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Conference Paper: Bivariate flow cytometric analysis of hl-60 cell cycle progression affected by polysaccharopeptide (psp) from coriolus versicolor mycelia
Title | Bivariate flow cytometric analysis of hl-60 cell cycle progression affected by polysaccharopeptide (psp) from coriolus versicolor mycelia |
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Authors | |
Issue Date | 2004 |
Publisher | Wiley |
Citation | ISAC XXII International Congress, Montpellier, France, 22-27 May 2004. In Cytometry, 2004, v. 59A n. 1, p. 118-119 How to Cite? |
Abstract | Introduction: Anticancer agents generally target on cancer cells either by alter-ation of their cell cycle or induction of apoptosis or necrosis. The polysaccha-ropeptide (PSP)(I’m-Yunity™) isolated from the fermented mycelia of fungusCoriolus versicolor Cov-1™ strain exerts potent activity on inhibition of cell pro-liferation in a wide range of malignancies. However, whether the anticancermechanism(s) of PSP involves alteration of cell cycle is still not clear. The spe-cific aim of this study was to apply 5-bromodeoxyuridine (BrdUrd) to pulse labelactive synthesizing DNA to investigate the effect of PSP on cell cycle kinetics onhuman promyelocytic leukemic HL-60 cells. Methods: HL-60 cells were pulse-labeled with BrdUrd, treated with and without PSP (25, 400 _g/ml), and sampledat certain time intervals. The cell cycle kinetics was studied by usingBrdUrd/Propidium iodide (PI) bivariate flow cytometric analysis. Results: Theresults revealed that high dose of PSP reduced cells in G0/G1 phase, accumulat-ed cells in both S and G2/M phase. The DNA synthesis time and cancer potentialdoubling time was significantly extended in the HL-60 cells after PSP treatment.Conclusion: PSP retards cancer growth via elongation on the S phase, slows thecells returning to G1 from G2/M. Our data indicate that the interference on cellcycle progression is part of the anticancer mechanism(s) of PSP. |
Persistent Identifier | http://hdl.handle.net/10722/110282 |
ISSN |
DC Field | Value | Language |
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dc.contributor.author | Wan, JMF | en_HK |
dc.contributor.author | Yang, X | en_HK |
dc.contributor.author | Sit, WH | en_HK |
dc.date.accessioned | 2010-09-26T01:59:09Z | - |
dc.date.available | 2010-09-26T01:59:09Z | - |
dc.date.issued | 2004 | en_HK |
dc.identifier.citation | ISAC XXII International Congress, Montpellier, France, 22-27 May 2004. In Cytometry, 2004, v. 59A n. 1, p. 118-119 | - |
dc.identifier.issn | 0196-4763 | - |
dc.identifier.uri | http://hdl.handle.net/10722/110282 | - |
dc.description.abstract | Introduction: Anticancer agents generally target on cancer cells either by alter-ation of their cell cycle or induction of apoptosis or necrosis. The polysaccha-ropeptide (PSP)(I’m-Yunity™) isolated from the fermented mycelia of fungusCoriolus versicolor Cov-1™ strain exerts potent activity on inhibition of cell pro-liferation in a wide range of malignancies. However, whether the anticancermechanism(s) of PSP involves alteration of cell cycle is still not clear. The spe-cific aim of this study was to apply 5-bromodeoxyuridine (BrdUrd) to pulse labelactive synthesizing DNA to investigate the effect of PSP on cell cycle kinetics onhuman promyelocytic leukemic HL-60 cells. Methods: HL-60 cells were pulse-labeled with BrdUrd, treated with and without PSP (25, 400 _g/ml), and sampledat certain time intervals. The cell cycle kinetics was studied by usingBrdUrd/Propidium iodide (PI) bivariate flow cytometric analysis. Results: Theresults revealed that high dose of PSP reduced cells in G0/G1 phase, accumulat-ed cells in both S and G2/M phase. The DNA synthesis time and cancer potentialdoubling time was significantly extended in the HL-60 cells after PSP treatment.Conclusion: PSP retards cancer growth via elongation on the S phase, slows thecells returning to G1 from G2/M. Our data indicate that the interference on cellcycle progression is part of the anticancer mechanism(s) of PSP. | - |
dc.language | eng | en_HK |
dc.publisher | Wiley | - |
dc.relation.ispartof | Cytometry | en_HK |
dc.title | Bivariate flow cytometric analysis of hl-60 cell cycle progression affected by polysaccharopeptide (psp) from coriolus versicolor mycelia | en_HK |
dc.type | Conference_Paper | en_HK |
dc.identifier.email | Sit, WH: whsit@HKUCC.hku.hk | en_HK |
dc.identifier.email | Wan, JMF: jmfwan@hkusua.hku.hk | en_HK |
dc.identifier.authority | Wan, JMF=rp00798 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1002/cyto.a.20046.abs | - |
dc.identifier.hkuros | 104588 | en_HK |
dc.identifier.issnl | 0196-4763 | - |