HSP90 inhibitor (NVP-AUY922) enhances the anti-cancer effect of BCL-2 inhibitor (ABT-737) in small cell lung cancer expressing BCL-2

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dc.contributor.authorYang, Hannahko
dc.contributor.authorLee, Mi-Heeko
dc.contributor.authorPark, Intaeko
dc.contributor.authorJeon, Hanwoolko
dc.contributor.authorChoi, Junyoungko
dc.contributor.authorSeo, Seyoungko
dc.contributor.authorKim, Sang-Weko
dc.contributor.authorKoh, Gou Youngko
dc.contributor.authorPark, Kang-Seoko
dc.contributor.authorLee, Dae Hoko
dc.date.accessioned2018-01-22T02:04:05Z-
dc.date.available2018-01-22T02:04:05Z-
dc.date.created2017-12-18-
dc.date.created2017-12-18-
dc.date.issued2017-12-
dc.identifier.citationCANCER LETTERS, v.411, pp.19 - 26-
dc.identifier.issn0304-3835-
dc.identifier.urihttp://hdl.handle.net/10203/237152-
dc.description.abstractSmall cell lung cancer (SCLC) cannot be efficiently controlled using existing chemotherapy and radiotherapy approaches, indicating the need for new therapeutic strategies. Although ABT-737, a B-cell lymphoma-2 (BCL-2) inhibitor, exerts anticancer effects against BCL-2-expressing SCLC, monotherapy with ABT-737 is associated with limited clinical activity because of the development of resistance and toxicity. Here, we examined whether combination therapy with ABT-737 and heat shock protein 90 (HSP90) inhibitor NVP-AUY922 exerted synergistic anticancer effects on SCLC. We found that the combination of ABT-737 and NVP-AUY922 synergistically induced the apoptosis of BCL-2-expressing SCLC cells. NVP-AUY922 downregulated the expression of AKT and ERK, which activate MCL-1 to induce resistance against ABT-737. The synergistic effect was also partly due to blocking NF-kappa B activation, which induces anti-apoptosis protein expressions. However, interestingly, targeting BCL-2 and MCL-1 or BCL2 and NF-kappa B did not induce the cytotoxicity. In conclusion, our study showed that combination of BCL2 inhibitor with HSP90 inhibitor increased activity in in vitro and in vivo study in only BCL-2 expressing SCLC compared to either single BCL2 inhibitor or HSP inhibitor. The enhanced activity might be led by blocking several apoptotic pathways simultaneously rather than a specific pathway. (c) 2017 Elsevier B.V. All rights reserved.-
dc.languageEnglish-
dc.publisherELSEVIER IRELAND LTD-
dc.subjectINDUCED APOPTOSIS-
dc.subjectPHOSPHORYLATION-
dc.subjectMCL-1-
dc.subjectRESISTANCE-
dc.subjectLEUKEMIA-
dc.subjectFAMILY-
dc.subjectONCOGENESIS-
dc.subjectACTIVATION-
dc.subjectTHERAPIES-
dc.subjectHALLMARKS-
dc.titleHSP90 inhibitor (NVP-AUY922) enhances the anti-cancer effect of BCL-2 inhibitor (ABT-737) in small cell lung cancer expressing BCL-2-
dc.typeArticle-
dc.identifier.wosid000416299700003-
dc.identifier.scopusid2-s2.0-85030871645-
dc.type.rimsART-
dc.citation.volume411-
dc.citation.beginningpage19-
dc.citation.endingpage26-
dc.citation.publicationnameCANCER LETTERS-
dc.identifier.doi10.1016/j.canlet.2017.09.040-
dc.contributor.localauthorKoh, Gou Young-
dc.contributor.nonIdAuthorYang, Hannah-
dc.contributor.nonIdAuthorLee, Mi-Hee-
dc.contributor.nonIdAuthorJeon, Hanwool-
dc.contributor.nonIdAuthorChoi, Junyoung-
dc.contributor.nonIdAuthorSeo, Seyoung-
dc.contributor.nonIdAuthorKim, Sang-We-
dc.contributor.nonIdAuthorPark, Kang-Seo-
dc.contributor.nonIdAuthorLee, Dae Ho-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorSmall cell lung cancer-
dc.subject.keywordAuthorBCL-2 inhibitor-
dc.subject.keywordAuthorHSP90 inhibitor-
dc.subject.keywordAuthorCombination therapy-
dc.subject.keywordPlusINDUCED APOPTOSIS-
dc.subject.keywordPlusPHOSPHORYLATION-
dc.subject.keywordPlusMCL-1-
dc.subject.keywordPlusRESISTANCE-
dc.subject.keywordPlusLEUKEMIA-
dc.subject.keywordPlusFAMILY-
dc.subject.keywordPlusONCOGENESIS-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusTHERAPIES-
dc.subject.keywordPlusHALLMARKS-
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