Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/13429
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dc.contributor.authorKritsanawong S.
dc.contributor.authorInnajak S.
dc.contributor.authorImoto M.
dc.contributor.authorWatanapokasin R.
dc.date.accessioned2021-04-05T03:23:54Z-
dc.date.available2021-04-05T03:23:54Z-
dc.date.issued2016
dc.identifier.issn10196439
dc.identifier.other2-s2.0-84962623421
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/13429-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84962623421&doi=10.3892%2fijo.2016.3399&partnerID=40&md5=078d7c13cd4eba425924c821b30a40e7
dc.description.abstractα-Mangostin extracted from mangosteen, Garcinia mangostana Linn. is known as 'queen of fruits'. The anticancer activity of α-mangostin through apoptosis induction and related signaling pathways in human breast cancer T47D cells was investigated. Human epidermal growth factor receptor 2 (HER2) and mitogen-activated protein kinase (MAPK) signaling have been shown to play important roles in apoptosis. The results showed that α-mangostin induced cell proliferation inhibition, DNA fragmentation, nuclear condensation, increased cleaved caspase-3 and cleaved caspase-9, but decreased Bcl-2 and Mcl-1 expression. Mitochondrial dysfunction and cytochrome c release were also detected. In addition, phosphorylation of ERα, HER2, PI3K, Akt and ERK1/2 were downregulated whereas p-JNK1/2 and p-p38 were upregulated. These results indicated that α-mangostin induced apoptosis associated with HER2/PI3K/Akt and MAPK signaling pathways suggesting that α-mangostin may be used as food supplement or a potential therapeutic compound for breast cancer.
dc.subjectalpha mangostin
dc.subjectantineoplastic agent
dc.subjectcaspase 3
dc.subjectcaspase 9
dc.subjectcytochrome c
dc.subjectDNA
dc.subjectepidermal growth factor receptor 2
dc.subjectestrogen receptor alpha
dc.subjectmitogen activated protein kinase 1
dc.subjectmitogen activated protein kinase 3
dc.subjectmitogen activated protein kinase p38
dc.subjectphosphatidylinositol 3 kinase
dc.subjectplant extract
dc.subjectprotein bcl 2
dc.subjectprotein kinase B
dc.subjectprotein mcl 1
dc.subjectRaf protein
dc.subjectstress activated protein kinase 1
dc.subjectunclassified drug
dc.subjectantineoplastic agent
dc.subjectepidermal growth factor receptor 2
dc.subjectERBB2 protein, human
dc.subjectmangostin
dc.subjectxanthone derivative
dc.subjectantiproliferative activity
dc.subjectapoptosis
dc.subjectArticle
dc.subjectbreast cancer cell line
dc.subjectcell cycle
dc.subjectcell nucleus
dc.subjectcell proliferation
dc.subjectcell viability
dc.subjectcolony formation
dc.subjectcontrolled study
dc.subjectDNA fragmentation
dc.subjectdown regulation
dc.subjectdrug isolation
dc.subjectdrug mechanism
dc.subjectdrug structure
dc.subjectenzyme release
dc.subjectfruit
dc.subjectGarcinia mangostana
dc.subjecthuman
dc.subjecthuman cell
dc.subjectIC50
dc.subjectmitochondrial membrane potential
dc.subjectpriority journal
dc.subjectprotein cleavage
dc.subjectprotein expression
dc.subjectprotein phosphorylation
dc.subjectsignal transduction
dc.subjectT47D cell line
dc.subjectWestern blotting
dc.subjectapoptosis
dc.subjectBreast Neoplasms
dc.subjectcell survival
dc.subjectdrug effects
dc.subjectfemale
dc.subjectgene expression regulation
dc.subjectmetabolism
dc.subjectphosphorylation
dc.subjecttumor cell line
dc.subjectAntineoplastic Agents
dc.subjectApoptosis
dc.subjectBreast Neoplasms
dc.subjectCell Line, Tumor
dc.subjectCell Proliferation
dc.subjectCell Survival
dc.subjectDNA Fragmentation
dc.subjectFemale
dc.subjectGene Expression Regulation, Neoplastic
dc.subjectHumans
dc.subjectMAP Kinase Signaling System
dc.subjectMembrane Potential, Mitochondrial
dc.subjectPhosphorylation
dc.subjectReceptor, ErbB-2
dc.subjectXanthones
dc.titleAntiproliferative and apoptosis induction of α-mangostin in T47D breast cancer cells
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationInternational Journal of Oncology. Vol 48, No.5 (2016), p.2155-2165
dc.identifier.doi10.3892/ijo.2016.3399
Appears in Collections:Scopus 1983-2021

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