Please use this identifier to cite or link to this item: http://hdl.handle.net/11455/70586
DC FieldValueLanguage
dc.contributor.authorTsou, M.F.en_US
dc.contributor.authorPeng, C.T.en_US
dc.contributor.authorShih, M.C.en_US
dc.contributor.authorYang, J.S.en_US
dc.contributor.authorLu, C.C.en_US
dc.contributor.authorChiang, J.H.en_US
dc.contributor.authorWu, C.L.en_US
dc.contributor.authorLin, J.P.en_US
dc.contributor.authorLo, C.en_US
dc.contributor.authorFan, M.J.en_US
dc.contributor.authorChung, J.G.en_US
dc.date2009zh_TW
dc.date.accessioned2014-06-11T06:00:03Z-
dc.date.available2014-06-11T06:00:03Z-
dc.identifier.issn0145-2126zh_TW
dc.identifier.urihttp://hdl.handle.net/11455/70586-
dc.description.abstractMany evidences have shown that dietary intake of cruciferous vegetables could protect against the risk of various types of malignancies. Benzyl isothiocyanate (BITC), one of the compounds from cruciferous vegetables, had shown induced cell cycle arrest and apoptosis in cancer cells. However, there is no available information to address that BITC affects murine leukemia cells in vitro and in vivo. Here, we investigated in vitro effects of BITC on murine leukemia WEHI-3 cells. BITC decreased the percentage of viable cells via GO/G1 arrest and apoptosis in WEHI-3 cells. BITC induced apoptosis through the dysfunction of mitochondria (decreased the levels of mitochondria membrane potential) and activation of caspase-3. Then we investigated in vivo effects of BITC on murine leukemia WEHI-3 cells and the results indicated that BITC decreased the weights of liver and spleen and it also decreased the percentage of CD11b and Mac-3 markers, indicating that the differentiation of the precursor of macrophage and B cells was inhibited. BITC promoted the activity of macrophage phagocytosis in cells which are isolated from PBMC and peritoneal (i.p.). Taken together, BITC can affect WEHI-3 cells in vitro and in vivo. Crown Copyright (C) 2009 Published by Elsevier Ltd. All rights reserved.en_US
dc.language.isoen_USzh_TW
dc.relationLeukemia Researchen_US
dc.relation.ispartofseriesLeukemia Research, Volume 33, Issue 11, Page(s) 1505-1511.en_US
dc.relation.urihttp://dx.doi.org/10.1016/j.ieukres.2009.01.030en_US
dc.subjectBenzyl isothiocyanate (BITC)en_US
dc.subjectWEHI-3 leukemia cellsen_US
dc.subjectBALB/c miceen_US
dc.subjectImmuneen_US
dc.subjectresponseen_US
dc.subjectCytotoxicityen_US
dc.subjectmitochondrial death pathwayen_US
dc.subjectactivated protein-kinasesen_US
dc.subjectcycle arresten_US
dc.subjectcancer-risken_US
dc.subjectcarcinoma-cellsen_US
dc.subjectcrude extractsen_US
dc.subjectbreast-canceren_US
dc.subjecta/j miceen_US
dc.subjectkappa-ben_US
dc.subjectapoptosisen_US
dc.titleBenzyl isothiocyanate inhibits murine WEHI-3 leukemia cells in vitro and promotes phagocytosis in BALB/c mice in vivoen_US
dc.typeJournal Articlezh_TW
dc.identifier.doi10.1016/j.ieukres.2009.01.030zh_TW
item.openairetypeJournal Article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextno fulltext-
item.grantfulltextnone-
item.languageiso639-1en_US-
item.cerifentitytypePublications-
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