Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/101389
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dc.contributorDepartment of Biomedical Engineeringen_US
dc.creatorWu, Jen_US
dc.creatorTan, Zen_US
dc.creatorChen, Jen_US
dc.creatorDong, Cen_US
dc.date.accessioned2023-09-13T09:31:26Z-
dc.date.available2023-09-13T09:31:26Z-
dc.identifier.issn1420-3049en_US
dc.identifier.urihttp://hdl.handle.net/10397/101389-
dc.language.isoenen_US
dc.publisherMolecular Diversity Preservation International (MDPI)en_US
dc.rights© 2015 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons by Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).en_US
dc.rightsThe following publication Wu, J., Tan, Z., Chen, J., & Dong, C. (2015). Cyclovirobuxine D inhibits cell proliferation and induces mitochondria-mediated apoptosis in human gastric cancer cells. Molecules, 20(11), 20659-20668 is available at https://doi.org/10.3390/molecules201119729.en_US
dc.subjectApoptosisen_US
dc.subjectCell cycleen_US
dc.subjectCyclovirobuxine Den_US
dc.subjectGastric canceren_US
dc.subjectMitochondriaen_US
dc.titleCyclovirobuxine D inhibits cell proliferation and induces mitochondria-mediated apoptosis in human gastric cancer cellsen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage20659en_US
dc.identifier.epage20668en_US
dc.identifier.volume20en_US
dc.identifier.issue11en_US
dc.identifier.doi10.3390/molecules201119729en_US
dcterms.abstractGastric cancer is one of the most common malignant cancers, with high death rates, poor prognosis and limited treatment methods. Cyclovirobuxine D (CVB-D) is the main active component of the traditional Chinese medicine Buxus microphylla. In the present study, we test the effects of CVB-D on gastric cancer cells and the underlying mechanisms of action. CVB-D reduced cell viability and colony formation ability of MGC-803 and MKN28 cells in a time- and concentration-dependent manner. Flow cytometry showed that cell cycle of CVB-D treated cells was arrested at the S-phase. CVB-D also induced apoptosis in MGC-803 and MKN28 cells, especially early stage apoptosis. Furthermore, mitochondria membrane potential (Δψm) was reduced and apoptosis-related proteins, cleaved Caspase-3 and Bax/Bcl-2, were up-regulated in CVB-D-treated MGC-803 and MKN28 cells. Taken together, our studies found that CVB-D plays important roles in inhibition of gastric tumorigenesis via arresting cell cycle and inducing mitochondria-mediated apoptosis, suggesting the potential application of CVB-D in gastric cancer therapy.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationMolecules, Nov. 2015, v. 20, no. 11, p. 20659-20668en_US
dcterms.isPartOfMoleculesen_US
dcterms.issued2015-11-
dc.identifier.scopus2-s2.0-84949945362-
dc.identifier.pmid26610442-
dc.description.validate202309 bckwen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_Others [non PolyU]-
dc.description.fundingSourceOthersen_US
dc.description.fundingTextNational Natural Science Foundation of China; Chenxing Young Scholars Program B of Shanghai Jiao Tong University; New Teachers Start Program of Shanghai Jiao Tong Universityen_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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