scispace - formally typeset
Journal ArticleDOI

Histone deacetylase inhibitors.

Claude Monneret
- 01 Jan 2005 - 
- Vol. 40, Iss: 1, pp 1-13
TLDR
Design of a second generation ofHDACs was based upon data affording potent HDACs such as LAQ824 and PDX101 currently under phase I clinical trials, and two of them, MS-275 and CI-994, have reached phase II and I clinical Trials, respectively.
About
This article is published in European Journal of Medicinal Chemistry.The article was published on 2005-01-01. It has received 819 citations till now. The article focuses on the topics: Histone deacetylase & Phenylbutyrate.

read more

Citations
More filters
Journal ArticleDOI

A Convenient Synthesis of the New Histone Deacetylase Inhibitor Scriptaid

TL;DR: A recent in vitro study revealed that scriptaid provoked growth inhibition, cell cycle arrest and apoptosis in human endometrial cancer and ovarian cancer cells, confirming the effect of scriptaid as HDAC inhibitor.
Journal ArticleDOI

Intrabody-mediated diverting of HP1β to the cytoplasm induces co-aggregation of H3–H4 histones and lamin-B receptor

TL;DR: It is found that the anti-HP1β intrabody sequesters HP1β into cytoplasmic aggregates, inhibiting its traffic to the nucleus, providing new insights into the mode of action of cytopLasmic-targeted intrabodies and the interaction between HP1 β and its binding partners involved in peripheral heterochromatin organisation.
BookDOI

Cell Signaling & Molecular Targets in Cancer

TL;DR: Book of cell signaling molecular targets in cancer, as an amazing reference becomes what you need to get, as a source that may involve the facts, opinion, literature, religion, and many others are the great friends to join with.
Journal ArticleDOI

The Effect of Sodium Butyrate on Adventitious Shoot Formation Varies among the Plant Species and the Explant Types.

TL;DR: The effect of NaB on adventitious shoot formation and expression of CYCD3-1 and WUS genes depended on the plant species and whether the effects were tested on explants or protoplast-derived calli.
Journal ArticleDOI

FK228 Analogues Induce Fetal Hemoglobin in Human Erythroid Progenitors

TL;DR: Investigation of the ability of FK228 analogues to induce HbF using a novel KU812 dual-luciferase reporter system supports lead compounds as potential therapeutic agents for further development in the treatment of SCD.
References
More filters
Journal ArticleDOI

Crystal structure of the nucleosome core particle at 2.8 Å resolution

TL;DR: The X-ray crystal structure of the nucleosome core particle of chromatin shows in atomic detail how the histone protein octamer is assembled and how 146 base pairs of DNA are organized into a superhelix around it.
Journal ArticleDOI

hSIR2SIRT1 Functions as an NAD-Dependent p53 Deacetylase

TL;DR: It is proposed that hSir2, the human homolog of the S. cerevisiae Sir2 protein known to be involved in cell aging and in the response to DNA damage, binds and deacetylates the p53 protein with a specificity for its C-terminal Lys382 residue.
Journal ArticleDOI

Negative Control of p53 by Sir2α Promotes Cell Survival under Stress

TL;DR: It is shown that mammalian Sir2alpha physically interacts with p53 and attenuates p53-mediated functions, and Nicotinamide inhibits an NAD-dependent p53 deacetylation induced by Sir2 alpha, and also enhances the p53 acetylation levels in vivo.
Journal ArticleDOI

Potent and specific inhibition of mammalian histone deacetylase both in vivo and in vitro by trichostatin A.

TL;DR: Results clearly indicate that TSA is a potent and specific inhibitor of the histone deacetylase and that the in vivo effect of TSA on cell proliferation and differentiation can be attributed to the inhibition of the enzyme.
Journal ArticleDOI

Valproic acid defines a novel class of HDAC inhibitors inducing differentiation of transformed cells

TL;DR: Valproic acid induces differentiation of carcinoma cells, transformed hematopoietic progenitor cells and leukemic blasts from acute myeloid leukemia patients, and tumor growth and metastasis formation are significantly reduced in animal experiments, suggesting that it might serve as an effective drug for cancer therapy.
Related Papers (5)