Nordamnacanthal potentiates the cytotoxic effects of tamoxifen in human breast cancer cells

Tamoxifen (TAM) is the mainline drug treatment for breast cancer, despite its side effects and the development of resistance. As an alternative approach, in the present study a novel combination therapy was established through combining TAM with nordamnacanthal (NDAM) in order to investigate the add...

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Main Authors: Mohamed Alitheen, Noorjahan Banu, Nik Abd Rahman, Nik Mohd Afizan, Ho, Chai Ling, Subramani, Tamilselvan, Osman, Che Puteh, Ismail, Nor Hadiani, Swee, Keong Yeap, Wan, Yang Ho
Format: Article
Language:English
Published: Spandidos Publications 2015
Online Access:http://psasir.upm.edu.my/id/eprint/45610/1/CANCER.pdf
http://psasir.upm.edu.my/id/eprint/45610/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4247001/
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spelling my.upm.eprints.456102021-01-23T22:07:19Z http://psasir.upm.edu.my/id/eprint/45610/ Nordamnacanthal potentiates the cytotoxic effects of tamoxifen in human breast cancer cells Mohamed Alitheen, Noorjahan Banu Nik Abd Rahman, Nik Mohd Afizan Ho, Chai Ling Subramani, Tamilselvan Osman, Che Puteh Ismail, Nor Hadiani Swee, Keong Yeap Wan, Yang Ho Tamoxifen (TAM) is the mainline drug treatment for breast cancer, despite its side effects and the development of resistance. As an alternative approach, in the present study a novel combination therapy was established through combining TAM with nordamnacanthal (NDAM) in order to investigate the additive effect of these drugs in MCF-7 human breast cancer cells. A significant dose-dependent reduction in cell viability and an increase in apoptosis were observed in the MCF-7 cells cotreated with TAM and NDAM compared with the untreated control cells or the cells treated with TAM and NDAM alone (P<0.05). The cytotoxic influence of the combination of TAM and NDAM was found to be two-fold that of the individual agents. Annexin V/propidium iodide double-staining revealed the typical nuclear features of apoptosis. Furthermore, an increase in the proportion of apoptotic, Annexin V-positive cells was observed with the combination therapy. Moreover, this apoptotic induction was associated with a collapse of the mitochondrial membrane potential and the generation of reactive oxygen species. To the best of our knowledge, the findings of the present study are the first to suggest that combining TAM with NDAM may be a potential combination therapy for the treatment of breast cancer and may have the potential to minimize or eliminate the side effects associated with high doses of TAM. Spandidos Publications 2015 Article PeerReviewed text en http://psasir.upm.edu.my/id/eprint/45610/1/CANCER.pdf Mohamed Alitheen, Noorjahan Banu and Nik Abd Rahman, Nik Mohd Afizan and Ho, Chai Ling and Subramani, Tamilselvan and Osman, Che Puteh and Ismail, Nor Hadiani and Swee, Keong Yeap and Wan, Yang Ho (2015) Nordamnacanthal potentiates the cytotoxic effects of tamoxifen in human breast cancer cells. Oncology Letters, 9 (1). pp. 335-340. ISSN 1792-1082; ESSN: 1792-1074 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4247001/ 10.3892/ol.2014.2697
institution Universiti Putra Malaysia
building UPM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Putra Malaysia
content_source UPM Institutional Repository
url_provider http://psasir.upm.edu.my/
language English
description Tamoxifen (TAM) is the mainline drug treatment for breast cancer, despite its side effects and the development of resistance. As an alternative approach, in the present study a novel combination therapy was established through combining TAM with nordamnacanthal (NDAM) in order to investigate the additive effect of these drugs in MCF-7 human breast cancer cells. A significant dose-dependent reduction in cell viability and an increase in apoptosis were observed in the MCF-7 cells cotreated with TAM and NDAM compared with the untreated control cells or the cells treated with TAM and NDAM alone (P<0.05). The cytotoxic influence of the combination of TAM and NDAM was found to be two-fold that of the individual agents. Annexin V/propidium iodide double-staining revealed the typical nuclear features of apoptosis. Furthermore, an increase in the proportion of apoptotic, Annexin V-positive cells was observed with the combination therapy. Moreover, this apoptotic induction was associated with a collapse of the mitochondrial membrane potential and the generation of reactive oxygen species. To the best of our knowledge, the findings of the present study are the first to suggest that combining TAM with NDAM may be a potential combination therapy for the treatment of breast cancer and may have the potential to minimize or eliminate the side effects associated with high doses of TAM.
format Article
author Mohamed Alitheen, Noorjahan Banu
Nik Abd Rahman, Nik Mohd Afizan
Ho, Chai Ling
Subramani, Tamilselvan
Osman, Che Puteh
Ismail, Nor Hadiani
Swee, Keong Yeap
Wan, Yang Ho
spellingShingle Mohamed Alitheen, Noorjahan Banu
Nik Abd Rahman, Nik Mohd Afizan
Ho, Chai Ling
Subramani, Tamilselvan
Osman, Che Puteh
Ismail, Nor Hadiani
Swee, Keong Yeap
Wan, Yang Ho
Nordamnacanthal potentiates the cytotoxic effects of tamoxifen in human breast cancer cells
author_facet Mohamed Alitheen, Noorjahan Banu
Nik Abd Rahman, Nik Mohd Afizan
Ho, Chai Ling
Subramani, Tamilselvan
Osman, Che Puteh
Ismail, Nor Hadiani
Swee, Keong Yeap
Wan, Yang Ho
author_sort Mohamed Alitheen, Noorjahan Banu
title Nordamnacanthal potentiates the cytotoxic effects of tamoxifen in human breast cancer cells
title_short Nordamnacanthal potentiates the cytotoxic effects of tamoxifen in human breast cancer cells
title_full Nordamnacanthal potentiates the cytotoxic effects of tamoxifen in human breast cancer cells
title_fullStr Nordamnacanthal potentiates the cytotoxic effects of tamoxifen in human breast cancer cells
title_full_unstemmed Nordamnacanthal potentiates the cytotoxic effects of tamoxifen in human breast cancer cells
title_sort nordamnacanthal potentiates the cytotoxic effects of tamoxifen in human breast cancer cells
publisher Spandidos Publications
publishDate 2015
url http://psasir.upm.edu.my/id/eprint/45610/1/CANCER.pdf
http://psasir.upm.edu.my/id/eprint/45610/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4247001/
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