In vitro mechanism for downregulation of ER-α expression by epigallocatechin gallate in ER+/PR+ human breast cancer cells.
In vitro mechanism for downregulation of ER-α expression by epigallocatechin gallate in ER+/PR+ human breast cancer cells.
复制标题
DOI:
10.1002/mnfr.201200560
复制
发表时间:
2013-05
影响因子:
5.2
通讯作者:
Andò S
中科院分区:
文献类型:
--
作者:
De Amicis F;Russo A;Avena P;Santoro M;Vivacqua A;Bonofiglio D;Mauro L;Aquila S;Tramontano D;Fuqua SA;Andò S
Exposure of the breast to estrogens and other sex hormones is an important cancer risk factor and estrogen receptor down-regulators are attracting significant clinical interest. Epigallocatechin gallate (EGCG), a polyphenolic compound found in green tea, has gained considerable attention for its antitumor properties. Here we aimed to investigate the molecular mechanisms through which EGCG regulates ERα expression in ER+ PR+ breast cancer cells. Western blotting analysis, real time PCR and transient transfections of deletion fragments of the ERα gene promoter show that EGCG down-regulates ERα protein, mRNA and gene promoter activity with a concomitant reduction of ERα genomic and non genomic signal. These events occur through p38MAPK/CK2 activation, causing the release from Hsp90 of PR-B and its consequent nuclear translocation as evidenced by immunofluorescence studies. EMSA and ChIP assay reveal that, upon EGCG treatment, PR-B is recruited at the half PRE site on ERα promoter. This is concomitant with the formation of a corepressor complex containing NCoR and HDAC1 while RNA polymerase II is displaced. The events are crucially mediated by PR-B isoform, since they are abrogated with PR-B siRNA. Our data provide evidence for a mechanism by which EGCG down-regulates ERα and explain the inhibitory action of EGCG on the proliferation of ER+ PR+ cancer cells tested. We suggest that the EGCG/PR-B signaling should be further exploited for clinical approach.