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Antiproliferative and apoptosis induction of α-mangostin in T47D breast cancer cells

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dc.contributor.author Kritsanawong S.
dc.contributor.author Innajak S.
dc.contributor.author Imoto M.
dc.contributor.author Watanapokasin R.
dc.date.accessioned 2021-04-05T03:23:54Z
dc.date.available 2021-04-05T03:23:54Z
dc.date.issued 2016
dc.identifier.issn 10196439
dc.identifier.other 2-s2.0-84962623421
dc.identifier.uri https://ir.swu.ac.th/jspui/handle/123456789/13429
dc.identifier.uri https://www.scopus.com/inward/record.uri?eid=2-s2.0-84962623421&doi=10.3892%2fijo.2016.3399&partnerID=40&md5=078d7c13cd4eba425924c821b30a40e7
dc.description.abstract α-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.subject alpha mangostin
dc.subject antineoplastic agent
dc.subject caspase 3
dc.subject caspase 9
dc.subject cytochrome c
dc.subject DNA
dc.subject epidermal growth factor receptor 2
dc.subject estrogen receptor alpha
dc.subject mitogen activated protein kinase 1
dc.subject mitogen activated protein kinase 3
dc.subject mitogen activated protein kinase p38
dc.subject phosphatidylinositol 3 kinase
dc.subject plant extract
dc.subject protein bcl 2
dc.subject protein kinase B
dc.subject protein mcl 1
dc.subject Raf protein
dc.subject stress activated protein kinase 1
dc.subject unclassified drug
dc.subject antineoplastic agent
dc.subject epidermal growth factor receptor 2
dc.subject ERBB2 protein, human
dc.subject mangostin
dc.subject xanthone derivative
dc.subject antiproliferative activity
dc.subject apoptosis
dc.subject Article
dc.subject breast cancer cell line
dc.subject cell cycle
dc.subject cell nucleus
dc.subject cell proliferation
dc.subject cell viability
dc.subject colony formation
dc.subject controlled study
dc.subject DNA fragmentation
dc.subject down regulation
dc.subject drug isolation
dc.subject drug mechanism
dc.subject drug structure
dc.subject enzyme release
dc.subject fruit
dc.subject Garcinia mangostana
dc.subject human
dc.subject human cell
dc.subject IC50
dc.subject mitochondrial membrane potential
dc.subject priority journal
dc.subject protein cleavage
dc.subject protein expression
dc.subject protein phosphorylation
dc.subject signal transduction
dc.subject T47D cell line
dc.subject Western blotting
dc.subject apoptosis
dc.subject Breast Neoplasms
dc.subject cell survival
dc.subject drug effects
dc.subject female
dc.subject gene expression regulation
dc.subject metabolism
dc.subject phosphorylation
dc.subject tumor cell line
dc.subject Antineoplastic Agents
dc.subject Apoptosis
dc.subject Breast Neoplasms
dc.subject Cell Line, Tumor
dc.subject Cell Proliferation
dc.subject Cell Survival
dc.subject DNA Fragmentation
dc.subject Female
dc.subject Gene Expression Regulation, Neoplastic
dc.subject Humans
dc.subject MAP Kinase Signaling System
dc.subject Membrane Potential, Mitochondrial
dc.subject Phosphorylation
dc.subject Receptor, ErbB-2
dc.subject Xanthones
dc.title Antiproliferative and apoptosis induction of α-mangostin in T47D breast cancer cells
dc.type Article
dc.rights.holder Scopus
dc.identifier.bibliograpycitation International Journal of Oncology. Vol 48, No.5 (2016), p.2155-2165
dc.identifier.doi 10.3892/ijo.2016.3399


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