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Combined xanthorrhizol-curcumin exhibits synergistic growth inhibitory activity via apoptosis induction in human breast cancer cells MDA-MB-231

BACKGROUND: It has been suggested that combined effect of natural products may improve the treatment effectiveness in combating proliferation of cancer cells. The present study was undertaken to evaluate the possibility that the combination of xanthorrhizol and curcumin might show synergistic growth...

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Autores principales: Cheah, Yew Hoong, Nordin, Fariza Juliana, Sarip, Rozie, Tee, Thiam Tsui, Azimahtol, Hawariah Lope Pihie, Sirat, Hasnah M, Rashid, Badrul Amini Abd, Abdullah, Noor Rain, Ismail, Zakiah
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2630298/
https://www.ncbi.nlm.nih.gov/pubmed/19118501
http://dx.doi.org/10.1186/1475-2867-9-1
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author Cheah, Yew Hoong
Nordin, Fariza Juliana
Sarip, Rozie
Tee, Thiam Tsui
Azimahtol, Hawariah Lope Pihie
Sirat, Hasnah M
Rashid, Badrul Amini Abd
Abdullah, Noor Rain
Ismail, Zakiah
author_facet Cheah, Yew Hoong
Nordin, Fariza Juliana
Sarip, Rozie
Tee, Thiam Tsui
Azimahtol, Hawariah Lope Pihie
Sirat, Hasnah M
Rashid, Badrul Amini Abd
Abdullah, Noor Rain
Ismail, Zakiah
author_sort Cheah, Yew Hoong
collection PubMed
description BACKGROUND: It has been suggested that combined effect of natural products may improve the treatment effectiveness in combating proliferation of cancer cells. The present study was undertaken to evaluate the possibility that the combination of xanthorrhizol and curcumin might show synergistic growth inhibitory effect towards MDA-MB-231 human breast cancer cells via apoptosis induction. The effective dose that produced 50% growth inhibition (GI(50)) was calculated from the log dose-response curve of fixed-combinations of xanthorrhizol and curcumin generated from the sulforhodamine B (SRB) assay. The experimental GI(50 )value was used to determine the synergistic activity of the combination treatment by isobolographic analysis and combination-index method. Further investigation of mode of cell death induced by the combination treatment was conducted in the present study. RESULTS: Isobole analysis revealed that substances interaction was synergistic when xanthorrhizol and curcumin were added concurrently to the cultures but merely additive when they were added sequentially. The synergistic combination treatment was then applied to the cultures to investigate the mode of cell death induced by the treatment. Immunofluorescence staining using antibody MitoCapture™ revealed the possibility of altered mitochondrial transmembrane potential, which is one of the hallmark of apoptosis. Hoechst 33258 nuclear staining assay showed the rate of apoptosis of MDA-MB-231 cells to increase in response to the treatment. Apoptotic cell death was further confirmed by DNA fragmentation assay, where internucleosomal excision of DNA was induced upon treatment with xanthorrhizol-curcumin. CONCLUSION: This is the first time the combined cytotoxic effect of xanthorrhizol and curcumin on MDA-MB-231 cells has been documented and our findings provide experimental support to the hypothesis that combined xanthorrhizol-curcumin showed synergistic growth inhibitory activity on MDA-MB-231 cells via apoptosis induction.
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spelling pubmed-26302982009-01-24 Combined xanthorrhizol-curcumin exhibits synergistic growth inhibitory activity via apoptosis induction in human breast cancer cells MDA-MB-231 Cheah, Yew Hoong Nordin, Fariza Juliana Sarip, Rozie Tee, Thiam Tsui Azimahtol, Hawariah Lope Pihie Sirat, Hasnah M Rashid, Badrul Amini Abd Abdullah, Noor Rain Ismail, Zakiah Cancer Cell Int Primary Research BACKGROUND: It has been suggested that combined effect of natural products may improve the treatment effectiveness in combating proliferation of cancer cells. The present study was undertaken to evaluate the possibility that the combination of xanthorrhizol and curcumin might show synergistic growth inhibitory effect towards MDA-MB-231 human breast cancer cells via apoptosis induction. The effective dose that produced 50% growth inhibition (GI(50)) was calculated from the log dose-response curve of fixed-combinations of xanthorrhizol and curcumin generated from the sulforhodamine B (SRB) assay. The experimental GI(50 )value was used to determine the synergistic activity of the combination treatment by isobolographic analysis and combination-index method. Further investigation of mode of cell death induced by the combination treatment was conducted in the present study. RESULTS: Isobole analysis revealed that substances interaction was synergistic when xanthorrhizol and curcumin were added concurrently to the cultures but merely additive when they were added sequentially. The synergistic combination treatment was then applied to the cultures to investigate the mode of cell death induced by the treatment. Immunofluorescence staining using antibody MitoCapture™ revealed the possibility of altered mitochondrial transmembrane potential, which is one of the hallmark of apoptosis. Hoechst 33258 nuclear staining assay showed the rate of apoptosis of MDA-MB-231 cells to increase in response to the treatment. Apoptotic cell death was further confirmed by DNA fragmentation assay, where internucleosomal excision of DNA was induced upon treatment with xanthorrhizol-curcumin. CONCLUSION: This is the first time the combined cytotoxic effect of xanthorrhizol and curcumin on MDA-MB-231 cells has been documented and our findings provide experimental support to the hypothesis that combined xanthorrhizol-curcumin showed synergistic growth inhibitory activity on MDA-MB-231 cells via apoptosis induction. BioMed Central 2009-01-02 /pmc/articles/PMC2630298/ /pubmed/19118501 http://dx.doi.org/10.1186/1475-2867-9-1 Text en Copyright © 2009 Cheah et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Primary Research
Cheah, Yew Hoong
Nordin, Fariza Juliana
Sarip, Rozie
Tee, Thiam Tsui
Azimahtol, Hawariah Lope Pihie
Sirat, Hasnah M
Rashid, Badrul Amini Abd
Abdullah, Noor Rain
Ismail, Zakiah
Combined xanthorrhizol-curcumin exhibits synergistic growth inhibitory activity via apoptosis induction in human breast cancer cells MDA-MB-231
title Combined xanthorrhizol-curcumin exhibits synergistic growth inhibitory activity via apoptosis induction in human breast cancer cells MDA-MB-231
title_full Combined xanthorrhizol-curcumin exhibits synergistic growth inhibitory activity via apoptosis induction in human breast cancer cells MDA-MB-231
title_fullStr Combined xanthorrhizol-curcumin exhibits synergistic growth inhibitory activity via apoptosis induction in human breast cancer cells MDA-MB-231
title_full_unstemmed Combined xanthorrhizol-curcumin exhibits synergistic growth inhibitory activity via apoptosis induction in human breast cancer cells MDA-MB-231
title_short Combined xanthorrhizol-curcumin exhibits synergistic growth inhibitory activity via apoptosis induction in human breast cancer cells MDA-MB-231
title_sort combined xanthorrhizol-curcumin exhibits synergistic growth inhibitory activity via apoptosis induction in human breast cancer cells mda-mb-231
topic Primary Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2630298/
https://www.ncbi.nlm.nih.gov/pubmed/19118501
http://dx.doi.org/10.1186/1475-2867-9-1
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