Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/14670
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dc.contributor.authorWatanapokasin R.
dc.contributor.authorJarinthanan F.
dc.contributor.authorJerusalmi A.
dc.contributor.authorSuksamrarn S.
dc.contributor.authorNakamura Y.
dc.contributor.authorSukseree S.
dc.contributor.authorUthaisang-Tanethpongtamb W.
dc.contributor.authorRatananukul P.
dc.contributor.authorSano T.
dc.date.accessioned2021-04-05T03:36:22Z-
dc.date.available2021-04-05T03:36:22Z-
dc.date.issued2010
dc.identifier.issn2732289
dc.identifier.other2-s2.0-77955920713
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/14670-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-77955920713&doi=10.1007%2fs12010-009-8903-6&partnerID=40&md5=0910ecf01c2abf5a04a3f50a0532414a
dc.description.abstractThe pericarp of mangosteen (Garcinia mangostana L.) is rich in various xanthones that are known to possess unique biological activities. In this work, we characterized the anti-proliferative and cytotoxic activities of mangosteen xanthones both in vitro and in mice. In vitro analysis with a human colorectal adenocarcinoma cell line, COLO 205, showed that mangosteen xanthones not only inhibit the proliferation of target cells but also induce their death by apoptosis that involves the activation of the caspase cascade. In vivo analysis using a mouse subcutaneous tumor model with COLO 205 cells showed that, at relatively low doses, the growth of tumors was repressed upon intratumoral administration of mangosteen xanthones. When a higher dose of mangosteen xanthones was administered, the size of tumors was reduced gradually, and, in some mice, the disappearance of tumors was seen. Histopathological evaluation and biochemical analysis of tumors that received mangosteen xanthones indicate the induction of apoptosis in tumors, which resulted in the repression of their growth and the reduction of their sizes. These results demonstrate the potential of mangosteen xanthones to serve as anti-cancer agents for the chemotherapy of cancer. © 2010 Springer Science+Business Media, LLC.
dc.subjectApoptosis
dc.subjectCancer Chemotherapy
dc.subjectCaspases
dc.subjectGarcinia mangostana L (mangosteen)
dc.subjectMangostin
dc.subjectActivation analysis
dc.subjectCell culture
dc.subjectCell death
dc.subjectChemotherapy
dc.subjectTumors
dc.subjectantineoplastic agent
dc.subjectcaspase
dc.subjectcaspase 3
dc.subjectcaspase 8
dc.subjectcytochrome c
dc.subjectmangosteen xanthone
dc.subjectunclassified drug
dc.subjectxanthone derivative
dc.subjectadenocarcinoma
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectanimal tissue
dc.subjectantineoplastic activity
dc.subjectapoptosis
dc.subjectarticle
dc.subjectcell proliferation
dc.subjectcell structure
dc.subjectcell viability
dc.subjectcolon adenocarcinoma
dc.subjectcolorectal cancer
dc.subjectcontrolled study
dc.subjectDNA fragmentation
dc.subjectdrug cytotoxicity
dc.subjectenzyme activation
dc.subjectenzyme activity
dc.subjectenzyme release
dc.subjectfruit
dc.subjectgrowth inhibition
dc.subjecthigh performance liquid chromatography
dc.subjecthistopathology
dc.subjecthuman
dc.subjecthuman cell
dc.subjectin vitro study
dc.subjectin vivo study
dc.subjectmale
dc.subjectmangosteen
dc.subjectmouse
dc.subjectnonhuman
dc.subjectsignal transduction
dc.subjecttumor cell
dc.subjecttumor growth
dc.subjecttumor volume
dc.subjectAnimals
dc.subjectAntineoplastic Agents, Phytogenic
dc.subjectApoptosis
dc.subjectCaspases
dc.subjectCell Line, Tumor
dc.subjectCell Proliferation
dc.subjectColorectal Neoplasms
dc.subjectEnzyme Activation
dc.subjectFemale
dc.subjectFruit
dc.subjectGarcinia mangostana
dc.subjectHumans
dc.subjectMice
dc.subjectMice, Nude
dc.subjectNeoplasms
dc.subjectPlant Extracts
dc.subjectXanthones
dc.subjectGarcinia mangostana
dc.subjectMus
dc.titlePotential of xanthones from tropical fruit mangosteen as anti-cancer agents: Caspase-dependent apoptosis induction in vitro and in mice
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationApplied Biochemistry and Biotechnology. Vol 162, No.4 (2010), p.1080-1094
dc.identifier.doi10.1007/s12010-009-8903-6
Appears in Collections:Scopus 1983-2021

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