The histone deacetylase inhibitor trichostatin A sensitizes estrogen receptor alpha-negative breast cancer cells to tamoxifen.
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Interaction of TFAP2C with the estrogen receptor-alpha promoter is controlled by chromatin structureCircadian disruption and breast cancer: an epigenetic link?Specific activity of class II histone deacetylases in human breast cancer cells5-Aza-2-deoxycytidine and trichostatin A increase COUP-TFII expression in antiestrogen-resistant breast cancer cell lines.Minireview: The versatile roles of lysine deacetylases in steroid receptor signalingZ-ligustilide restores tamoxifen sensitivity of ERa negative breast cancer cells by reversing MTA1/IFI16/HDACs complex mediated epigenetic repression of ERaATM modulates transcription in response to histone deacetylase inhibition as part of its DNA damage response.Valproate activates bovine leukemia virus gene expression, triggers apoptosis, and induces leukemia/lymphoma regression in vivo.Clinical potential of novel therapeutic targets in breast cancer: CDK4/6, Src, JAK/STAT, PARP, HDAC, and PI3K/AKT/mTOR pathways.Synergistic epigenetic reactivation of estrogen receptor-α (ERα) by combined green tea polyphenol and histone deacetylase inhibitor in ERα-negative breast cancer cellsBioactive dietary supplements reactivate ER expression in ER-negative breast cancer cells by active chromatin modificationsManipulating protein acetylation in breast cancer: a promising approach in combination with hormonal therapies?Histone deacetylase (HDAC) inhibitors in recent clinical trials for cancer therapy.Reactivation of estrogen receptor α by vorinostat sensitizes mesenchymal-like triple-negative breast cancer to aminoflavone, a ligand of the aryl hydrocarbon receptor.Protein kinase D1 regulates ERα-positive breast cancer cell growth response to 17β-estradiol and contributes to poor prognosis in patientsA phase II study of the histone deacetylase inhibitor vorinostat combined with tamoxifen for the treatment of patients with hormone therapy-resistant breast cancerIdentification of 53 compounds that block Ebola virus-like particle entry via a repurposing screen of approved drugs.Combined histone deacetylase inhibition and tamoxifen induces apoptosis in tamoxifen-resistant breast cancer models, by reversing Bcl-2 overexpressionInhibition of breast cancer progression by a novel histone deacetylase inhibitor, LW479, by down-regulating EGFR expression.Histone deacetylase inhibitors and cancer therapy.ERalpha and ERbeta expression and transcriptional activity are differentially regulated by HDAC inhibitors.HDAC 1 and 6 modulate cell invasion and migration in clear cell renal cell carcinoma.A phase II trial of vorinostat (suberoylanilide hydroxamic acid) in metastatic breast cancer: a California Cancer Consortium studyThe phosphorylated prodrug FTY720 is a histone deacetylase inhibitor that reactivates ERα expression and enhances hormonal therapy for breast cancer.Epigenetic reactivation of estrogen receptor-α (ERα) by genistein enhances hormonal therapy sensitivity in ERα-negative breast cancer.Tamoxifen Action in ER-Negative Breast Cancer.Incorporation of histone deacetylase inhibition into the structure of a nuclear receptor agonist.Epigenetic targeting in breast cancer: therapeutic impact and future direction.Synergistic effects of combined treatment with histone deacetylase inhibitor suberoylanilide hydroxamic acid and TRAIL on human breast cancer cells.Maternal regulation of estrogen receptor alpha methylationRETRACTED: Wnt-5a signaling restores tamoxifen sensitivity in estrogen receptor-negative breast cancer cells.Will histone deacetylase inhibitors require combination with other agents to fulfil their therapeutic potential?Epigenetic modifications of the Estrogen receptor beta gene in epithelial ovarian cancer cellsAberrant promoter CpG methylation and its translational applications in breast cancer.The silent estrogen receptor--can we make it speak?Cancer epigenetics: a perspective on the role of DNA methylation in acquired endocrine resistance.New clinical developments in histone deacetylase inhibitors for epigenetic therapy of cancer.Activation of ERα signaling differentially modulates IFN-γ induced HLA-class II expression in breast cancer cells.A chimeric SERM-histone deacetylase inhibitor approach to breast cancer therapy.Modulation of gene expression in ovarian cancer by active and repressive histone marks.
P2860
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P2860
The histone deacetylase inhibitor trichostatin A sensitizes estrogen receptor alpha-negative breast cancer cells to tamoxifen.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
2004年论文
@zh
2004年论文
@zh-cn
name
The histone deacetylase inhibi ...... ast cancer cells to tamoxifen.
@en
type
label
The histone deacetylase inhibi ...... ast cancer cells to tamoxifen.
@en
prefLabel
The histone deacetylase inhibi ...... ast cancer cells to tamoxifen.
@en
P2093
P2860
P356
P1433
P1476
The histone deacetylase inhibi ...... ast cancer cells to tamoxifen.
@en
P2093
Eun Ryoung Jang
Eun Sook Lee
Gajin Jeong
Jong-Soo Lee
Soo-Jeong Lim
Tae-You Kim
Yung-Jue Bang
P2860
P2888
P304
P356
10.1038/SJ.ONC.1207315
P407
P577
2004-03-01T00:00:00Z
P5875
P6179
1026102020