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pH-Sensitive Pt Nanocluster Assembly Overcomes Cisplatin Resistance and Heterogeneous Stemness of Hepatocellular Carcinoma

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dc.contributor.authorXia, HP-
dc.contributor.authorLi, FY-
dc.contributor.authorPark, W-
dc.contributor.authorWang, SF-
dc.contributor.authorYoungjin Jang-
dc.contributor.authorDu, Y-
dc.contributor.authorSeungmin Baik-
dc.contributor.authorCho, S-
dc.contributor.authorTaegyu Kang-
dc.contributor.authorKim, DH-
dc.contributor.authorLing, DS-
dc.contributor.authorHui, KM-
dc.contributor.authorTaeghwan Hyeon-
dc.date.available2018-12-13T12:22:41Z-
dc.date.created2018-03-16-
dc.date.issued2016-11-
dc.identifier.issn2374-7943-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/5014-
dc.description.abstractResponse rates to conventional chemotherapeutics remain unsatisfactory for hepatocellular carcinoma (HCC) due to the high rates of chemoresistance and recurrence. Tumor-initiating cancer stem-like cells (CSLCs) are refractory to chemotherapy, and their enrichment leads to subsequent development of chemoresistance and recurrence. To overcome the chemoresistance and stemness in HCC, we synthesized a Pt nanocluster assembly (Pt-NA) composed of assembled Pt nanoclusters incorporating a pH-sensitive polymer and HCC-targeting peptide. Pt-NA is latent in peripheral blood, readily targets disseminated HCC CSLCs, and disassembles into small Pt nanoclusters in acidic subcellular compartments, eventually inducing damage to DNA. Furthermore, treatment with Pt-NA downregulates a multitude of genes that are vital for the proliferation of HCC. Importantly, CD24+ side population (SP) CSLCs that are resistant to cisplatin are sensitive to Pt-NA, demonstrating the immense potential of Pt-NA for treating chemoresistant HCC © 2016 American Chemical Society-
dc.language영어-
dc.publisherAMER CHEMICAL SOC-
dc.titlepH-Sensitive Pt Nanocluster Assembly Overcomes Cisplatin Resistance and Heterogeneous Stemness of Hepatocellular Carcinoma-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid000390864600008-
dc.identifier.scopusid2-s2.0-85016853331-
dc.identifier.rimsid62486-
dc.contributor.affiliatedAuthorYoungjin Jang-
dc.contributor.affiliatedAuthorSeungmin Baik-
dc.contributor.affiliatedAuthorTaegyu Kang-
dc.contributor.affiliatedAuthorTaeghwan Hyeon-
dc.identifier.doi10.1021/acscentsci.6b00197-
dc.identifier.bibliographicCitationACS CENTRAL SCIENCE, v.2, no.11, pp.802 - 811-
dc.relation.isPartOfACS CENTRAL SCIENCE-
dc.citation.titleACS CENTRAL SCIENCE-
dc.citation.volume2-
dc.citation.number11-
dc.citation.startPage802-
dc.citation.endPage811-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscopus-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusPLATINUM NANOPARTICLES-
dc.subject.keywordPlusCANCER-CELLS-
dc.subject.keywordPlusTHERAPEUTIC-EFFICACY-
dc.subject.keywordPlusSILVER NANOPARTICLES-
dc.subject.keywordPlusDRUG-DELIVERY-
dc.subject.keywordPlusQUANTUM DOTS-
dc.subject.keywordPlusSELF-RENEWAL-
dc.subject.keywordPlusDNA-DAMAGE-
dc.subject.keywordPlusPHARMACOKINETICS-
dc.subject.keywordPlusBIODISTRIBUTION-
Appears in Collections:
Center for Nanoparticle Research(나노입자 연구단) > 1. Journal Papers (저널논문)
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