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A novel antitumor piperazine alkyl compound causes apoptosis by inducing RhoB expression via ROS-mediated c-Abl/p38 MAPK signaling

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dc.contributor.authorChung, Kyung-Sook-
dc.contributor.authorHan, Gyoonhee-
dc.contributor.authorKim, Bo-Kyung-
dc.contributor.authorKim, Hwan-Mook-
dc.contributor.authorYang, Jee Sun-
dc.contributor.authorAhn, Jiwon-
dc.contributor.authorLee, Kyeong-
dc.contributor.authorSong, Kyung-Bin-
dc.contributor.authorWon, Misun-
dc.date.accessioned2024-08-08T01:31:37Z-
dc.date.available2024-08-08T01:31:37Z-
dc.date.issued2013-12-
dc.identifier.issn0344-5704-
dc.identifier.issn1432-0843-
dc.identifier.urihttps://scholarworks.dongguk.edu/handle/sw.dongguk/15432-
dc.description.abstractWe investigated the action mechanism of a novel anticancer compound, KR28 (1-allyl-4-dodecanoyl-1-ethyl-piperazin-1-ium; bromide), to induce apoptosis of human prostate carcinoma PC-3 cells. To explore an apoptotic signaling of KR28, we used ROS assay, SRB assay, flow cytometry analysis, reporter assay, xenograft assay, Western blotting, and RT-PCR analysis. The growth inhibitory action of KR28 is cell line specific, impeding the growth of prostate carcinoma PC-3 and stomach carcinoma NUGC-3 cells. KR28 showed strong antitumor activity in PC-3 mouse xenograft model. KR28 increased ROS production, leading to nuclear c-Abl expression, which in turn activated p38 mitogen-activated protein kinase (MAPK) to enhance the expression of RhoB, an apoptosis inducer. The KR28-induced apoptosis was abrogated by the ROS scavenger N-acetylcysteine and by knockdown of c-Abl, p38 MAPK, or ATF2. Moreover, the p300 binding site and two CCAAT boxes in the RhoB promoter appear to be involved in ROS-mediated RhoB expression in the presence of KR28. The antitumor agent KR28 induces apoptosis of PC-3 cells by ROS-mediated RhoB expression via c-Abl upregulation and activation of p38 MAPK/ATF-2.-
dc.format.extent10-
dc.language영어-
dc.language.isoENG-
dc.publisherSPRINGER-
dc.titleA novel antitumor piperazine alkyl compound causes apoptosis by inducing RhoB expression via ROS-mediated c-Abl/p38 MAPK signaling-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1007/s00280-013-2310-y-
dc.identifier.scopusid2-s2.0-84890352287-
dc.identifier.wosid000327387000017-
dc.identifier.bibliographicCitationCANCER CHEMOTHERAPY AND PHARMACOLOGY, v.72, no.6, pp 1315 - 1324-
dc.citation.titleCANCER CHEMOTHERAPY AND PHARMACOLOGY-
dc.citation.volume72-
dc.citation.number6-
dc.citation.startPage1315-
dc.citation.endPage1324-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaOncology-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryOncology-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.subject.keywordPlusABL TYROSINE KINASE-
dc.subject.keywordPlusN-TERMINAL KINASE-
dc.subject.keywordPlusDNA-DAMAGE-
dc.subject.keywordPlusCANCER-CELLS-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusSTRESS-
dc.subject.keywordPlusFARNESYLTRANSFERASE-
dc.subject.keywordPlusPROGRESSION-
dc.subject.keywordAuthorProstate cancer-
dc.subject.keywordAuthorRhoB-
dc.subject.keywordAuthorROS-
dc.subject.keywordAuthorc-Abl-
dc.subject.keywordAuthorp38 MAPK-
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