Vitamin C suppresses cell death in MCF-7 human breast cancer cells induced by tamoxifen

Vitamin C is generally thought to enhance immunity and is widely taken as a supplement especially during cancer treatment. Tamoxifen (TAM) has both cytostatic and cytotoxic properties for breast cancer. TAM engaged mitochondrial oestrogen receptor beta in MCF-7 cells and induces apoptosis by activat...

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Main Authors: Subramani, Tamilselvan, Yeap, Swee Keong, Ho, Wan Yang, Ho, Chai Ling, Omar, Abdul Rahman, Abdul Aziz, Suraini, Nik Abd. Rahman, Nik Mohd. Afizan, Mohamed Alitheen, Noorjahan Banu
Format: Article
Published: Wiley-Blackwell Publishing 2014
Online Access:http://psasir.upm.edu.my/id/eprint/35992/
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author Subramani, Tamilselvan
Yeap, Swee Keong
Ho, Wan Yang
Ho, Chai Ling
Omar, Abdul Rahman
Abdul Aziz, Suraini
Nik Abd. Rahman, Nik Mohd. Afizan
Mohamed Alitheen, Noorjahan Banu
author_facet Subramani, Tamilselvan
Yeap, Swee Keong
Ho, Wan Yang
Ho, Chai Ling
Omar, Abdul Rahman
Abdul Aziz, Suraini
Nik Abd. Rahman, Nik Mohd. Afizan
Mohamed Alitheen, Noorjahan Banu
author_sort Subramani, Tamilselvan
building UPM Institutional Repository
collection Online Access
description Vitamin C is generally thought to enhance immunity and is widely taken as a supplement especially during cancer treatment. Tamoxifen (TAM) has both cytostatic and cytotoxic properties for breast cancer. TAM engaged mitochondrial oestrogen receptor beta in MCF-7 cells and induces apoptosis by activation of pro-caspase-8 followed by downstream events, including an increase in reactive oxygen species and the release of pro-apoptotic factors from the mitochondria. In addition to that, TAM binds with high affinity to the microsomal anti-oestrogen-binding site and inhibits cholesterol esterification at therapeutic doses. This study aimed to investigate the role of vitamin C in TAM-mediated apoptosis. Cells were loaded with vitamin C by exposure to dehydroascorbic acid, thereby circumventing in vitro artefacts associated with the poor transport and pro-oxidant effects of ascorbic acid. Pre-treatment with vitamin C caused a dose-dependent attenuation of cytotoxicity, as measured by acridine-orange/propidium iodide (AO/PI) and Annexin V assay after treatment with TAM. Vitamin C dose-dependently protected cancer cells against lipid peroxidation caused by TAM treatment. By real-time PCR analysis, an impressive increase in FasL and tumour necrosis factor-α (TNF-α) mRNA was detected after TAM treatment. In addition, a decrease in mitochondrial transmembrane potential was observed. These results support the hypothesis that vitamin C supplementation during cancer treatment may detrimentally affect therapeutic response.
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spelling upm-359922016-02-12T07:21:54Z http://psasir.upm.edu.my/id/eprint/35992/ Vitamin C suppresses cell death in MCF-7 human breast cancer cells induced by tamoxifen Subramani, Tamilselvan Yeap, Swee Keong Ho, Wan Yang Ho, Chai Ling Omar, Abdul Rahman Abdul Aziz, Suraini Nik Abd. Rahman, Nik Mohd. Afizan Mohamed Alitheen, Noorjahan Banu Vitamin C is generally thought to enhance immunity and is widely taken as a supplement especially during cancer treatment. Tamoxifen (TAM) has both cytostatic and cytotoxic properties for breast cancer. TAM engaged mitochondrial oestrogen receptor beta in MCF-7 cells and induces apoptosis by activation of pro-caspase-8 followed by downstream events, including an increase in reactive oxygen species and the release of pro-apoptotic factors from the mitochondria. In addition to that, TAM binds with high affinity to the microsomal anti-oestrogen-binding site and inhibits cholesterol esterification at therapeutic doses. This study aimed to investigate the role of vitamin C in TAM-mediated apoptosis. Cells were loaded with vitamin C by exposure to dehydroascorbic acid, thereby circumventing in vitro artefacts associated with the poor transport and pro-oxidant effects of ascorbic acid. Pre-treatment with vitamin C caused a dose-dependent attenuation of cytotoxicity, as measured by acridine-orange/propidium iodide (AO/PI) and Annexin V assay after treatment with TAM. Vitamin C dose-dependently protected cancer cells against lipid peroxidation caused by TAM treatment. By real-time PCR analysis, an impressive increase in FasL and tumour necrosis factor-α (TNF-α) mRNA was detected after TAM treatment. In addition, a decrease in mitochondrial transmembrane potential was observed. These results support the hypothesis that vitamin C supplementation during cancer treatment may detrimentally affect therapeutic response. Wiley-Blackwell Publishing 2014-02 Article PeerReviewed Subramani, Tamilselvan and Yeap, Swee Keong and Ho, Wan Yang and Ho, Chai Ling and Omar, Abdul Rahman and Abdul Aziz, Suraini and Nik Abd. Rahman, Nik Mohd. Afizan and Mohamed Alitheen, Noorjahan Banu (2014) Vitamin C suppresses cell death in MCF-7 human breast cancer cells induced by tamoxifen. Journal of Cellular and Molecular Medicine, 18 (2). pp. 305-313. ISSN 1582-1838; ESSN: 1582-4934 http://onlinelibrary.wiley.com/doi/10.1111/jcmm.12188/abstract 10.1111/jcmm.12188
spellingShingle Subramani, Tamilselvan
Yeap, Swee Keong
Ho, Wan Yang
Ho, Chai Ling
Omar, Abdul Rahman
Abdul Aziz, Suraini
Nik Abd. Rahman, Nik Mohd. Afizan
Mohamed Alitheen, Noorjahan Banu
Vitamin C suppresses cell death in MCF-7 human breast cancer cells induced by tamoxifen
title Vitamin C suppresses cell death in MCF-7 human breast cancer cells induced by tamoxifen
title_full Vitamin C suppresses cell death in MCF-7 human breast cancer cells induced by tamoxifen
title_fullStr Vitamin C suppresses cell death in MCF-7 human breast cancer cells induced by tamoxifen
title_full_unstemmed Vitamin C suppresses cell death in MCF-7 human breast cancer cells induced by tamoxifen
title_short Vitamin C suppresses cell death in MCF-7 human breast cancer cells induced by tamoxifen
title_sort vitamin c suppresses cell death in mcf-7 human breast cancer cells induced by tamoxifen
url http://psasir.upm.edu.my/id/eprint/35992/
http://psasir.upm.edu.my/id/eprint/35992/
http://psasir.upm.edu.my/id/eprint/35992/