Phase 1 study of the histone deacetylase inhibitor vorinostat (suberoylanilide hydroxamic acid [SAHA]) in patients with advanced leukemias and myelodysplastic …
G Garcia-Manero, H Yang… - Blood, The Journal …, 2008 - ashpublications.org
Vorinostat (suberoylanilide hydroxamic acid, SAHA) is a histone deacetylase inhibitor active
clinically in cutaneous T-cell lymphoma and preclinically in leukemia. A phase 1 study was …
clinically in cutaneous T-cell lymphoma and preclinically in leukemia. A phase 1 study was …
Targeting epigenetic mechanisms: potential of natural products in cancer chemoprevention
AT Hauser, M Jung - Planta medica, 2008 - thieme-connect.com
The term epigenetics is defined as heritable changes in gene expression patterns that occur
without changes in DNA sequence. Epigenetic changes according to this definition are …
without changes in DNA sequence. Epigenetic changes according to this definition are …
Expression-based screening identifies the combination of histone deacetylase inhibitors and retinoids for neuroblastoma differentiation
The discovery of new small molecules and their testing in rational combination poses an
ongoing problem for rare diseases, in particular, for pediatric cancers such as …
ongoing problem for rare diseases, in particular, for pediatric cancers such as …
Complex molecular mechanisms cooperate to mediate histone deacetylase inhibitors anti-tumour activity in neuroblastoma cells
A Mühlethaler-Mottet, R Meier, M Flahaut, KB Bourloud… - Molecular cancer, 2008 - Springer
Abstract Background Histone deacetylase inhibitors (HDACi) are a new class of promising
anti-tumour agent inhibiting cell proliferation and survival in tumour cells with very low …
anti-tumour agent inhibiting cell proliferation and survival in tumour cells with very low …
[HTML][HTML] Gastric cancer cell lines induced by trichostatin A
XM Zou, YL Li, H Wang, W Cui, XL Li… - World journal of …, 2008 - ncbi.nlm.nih.gov
AIM: To explore the effect of trichostatin A (TSA) on apoptosis and acetylated histone H3
levels in gastric cancer cell lines BGC-823 and SGC-7901. METHODS: The effect of TSA on …
levels in gastric cancer cell lines BGC-823 and SGC-7901. METHODS: The effect of TSA on …
Norsolorinic Acid from Aspergillus nidulans Inhibits the Proliferation of Human Breast Adenocarcinoma MCF‐7 Cells via Fas‐Mediated Pathway
Norsolorinic acid, isolated from the Aspergillus nidulans, was investigated for its
antiproliferative activity in human breast adenocarcinoma MCF‐7 cells. To identity the …
antiproliferative activity in human breast adenocarcinoma MCF‐7 cells. To identity the …
Carbamic acid compounds comprising a sulfonamide linkage as HDAC inhibitors
I Kalvinsh, E Loza, V Gailite - US Patent 7,407,988, 2008 - Google Patents
This invention pertains to certain active carbamic acid com pounds which inhibit HDAC
activity and which have the following formula:(1) A is an aryl group; Q'is a covalent bond or …
activity and which have the following formula:(1) A is an aryl group; Q'is a covalent bond or …
Der Einfluss von alpha-Liponsäure und weiteren HDAC-Inhibitoren auf Tumorwachstum und Angiogenese in der Pankreaskarzinomzelllinie MIA-PaCa-2
B Auer - 2008 - jlupub.ub.uni-giessen.de
Angiogenese ist die wichtigste Voraussetzung für das Wachstum und die
Metastasierungeines Tumors, da Sauerstoff und Nährstoffe für das Tumorgewebe …
Metastasierungeines Tumors, da Sauerstoff und Nährstoffe für das Tumorgewebe …
The mode of action of HC-toxin, a disease determinant of the maize pathogen Cochliobolus carbonum race 1
HA Young - 2008 - search.proquest.com
Plants are continuously bombarded by an array of potential pathogenic invaders and,
therefore, must enlist an equally diverse set of defense response mechanisms to protect …
therefore, must enlist an equally diverse set of defense response mechanisms to protect …
Epigenetic Drugs: Histone Deacetylase Inhibitors
M Peart, RW Johnstone - Epigenetics in Biology and Medicine, 2008 - taylorfrancis.com
Histone deacetylase inhibitors (HDACi) represent a novel class of anticancer compounds
that inhibit tumor cell growth and/or survival by inducing cell cycle arrest at the G1 or G2/M …
that inhibit tumor cell growth and/or survival by inducing cell cycle arrest at the G1 or G2/M …