Effects of physiological levels of the green tea extract Epigallocatechin gallate (EGCG) on breast cancer cells

Physiological concentrations of the green tea extract EGCG caused growth inhibition in oestrogen receptor α (ERα)-positive MCF7 cells, that was associated with down-regulation of the ERα and reduced insulin-like growth factor (IGF) binding protein-2 (IGFBP-2) abundance and increased protein abundanc...

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Main Authors: Li eZeng, Jeff M P Holly, Claire ePerks
Format: Article
Language:English
Published: Frontiers Media S.A. 2014-05-01
Series:Frontiers in Endocrinology
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fendo.2014.00061/full
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spelling doaj-39d1eb7bc54e45e6a78c1dcf38b30f562020-11-24T23:21:42ZengFrontiers Media S.A.Frontiers in Endocrinology1664-23922014-05-01510.3389/fendo.2014.0006187560Effects of physiological levels of the green tea extract Epigallocatechin gallate (EGCG) on breast cancer cellsLi eZeng0Jeff M P Holly1Claire ePerks2University of BristolUniversity of BristolUniversity of BristolPhysiological concentrations of the green tea extract EGCG caused growth inhibition in oestrogen receptor α (ERα)-positive MCF7 cells, that was associated with down-regulation of the ERα and reduced insulin-like growth factor (IGF) binding protein-2 (IGFBP-2) abundance and increased protein abundance of the tumour suppressor genes p53/p21. In contrast to MCF7 cells that have wt p53, EGCG alone did not change cell proliferation or death significantly in another ERα-positive cell line T47D that possesses mutant p53. EGCG increased ERα protein levels and as a consequence, the cells responded significantly better to an ERα antagonist Tamoxifen (TAM)) in the presence of EGCG. EGCG significantly increased cell death in an ERα-negative cell line, MDA-MB-231 that also possesses mutant p53. EGCG significantly increased the ERα and IGF-I receptor (IGF-IR) levels and thereby enhanced the sensitivities of the cells to Tamoxifen and a blocking antibody targeting the IGF-1R (αIR3). In contrast to MCF7, T47D and MDA-MB-231 breast cancer cells that exhibited significant changes in key molecules involved in breast growth and survival upon treatment with physiological levels of EGCG, the growth, survival and levels of these proteins in non-malignant breast epithelial cells, MCF10A cells, were not affected.http://journal.frontiersin.org/Journal/10.3389/fendo.2014.00061/fullbreast cancerEGCGphysiologicalgreen teadrug sensitivity
collection DOAJ
language English
format Article
sources DOAJ
author Li eZeng
Jeff M P Holly
Claire ePerks
spellingShingle Li eZeng
Jeff M P Holly
Claire ePerks
Effects of physiological levels of the green tea extract Epigallocatechin gallate (EGCG) on breast cancer cells
Frontiers in Endocrinology
breast cancer
EGCG
physiological
green tea
drug sensitivity
author_facet Li eZeng
Jeff M P Holly
Claire ePerks
author_sort Li eZeng
title Effects of physiological levels of the green tea extract Epigallocatechin gallate (EGCG) on breast cancer cells
title_short Effects of physiological levels of the green tea extract Epigallocatechin gallate (EGCG) on breast cancer cells
title_full Effects of physiological levels of the green tea extract Epigallocatechin gallate (EGCG) on breast cancer cells
title_fullStr Effects of physiological levels of the green tea extract Epigallocatechin gallate (EGCG) on breast cancer cells
title_full_unstemmed Effects of physiological levels of the green tea extract Epigallocatechin gallate (EGCG) on breast cancer cells
title_sort effects of physiological levels of the green tea extract epigallocatechin gallate (egcg) on breast cancer cells
publisher Frontiers Media S.A.
series Frontiers in Endocrinology
issn 1664-2392
publishDate 2014-05-01
description Physiological concentrations of the green tea extract EGCG caused growth inhibition in oestrogen receptor α (ERα)-positive MCF7 cells, that was associated with down-regulation of the ERα and reduced insulin-like growth factor (IGF) binding protein-2 (IGFBP-2) abundance and increased protein abundance of the tumour suppressor genes p53/p21. In contrast to MCF7 cells that have wt p53, EGCG alone did not change cell proliferation or death significantly in another ERα-positive cell line T47D that possesses mutant p53. EGCG increased ERα protein levels and as a consequence, the cells responded significantly better to an ERα antagonist Tamoxifen (TAM)) in the presence of EGCG. EGCG significantly increased cell death in an ERα-negative cell line, MDA-MB-231 that also possesses mutant p53. EGCG significantly increased the ERα and IGF-I receptor (IGF-IR) levels and thereby enhanced the sensitivities of the cells to Tamoxifen and a blocking antibody targeting the IGF-1R (αIR3). In contrast to MCF7, T47D and MDA-MB-231 breast cancer cells that exhibited significant changes in key molecules involved in breast growth and survival upon treatment with physiological levels of EGCG, the growth, survival and levels of these proteins in non-malignant breast epithelial cells, MCF10A cells, were not affected.
topic breast cancer
EGCG
physiological
green tea
drug sensitivity
url http://journal.frontiersin.org/Journal/10.3389/fendo.2014.00061/full
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