Interplay between Epigenetics, Expression of Estrogen Receptor- α, HER2/ERBB2 and Sensitivity of Triple Negative Breast Cancer Cells to Hormonal Therapy

Triple negative breast cancer (TNBC) cells are resistant to hormonal/targeted therapies. This study aims to investigate epigenetic differences between TNBC and other types of breast cancer and the effect of epigenetic modulation on the response of TNBC cells to hormonal therapy. Thus, we investigate...

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Main Authors: Wafaa S Ramadan, Cijo George Vazhappilly, Ekram M Saleh, Varsha Menon, Aya M AlAzawi, Ahmed T El-Serafi, Wael Mansour, Raafat El-Awady
Format: Article
Language:English
Published: MDPI AG 2018-12-01
Series:Cancers
Subjects:
Online Access:http://www.mdpi.com/2072-6694/11/1/13
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spelling doaj-9dfbff6c91bb438d9fd35b76f5842bd02020-11-24T23:29:37ZengMDPI AGCancers2072-66942018-12-011111310.3390/cancers11010013cancers11010013Interplay between Epigenetics, Expression of Estrogen Receptor- α, HER2/ERBB2 and Sensitivity of Triple Negative Breast Cancer Cells to Hormonal TherapyWafaa S Ramadan0Cijo George Vazhappilly1Ekram M Saleh2Varsha Menon3Aya M AlAzawi4Ahmed T El-Serafi5Wael Mansour6Raafat El-Awady7Sharjah Institute for Medical Research, University of Sharjah, Sharjah 27272, UAESharjah Institute for Medical Research, University of Sharjah, Sharjah 27272, UAECancer Biology Department, National Cancer Institute, Cairo University, Cairo 11796, EgyptSharjah Institute for Medical Research, University of Sharjah, Sharjah 27272, UAESharjah Institute for Medical Research, University of Sharjah, Sharjah 27272, UAESharjah Institute for Medical Research, University of Sharjah, Sharjah 27272, UAECancer Biology Department, National Cancer Institute, Cairo University, Cairo 11796, EgyptSharjah Institute for Medical Research, University of Sharjah, Sharjah 27272, UAETriple negative breast cancer (TNBC) cells are resistant to hormonal/targeted therapies. This study aims to investigate epigenetic differences between TNBC and other types of breast cancer and the effect of epigenetic modulation on the response of TNBC cells to hormonal therapy. Thus, we investigated (i) the expression of different epigenetic markers, (ii) the effect of epigenetic modifying agents on the expression of ERα and HER2/ERBB2 and (iii) the effect on the response to tamoxifen in four breast cancer cell lines with different hormonal receptor status. Our results revealed a differential expression patterns of epigenetic markers in the four breast cancer cells. In TNBC cells, histone deacetylases (HDAC) 1 and 2 were less expressed, whereas HDACs 4 and 6 were overexpressed. Interestingly, treatment with epigenetic modifiers resulted in (i) a pronounced increase in the expression of ERα and HER2/ERBB2 along with (ii) an increase in the sensitivity of TNBC cells to tamoxifen. Collectively, this study indicates a different epigenetic background for TNBC cells, which represses the expression of ERα and HER2/ERBB2. Furthermore, we provide here the rationale for the use of epigenetic modifiers to enhance the response of TNBC to hormonal therapy through upregulation of ERα.http://www.mdpi.com/2072-6694/11/1/13triple negative breast cancerestrogen receptor alphahuman epidermal growth factor receptor-2epigeneticssuberoylanilide hydroxamic acid2′-deoxy-5-azacytidinetamoxifen
collection DOAJ
language English
format Article
sources DOAJ
author Wafaa S Ramadan
Cijo George Vazhappilly
Ekram M Saleh
Varsha Menon
Aya M AlAzawi
Ahmed T El-Serafi
Wael Mansour
Raafat El-Awady
spellingShingle Wafaa S Ramadan
Cijo George Vazhappilly
Ekram M Saleh
Varsha Menon
Aya M AlAzawi
Ahmed T El-Serafi
Wael Mansour
Raafat El-Awady
Interplay between Epigenetics, Expression of Estrogen Receptor- α, HER2/ERBB2 and Sensitivity of Triple Negative Breast Cancer Cells to Hormonal Therapy
Cancers
triple negative breast cancer
estrogen receptor alpha
human epidermal growth factor receptor-2
epigenetics
suberoylanilide hydroxamic acid
2′-deoxy-5-azacytidine
tamoxifen
author_facet Wafaa S Ramadan
Cijo George Vazhappilly
Ekram M Saleh
Varsha Menon
Aya M AlAzawi
Ahmed T El-Serafi
Wael Mansour
Raafat El-Awady
author_sort Wafaa S Ramadan
title Interplay between Epigenetics, Expression of Estrogen Receptor- α, HER2/ERBB2 and Sensitivity of Triple Negative Breast Cancer Cells to Hormonal Therapy
title_short Interplay between Epigenetics, Expression of Estrogen Receptor- α, HER2/ERBB2 and Sensitivity of Triple Negative Breast Cancer Cells to Hormonal Therapy
title_full Interplay between Epigenetics, Expression of Estrogen Receptor- α, HER2/ERBB2 and Sensitivity of Triple Negative Breast Cancer Cells to Hormonal Therapy
title_fullStr Interplay between Epigenetics, Expression of Estrogen Receptor- α, HER2/ERBB2 and Sensitivity of Triple Negative Breast Cancer Cells to Hormonal Therapy
title_full_unstemmed Interplay between Epigenetics, Expression of Estrogen Receptor- α, HER2/ERBB2 and Sensitivity of Triple Negative Breast Cancer Cells to Hormonal Therapy
title_sort interplay between epigenetics, expression of estrogen receptor- α, her2/erbb2 and sensitivity of triple negative breast cancer cells to hormonal therapy
publisher MDPI AG
series Cancers
issn 2072-6694
publishDate 2018-12-01
description Triple negative breast cancer (TNBC) cells are resistant to hormonal/targeted therapies. This study aims to investigate epigenetic differences between TNBC and other types of breast cancer and the effect of epigenetic modulation on the response of TNBC cells to hormonal therapy. Thus, we investigated (i) the expression of different epigenetic markers, (ii) the effect of epigenetic modifying agents on the expression of ERα and HER2/ERBB2 and (iii) the effect on the response to tamoxifen in four breast cancer cell lines with different hormonal receptor status. Our results revealed a differential expression patterns of epigenetic markers in the four breast cancer cells. In TNBC cells, histone deacetylases (HDAC) 1 and 2 were less expressed, whereas HDACs 4 and 6 were overexpressed. Interestingly, treatment with epigenetic modifiers resulted in (i) a pronounced increase in the expression of ERα and HER2/ERBB2 along with (ii) an increase in the sensitivity of TNBC cells to tamoxifen. Collectively, this study indicates a different epigenetic background for TNBC cells, which represses the expression of ERα and HER2/ERBB2. Furthermore, we provide here the rationale for the use of epigenetic modifiers to enhance the response of TNBC to hormonal therapy through upregulation of ERα.
topic triple negative breast cancer
estrogen receptor alpha
human epidermal growth factor receptor-2
epigenetics
suberoylanilide hydroxamic acid
2′-deoxy-5-azacytidine
tamoxifen
url http://www.mdpi.com/2072-6694/11/1/13
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