Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/13429
Title: Antiproliferative and apoptosis induction of α-mangostin in T47D breast cancer cells
Authors: Kritsanawong S.
Innajak S.
Imoto M.
Watanapokasin R.
Keywords: alpha mangostin
antineoplastic agent
caspase 3
caspase 9
cytochrome c
DNA
epidermal growth factor receptor 2
estrogen receptor alpha
mitogen activated protein kinase 1
mitogen activated protein kinase 3
mitogen activated protein kinase p38
phosphatidylinositol 3 kinase
plant extract
protein bcl 2
protein kinase B
protein mcl 1
Raf protein
stress activated protein kinase 1
unclassified drug
antineoplastic agent
epidermal growth factor receptor 2
ERBB2 protein, human
mangostin
xanthone derivative
antiproliferative activity
apoptosis
Article
breast cancer cell line
cell cycle
cell nucleus
cell proliferation
cell viability
colony formation
controlled study
DNA fragmentation
down regulation
drug isolation
drug mechanism
drug structure
enzyme release
fruit
Garcinia mangostana
human
human cell
IC50
mitochondrial membrane potential
priority journal
protein cleavage
protein expression
protein phosphorylation
signal transduction
T47D cell line
Western blotting
apoptosis
Breast Neoplasms
cell survival
drug effects
female
gene expression regulation
metabolism
phosphorylation
tumor cell line
Antineoplastic Agents
Apoptosis
Breast Neoplasms
Cell Line, Tumor
Cell Proliferation
Cell Survival
DNA Fragmentation
Female
Gene Expression Regulation, Neoplastic
Humans
MAP Kinase Signaling System
Membrane Potential, Mitochondrial
Phosphorylation
Receptor, ErbB-2
Xanthones
Issue Date: 2016
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.
URI: https://ir.swu.ac.th/jspui/handle/123456789/13429
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84962623421&doi=10.3892%2fijo.2016.3399&partnerID=40&md5=078d7c13cd4eba425924c821b30a40e7
ISSN: 10196439
Appears in Collections:Scopus 1983-2021

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