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Convallaria keiskei as a novel therapeutic alternative for salivary gland cancer treatment by targeting myeloid cell leukemia-1

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dc.contributor.authorLee, Haeng-Eun-
dc.contributor.authorNam, Jeong-Seok-
dc.contributor.authorShin, Ji-Ae-
dc.contributor.authorHong, In-Sun-
dc.contributor.authorYang, In-Hyoung-
dc.contributor.authorYou, Myung-Jo-
dc.contributor.authorCho, Sung-Dae-
dc.date.accessioned2024-08-08T01:37:00Z-
dc.date.available2024-08-08T01:37:00Z-
dc.date.created2024-08-07-
dc.date.created2024-08-07-
dc.date.issued2016-04-
dc.identifier.citationHead and Neck, Vol.38, pp.E761-E770-
dc.identifier.issn1043-3074-
dc.identifier.urihttps://hdl.handle.net/10371/206956-
dc.description.abstractBackground. Various chemotherapeutic agents have been used largely for the treatment of salivary gland cancer. However, results are disappointing, and these agents can cause some serious side effects. Therefore, recent studies have focused on the possible roles of natural products to overcome these limitations. Methods. Salivary gland cancer cells treated with or without Convallaria keiskei (MECK) for 24 hours. Apoptotic changes were evaluated by live/dead assay, immunoblotting, and expression levels of caspase-3 and B-cell lymphoma-2 family member. Results. MECK significantly inhibited salivary gland cancer growth. At the molecular level, MECK dramatically reduced myeloid cell leukemia-1 (Mcl-1) in a translation-dependent manner and thereby induced apoptosis through Bax/Bid. Furthermore, we found that Mcl-1 could be a potential therapeutic target of MECK-induced apoptosis and its stability is regulated by extracellular signal-regulated kinases 1/2 (ERK1/2) signaling Conclusion. MECK can be used as a safe and efficient therapeutic alternative for the treatment of salivary gland cancer. (C) 2015 Wiley Periodicals, Inc.-
dc.language영어-
dc.publisherJohn Wiley & Sons Inc.-
dc.titleConvallaria keiskei as a novel therapeutic alternative for salivary gland cancer treatment by targeting myeloid cell leukemia-1-
dc.typeArticle-
dc.identifier.doi10.1002/hed.24096-
dc.citation.journaltitleHead and Neck-
dc.identifier.wosid000375116400091-
dc.identifier.scopusid2-s2.0-84937061162-
dc.citation.endpageE770-
dc.citation.startpageE761-
dc.citation.volume38-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorCho, Sung-Dae-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusMYC-DEPENDENT APOPTOSIS-
dc.subject.keywordPlusBCL-X-L-
dc.subject.keywordPlusTRANSLATIONAL CONTROL-
dc.subject.keywordPlusDOWN-REGULATION-
dc.subject.keywordPlusCERVICAL-CARCINOMA-
dc.subject.keywordPlusCARDIAC-GLYCOSIDES-
dc.subject.keywordPlusMEDIATED APOPTOSIS-
dc.subject.keywordPlusANTAGONIZES MCL-1-
dc.subject.keywordPlusANTICANCER AGENT-
dc.subject.keywordPlusIN-VITRO-
dc.subject.keywordAuthorsalivary gland cancer-
dc.subject.keywordAuthorapoptosis-
dc.subject.keywordAuthorConvallaria keiskei (MECK)-
dc.subject.keywordAuthormyeloid cell leukemia-1 (Mcl-1)-
dc.subject.keywordAuthorextracellular signal-regulated kinases 1/2 (ERK1/2)-
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  • Department of Dentistry
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