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분자활성촉매반응연구단
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HS-133, a novel fluorescent phosphatidylinositol 3-kinase inhibitor as a potential imaging and anticancer agent for targeted therapy

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dc.contributor.authorLee, Ju-Hee-
dc.contributor.authorJung, Kyung Hee-
dc.contributor.authorLee, Hyunseung-
dc.contributor.authorSon, Mi Kwon-
dc.contributor.authorYun, Sun-Mi-
dc.contributor.authorAhn, Sung-Hoon-
dc.contributor.authorLee, Hyeong-Ryoon-
dc.contributor.authorSoyoung Lee-
dc.contributor.authorDonghee Kim-
dc.contributor.authorSungwoo Hong-
dc.contributor.authorHong, Soon-Sun-
dc.date.available2015-04-19T10:57:17Z-
dc.date.created2015-01-27-
dc.date.issued2014-10-
dc.identifier.issn1949-2553-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/764-
dc.description.abstractAs PI3K/Akt signaling is frequently deregulated in a wide variety of human tumors, PI3K inhibitors are an emerging class of drugs for cancer treatment. The monitoring of the drug behavior and distribution in the biological system can play an important role for targeted therapy and provide information regarding the response or resistance to available therapies. In this study, therefore, we have developed a family of xanthine derivatives, serving as a dual function exhibiting fluorescence, as well as inhibiting PI3K. Among them, HS-133 showed anti-proliferative effects and was monitored for its subcellular localization by a fluorescence microscopy. HS-133 suppressed the PI3K/Akt pathway and induced cell cycle arrest at the G0/G1 phase. The induction of apoptosis by HS-133 was confirmed by the increases of the cleaved PARP, caspase-3, and caspase-8. Furthermore, HS-133 decreased the protein expression of HIF-1α and VEGF, as well inhibited the tube formation and migration of the human umbilical vein endothelial cells. In vivo imaging also showed that tumors were visualized fluorescent with HS-133, and its oral administration significantly inhibited the growth of tumor in SkBr3 mouse xenograft models. Thus, we suggest that HS-133 may be used as a fluorescent anticancer agent against human breast cancer.-
dc.description.uri1-
dc.language영어-
dc.publisherIMPACT JOURNALS LLC-
dc.subjectAnticancer, Targeted therapy, PI3K, Fluorescence, Imaging, Apoptosis-
dc.titleHS-133, a novel fluorescent phosphatidylinositol 3-kinase inhibitor as a potential imaging and anticancer agent for targeted therapy-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid000348036500051-
dc.identifier.scopusid2-s2.0-84930446331-
dc.identifier.rimsid17128ko
dc.contributor.affiliatedAuthorSoyoung Lee-
dc.contributor.affiliatedAuthorDonghee Kim-
dc.contributor.affiliatedAuthorSungwoo Hong-
dc.identifier.doi10.18632/oncotarget.2507-
dc.identifier.bibliographicCitationONCOTARGET, v.5, no.20, pp.10180 - 10197-
dc.citation.titleONCOTARGET-
dc.citation.volume5-
dc.citation.number20-
dc.citation.startPage10180-
dc.citation.endPage10197-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.subject.keywordPlusPHOSPHOINOSITIDE 3-KINASE-
dc.subject.keywordPlusCANCER-THERAPY-
dc.subject.keywordPlusBREAST-CANCER-
dc.subject.keywordPlusPIK3CA GENE-
dc.subject.keywordPlusPI3K-AKT PATHWAY-
dc.subject.keywordPlusHIGH-FREQUENCY-
dc.subject.keywordPlusPREVENTION-
dc.subject.keywordPlusIDENTIFICATION-
dc.subject.keywordPlusCARCINOMA-
dc.subject.keywordPlusANTITUMOR-
dc.subject.keywordAuthorAnticancer-
dc.subject.keywordAuthorTargeted therapy-
dc.subject.keywordAuthorPI3K-
dc.subject.keywordAuthorFluorescence-
dc.subject.keywordAuthorImaging-
dc.subject.keywordAuthorApoptosis-
Appears in Collections:
Center for Catalytic Hydrocarbon Functionalizations(분자활성 촉매반응 연구단) > 1. Journal Papers (저널논문)
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