Z-
dc.date.available2022-06-21T08:01:13Z-
dc.date.created2022-05-24-
dc.date.issued2022-05-
dc.identifier.citationCancer Cell International, Vol.22 No.1, p. 182-
dc.identifier.issn1475-2867-
dc.identifier.urihttps://hdl.handle.net/10371/182631-
dc.description.abstractBackground B cell lymphoma-2 (Bcl-2) family members play important roles in cell survival as well as cell death. The role of myeloid cell leukemia-1 (Mcl-1), an important member of the Bcl-2 family, is well established in hematopoietic malignancies. However, the association between Mcl-1 and oral cavity, cancers is not clearly defined. Methods A scoping review was conducted until June 30, 2021, using four major databases, PubMed, Scopus, Web of Science, and Embase. Medical subject headings keywords for Mcl-1, along with its other identifiers, and head and neck cancers (only oral cavity tumors) were used to evaluate the expression, function, molecular association, and therapeutic approach of Mcl-1 in oral cavity cancers and precancers. Findings Mcl-1 expression was associated with the progression of oral cavity cancers. The molecular mechanism and pathways of Mcl-1 in oral cavity cancers established via experimental results have been highlighted in this review. Moreover, the various synthetic and naturally derived therapeutic agents targeting Mcl-1 have been documented. Novelty/Improvement Based on our present review, Mcl-1 appears to be an effective anticancer target that can be used in the therapeutic management of oral cancers.-
dc.language영어-
dc.publisherBioMed Central-
dc.titleMyeloid cell leukemia-1 expression in cancers of the oral cavity: a scoping review-
dc.typeArticle-
dc.identifier.doi10.1186/s12935-022-02603-0-
dc.citation.journaltitleCancer Cell International-
dc.identifier.wosid000791777400003-
dc.identifier.scopusid2-s2.0-85129594918-
dc.citation.number1-
dc.citation.startpage182-
dc.citation.volume22-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorHong, Seong-Doo-
dc.contributor.affiliatedAuthorCho, Sung-Dae-
dc.type.docTypeReview-
dc.description.journalClass1-
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