Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/14619
Full metadata record
DC FieldValueLanguage
dc.contributor.authorPhonnok S.
dc.contributor.authorTanechpongtamb W.U.
dc.contributor.authorWongsatayanon B.T.
dc.date.accessioned2021-04-05T03:36:00Z-
dc.date.available2021-04-05T03:36:00Z-
dc.date.issued2010
dc.identifier.issn7173458
dc.identifier.other2-s2.0-79960762004
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/14619-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-79960762004&doi=10.2225%2fvol13-issue5-fulltext-7&partnerID=40&md5=389d8d98120c55724b28631a2074341a
dc.description.abstractThe problems of systemic toxicity and drug resistance in cancer chemotherapy urge the continuing discovery of new anticancer agents. We explored the specific anticancer activity from microbial metabolites to find new lead compound. 394 microbial extracts were evaluated on anti-proliferative activity against 4 cancer cell lines using MTT assay. Of these, 20 samples showed varying degree of cytotoxicity but specifically to the cancer cell lines since the growth of normal cells was not significantly inhibited by 1 mg/ml of each cell extracts. The 4 most potent extracts exhibited strongest growth inhibition to each cancer cell type were selected for further studied. Cell morphological changes such as cell shrinkage, lose of surface contact and blebbing were observed in all treated cancer cells. DNA-binding dye staining demonstrated nuclear condensation and fragmentation. Chromosomal DNA cleavage detected as DNA ladder pattern by gel electrophoresis including activation of cellular caspase-3 activity, a hallmark of apoptosis, were observed in all treated cancer cell lines. These characteristics suggested the mechanism of apoptosis cell death induced by the extracts. No growth inhibition and apoptosis characteristic were detected in normal cells even at high concentration used suggesting the selective cytotoxicity and potential candidates to develop as anticancer agents. © 2010 by Pontificia Universidad Católica de Valparaíso, Chile.
dc.subjectAnti-cancer agents
dc.subjectAnti-proliferative
dc.subjectAnticancer
dc.subjectAnticancer activities
dc.subjectApoptosis-inducing activity
dc.subjectBioactive compounds
dc.subjectCancer cell lines
dc.subjectCancer cells
dc.subjectCancer Chemotherapy
dc.subjectCaspase-3
dc.subjectCaspases
dc.subjectCell extracts
dc.subjectCell-shrinkage
dc.subjectDNA cleavage
dc.subjectDNA ladder
dc.subjectDNA-binding
dc.subjectDrug resistance
dc.subjectGel electrophoresis
dc.subjectGrowth inhibition
dc.subjectHigh concentration
dc.subjectMicrobial products
dc.subjectMorphological changes
dc.subjectMTT assays
dc.subjectSurface contact
dc.subjectCell culture
dc.subjectChemotherapy
dc.subjectDiseases
dc.subjectDNA
dc.subjectElectrophoresis
dc.subjectLead compounds
dc.subjectMetabolism
dc.subjectMetabolites
dc.subjectCell death
dc.subjectcaspase 3
dc.subjectDNA
dc.subjectdoxorubicin
dc.subjectmicrobial products not classified elsewhere
dc.subjectAcinetobacter baumannii
dc.subjectanimal cell
dc.subjectantineoplastic activity
dc.subjectapoptosis
dc.subjectarticle
dc.subjectBacillus
dc.subjectcancer cell culture
dc.subjectcancer inhibition
dc.subjectCandida tropicalis
dc.subjectcell proliferation
dc.subjectcell structure
dc.subjectconcentration response
dc.subjectcontrolled study
dc.subjectDNA cleavage
dc.subjectDNA fragmentation
dc.subjectdrug cytotoxicity
dc.subjectdrug isolation
dc.subjectdrug potency
dc.subjectdrug screening
dc.subjectdrug specificity
dc.subjectenzyme activation
dc.subjectIC 50
dc.subjectnonhuman
dc.subjectPseudomonas aeruginosa
dc.titleAnticancer and apoptosis-inducing activities of microbial metabolites
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationElectronic Journal of Biotechnology. Vol 13, No.5 (2010), p.-
dc.identifier.doi10.2225/vol13-issue5-fulltext-7
Appears in Collections:Scopus 1983-2021

Files in This Item:
There are no files associated with this item.


Items in SWU repository are protected by copyright, with all rights reserved, unless otherwise indicated.