Histone deacetylase inhibitor LAQ824 down-regulates Her-2 and sensitizes human breast cancer cells to trastuzumab, taxotere, gemcitabine, and epothilone B

L Fuino, P Bali, S Wittmann, S Donapaty, F Guo… - Molecular cancer …, 2003 - AACR
Histone deacetylase inhibitors induce hyperacetylation of the amino-terminal lysine residues
of the core nucleosomal histones, which results in chromatin remodeling and altered gene …

Activity of suberoylanilide hydroxamic Acid against human breast cancer cells with amplification of her-2

P Bali, M Pranpat, R Swaby, W Fiskus… - Clinical cancer …, 2005 - AACR
Purpose: We determined the effects of suberoylanilide hydroxamic acid (SAHA), a histone
deacetylase inhibitor, on hsp90 and its client proteins Her-2, AKT, and c-Raf, as well as …

Histone deacetylase (HDAC) inhibitor activation of p21WAF1 involves changes in promoter-associated proteins, including HDAC1

CY Gui, L Ngo, WS Xu, VM Richon… - Proceedings of the …, 2004 - National Acad Sciences
Histone deacetylase (HDAC) inhibitors (HDACi) cause cancer cell growth arrest and/or
apoptosis in vivo and in vitro. The HDACi suberoylanilide hydroxamic acid (SAHA) is in …

A novel HSP90 inhibitor targeting the C-terminal domain attenuates trastuzumab resistance in HER2-positive breast cancer

JM Park, YJ Kim, S Park, M Park, L Farrand… - Molecular Cancer, 2020 - Springer
Trastuzumab resistance in HER2-positive breast cancer is associated with a poorer
prognosis. HSP90 is thought to play a major role in such resistance, but N-terminal inhibitors …

The histone deacetylase inhibitor MS-275 promotes differentiation or apoptosis in human leukemia cells through a process regulated by generation of reactive oxygen …

RR Rosato, JA Almenara, S Grant - Cancer research, 2003 - AACR
Abstract Effects of the histone deacetylase (HDAC) inhibitor MS-275 have been examined in
human leukemia and lymphoma cells (U937, HL-60, K562, and Jurkat) as well as in primary …

A new synthetic histone deacetylase inhibitor, MHY2256, induces apoptosis and autophagy cell death in endometrial cancer cells via p53 acetylation

U De, JY Son, R Sachan, YJ Park, D Kang… - International Journal of …, 2018 - mdpi.com
We previously discovered a novel sirtuin (SIRT) inhibitor, MHY2256, that exerts anticancer
activity through p53 acetylation in MCF-7 human breast cancer cells. We investigated the …

Histone deacetylase inhibitors all induce p21 but differentially cause tubulin acetylation, mitotic arrest, and cytotoxicity

MV Blagosklonny, R Robey, DL Sackett, L Du… - Molecular cancer …, 2002 - AACR
By preventing deacetylation of histones, histone deacetylase inhibitors (HDIs)
transcriptionally induce p21. Here we show that the HDIs sodium butyrate (Bu), trichostatin A …

Inhibition of HSP90 with AUY922 induces synergy in HER2-amplified trastuzumab-resistant breast and gastric cancer

ZA Wainberg, A Anghel, AM Rogers, AJ Desai… - Molecular cancer …, 2013 - AACR
HSP90 enables the activation of many client proteins of which the most clinically validated is
HER2. NVP-AUY922, a potent HSP90 inhibitor, is currently in phase II clinical trials. To …

Modulation of p53, ErbB1, ErbB2, and Raf-1 expression in lung cancer cells by depsipeptide FR901228

X Yu, ZS Guo, MG Marcu, L Neckers… - Journal of the …, 2002 - academic.oup.com
Abstract Background: Histone deacetylases (HDACs) modulate chromatin structure by
regulating acetylation of core histone proteins. HDAC inhibitors, such as depsipeptide …

Histone deacetylase inhibitor selectively induces p21WAF1 expression and gene-associated histone acetylation

VM Richon, TW Sandhoff… - Proceedings of the …, 2000 - National Acad Sciences
Histone deacetylases (HDACs) catalyze the removal of acetyl groups on the amino-terminal
lysine residues of core nucleosomal histones. This activity is associated generally with …