File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Involvement of NF-κB and c-myc signaling pathways in the apoptosis of HL-60 cells induced by alkaloids of Tripterygium hypoglaucum (levl.) Hutch

TitleInvolvement of NF-κB and c-myc signaling pathways in the apoptosis of HL-60 cells induced by alkaloids of Tripterygium hypoglaucum (levl.) Hutch
Authors
KeywordsApoptosis
CDNA microarray
Cytotoxicity
Tripterygium hypoglaucum (levl.) Hutch extracts
Issue Date2004
PublisherUrban und Fischer Verlag. The Journal's web site is located at http://www.elsevier.com/locate/phytomed
Citation
Phytomedicine, 2004, v. 11 n. 4, p. 295-302 How to Cite?
AbstractTripterygium hypoglaucum (levl.) Hutch (Celastraceae) (THH) root is a Chinese medicinal herb commonly used for treating autoimmune diseases. In the present study, alkaloids of THH were prepared and their cytotoxicity against the HL-60 cell was investigated. THH-induced apoptosis was observed using flow cytometry, confocal fluorescence microscope, and DNA laddering and caspase assays. The molecular mechanism involved in the induction of HL-60 cell apoptosis by THH alkaloids was examined using cDNA microarrays containing 3000 human genes derived from a leukocyte cDNA library. Sixteen genes were identified to be differentially expressed in HL-60 cells upon THH treatment. Several genes related to the NF-κB signaling pathway and cell apoptosis (such as NFKBIB, PRG1 and B2M) were up-regulated. In addition, c-myc binding protein and apoptosis-related cysteine proteases caspase-3 and caspase-8 were also regulated. The changes in c-Myc RNA expression and c-myc protein level were further confirmed by RT-PCR and Western blot analysis. The results demonstrated that THH alkaloids induced apoptosis of HL-60 cells though c-myc and NF-κB signaling pathways.
Persistent Identifierhttp://hdl.handle.net/10722/167954
ISSN
2021 Impact Factor: 6.656
2020 SCImago Journal Rankings: 1.045
ISI Accession Number ID
References

 

DC FieldValueLanguage
dc.contributor.authorZhuang, WJen_US
dc.contributor.authorFong, CCen_US
dc.contributor.authorCao, Jen_US
dc.contributor.authorAo, Len_US
dc.contributor.authorLeung, CHen_US
dc.contributor.authorCheung, HYen_US
dc.contributor.authorXiao, PGen_US
dc.contributor.authorFong, WFen_US
dc.contributor.authorYang, MSen_US
dc.date.accessioned2012-10-08T03:13:22Z-
dc.date.available2012-10-08T03:13:22Z-
dc.date.issued2004en_US
dc.identifier.citationPhytomedicine, 2004, v. 11 n. 4, p. 295-302en_US
dc.identifier.issn0944-7113en_US
dc.identifier.urihttp://hdl.handle.net/10722/167954-
dc.description.abstractTripterygium hypoglaucum (levl.) Hutch (Celastraceae) (THH) root is a Chinese medicinal herb commonly used for treating autoimmune diseases. In the present study, alkaloids of THH were prepared and their cytotoxicity against the HL-60 cell was investigated. THH-induced apoptosis was observed using flow cytometry, confocal fluorescence microscope, and DNA laddering and caspase assays. The molecular mechanism involved in the induction of HL-60 cell apoptosis by THH alkaloids was examined using cDNA microarrays containing 3000 human genes derived from a leukocyte cDNA library. Sixteen genes were identified to be differentially expressed in HL-60 cells upon THH treatment. Several genes related to the NF-κB signaling pathway and cell apoptosis (such as NFKBIB, PRG1 and B2M) were up-regulated. In addition, c-myc binding protein and apoptosis-related cysteine proteases caspase-3 and caspase-8 were also regulated. The changes in c-Myc RNA expression and c-myc protein level were further confirmed by RT-PCR and Western blot analysis. The results demonstrated that THH alkaloids induced apoptosis of HL-60 cells though c-myc and NF-κB signaling pathways.en_US
dc.languageengen_US
dc.publisherUrban und Fischer Verlag. The Journal's web site is located at http://www.elsevier.com/locate/phytomeden_US
dc.relation.ispartofPhytomedicineen_US
dc.subjectApoptosis-
dc.subjectCDNA microarray-
dc.subjectCytotoxicity-
dc.subjectTripterygium hypoglaucum (levl.) Hutch extracts-
dc.subject.meshAntineoplastic Agents, Phytogenic - Administration & Dosage - Pharmacology - Therapeutic Useen_US
dc.subject.meshApoptosis - Drug Effectsen_US
dc.subject.meshBlotting, Westernen_US
dc.subject.meshDna, Neoplasm - Drug Effectsen_US
dc.subject.meshFlow Cytometryen_US
dc.subject.meshHl-60 Cells - Drug Effectsen_US
dc.subject.meshHumansen_US
dc.subject.meshMicroscopy, Confocalen_US
dc.subject.meshNf-Kappa B - Metabolismen_US
dc.subject.meshPhytotherapyen_US
dc.subject.meshPlant Extracts - Administration & Dosage - Pharmacology - Therapeutic Useen_US
dc.subject.meshPlant Rootsen_US
dc.subject.meshProto-Oncogene Proteins C-Myc - Metabolismen_US
dc.subject.meshReverse Transcriptase Polymerase Chain Reactionen_US
dc.subject.meshTripterygiumen_US
dc.titleInvolvement of NF-κB and c-myc signaling pathways in the apoptosis of HL-60 cells induced by alkaloids of Tripterygium hypoglaucum (levl.) Hutchen_US
dc.typeArticleen_US
dc.identifier.emailLeung, CH:duncanl@hkucc.hku.hken_US
dc.identifier.authorityLeung, CH=rp00730en_US
dc.description.naturelink_to_subscribed_fulltexten_US
dc.identifier.doi10.1078/0944711041495128en_US
dc.identifier.pmid15185841-
dc.identifier.scopuseid_2-s2.0-2442637447en_US
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-2442637447&selection=ref&src=s&origin=recordpageen_US
dc.identifier.volume11en_US
dc.identifier.issue4en_US
dc.identifier.spage295en_US
dc.identifier.epage302en_US
dc.identifier.isiWOS:000221891400003-
dc.publisher.placeGermanyen_US
dc.identifier.scopusauthoridZhuang, WJ=7103154978en_US
dc.identifier.scopusauthoridFong, CC=11739503800en_US
dc.identifier.scopusauthoridCao, J=26643166500en_US
dc.identifier.scopusauthoridAo, L=15055316500en_US
dc.identifier.scopusauthoridLeung, CH=7402612570en_US
dc.identifier.scopusauthoridCheung, HY=7201839371en_US
dc.identifier.scopusauthoridXiao, PG=7103088959en_US
dc.identifier.scopusauthoridFong, WF=7102816013en_US
dc.identifier.scopusauthoridYang, MS=7404925734en_US
dc.identifier.citeulike17692-
dc.identifier.issnl0944-7113-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats