File Download

  • Find it @ UNIST can give you direct access to the published full text of this article. (UNISTARs only)
Related Researcher

서판길

Suh, Pann-Ghill
Read More

Views & Downloads

Detailed Information

Cited time in webofscience Cited time in scopus
Metadata Downloads

Full metadata record

DC Field Value Language
dc.citation.number 1 -
dc.citation.startPage 431 -
dc.citation.title BMC CANCER -
dc.citation.volume 14 -
dc.contributor.author Park, Hye-Kyung -
dc.contributor.author Lee, Ji-Eun -
dc.contributor.author Lim, Jaehwa -
dc.contributor.author Jo, Da-Eun -
dc.contributor.author Park, Soo-Ah -
dc.contributor.author Suh, Pann-Ghill -
dc.contributor.author Kang, Byoung Heon -
dc.date.accessioned 2023-12-22T02:38:20Z -
dc.date.available 2023-12-22T02:38:20Z -
dc.date.created 2014-08-20 -
dc.date.issued 2014-06 -
dc.description.abstract Background: A common approach to cancer therapy in clinical practice is the combination of several drugs to boost the anticancer activity of available drugs while suppressing their unwanted side effects. In this regard, we examined the efficacy of combination treatment with the widely-used genotoxic drug doxorubicin and the mitochondriotoxic Hsp90 inhibitor gamitrinib to exploit disparate stress signaling pathways for cancer therapy.Methods: The cytotoxicity of the drugs as single agents or in combination against several cancer cell types was analyzed by MTT assay and the synergism of the drug combination was evaluated by calculating the combination index. To understand the molecular mechanism of the drug synergism, stress signaling pathways were analyzed after drug combination. Two xenograft models with breast and prostate cancer cells were used to evaluate anticancer activity of the drug combination in vivo. Cardiotoxicity was assessed by tissue histology and serum creatine phosphokinase concentration.Results: Gamitrinib sensitized various human cancer cells to doxorubicin treatment, and combination treatment with the two drugs synergistically increased apoptosis. The cytotoxicity of the drug combination involved activation and mitochondrial accumulation of the proapoptotic Bcl-2 family member Bim. Activation of Bim was associated with increased expression of the proapoptotic transcription factor C/EBP-homologous protein and enhanced activation of the stress kinase c-Jun N-terminal kinase. Combined drug treatment with doxorubicin and gamitrinib dramatically reduced in vivo tumor growth in prostate and breast xenograft models without increasing cardiotoxicity.Conclusions: The drug combination showed synergistic anticancer activities toward various cancer cells without aggravating the cardiotoxic side effects of doxorubicin, suggesting that the full therapeutic potential of doxorubicin can be unleashed through combination with gamitrinib. -
dc.identifier.bibliographicCitation BMC CANCER, v.14, no.1, pp.431 -
dc.identifier.doi 10.1186/1471-2407-14-431 -
dc.identifier.issn 1471-2407 -
dc.identifier.scopusid 2-s2.0-84902051863 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/5494 -
dc.identifier.url http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84902051863 -
dc.identifier.wosid 000338962300001 -
dc.language 영어 -
dc.publisher BIOMED CENTRAL LTD -
dc.title Combination treatment with doxorubicin and gamitrinib synergistically augments anticancer activity through enhanced activation of Bim -
dc.type Article -
dc.description.isOpenAccess TRUE -
dc.relation.journalWebOfScienceCategory Oncology -
dc.relation.journalResearchArea Oncology -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -

qrcode

Items in Repository are protected by copyright, with all rights reserved, unless otherwise indicated.