Results 1 to 10 of about 116,207 (325)

Differential effects of HDAC inhibitors in the Rho I255d mouse model for autosomal dominant retinitis pigmentosa [PDF]

open access: yesCell Death Discovery
Retinitis Pigmentosa (RP) is an inherited neurodegenerative disease which leads to loss of retinal photoreceptors and blindness. Histone deacetylases (HDAC) were previously found to be involved in photoreceptor cell death, and HDAC inhibitors have shown ...
Yu Zhu   +3 more
doaj   +2 more sources

Next-Generation HDAC Inhibitors: Advancing Zinc-Binding Group Design for Enhanced Cancer Therapy [PDF]

open access: yesCells
Histone deacetylases (HDACs) are pivotal epigenetic regulators that control gene expression, cell proliferation, and differentiation, and their dysregulation is closely associated with the onset and progression of multiple cancers.
Mohammed Hawash
doaj   +2 more sources

EFFECT OF SAHA AND C-JUN N-TERMINAL KINASE INHIBITOR ON THE INDUCIBLE MRNA EXPRESSION OF INTERLEUKIN-17 [PDF]

open access: yesJournal of IMAB, 2023
Interleukin-17 (IL-17A) is a critical cytokine for immune defence against extracellular bacterial and fungal infections. Excess production during chronic inflammation has been associated with many inflammatory and autoimmune disorders. On the other hand,
Boncho Grigorov   +4 more
doaj   +1 more source

The Effect of Quisinostat as the HDAC Inhibitor on Migration [PDF]

open access: yesMajallah-i dānishgāh-i ̒ulūm-i pizishkī-i Arāk, 2021
Background and Aim: Cancer cannot be explained only by genetic alterations but involves epigenetic processes. Modifying histones by acetylation plays a key role in epigenetic regulation of gene expression and is controlled by the balance between Histone ...
Marjan Hajimoradi Javarsiani   +2 more
doaj   +3 more sources

Evaluation of histone deacetylase inhibitory and antiproliferative activity of piperine and its derivatives [PDF]

open access: yesSongklanakarin Journal of Science and Technology (SJST), 2022
Piperine (1) was obtained from the seeds of Piper nigrum L. It could act as a pan-histone deacetylase (HDAC) inhibitor. This lead compound was structurally modified to six derivatives that exhibited improved HDAC inhibitory activity.
La-or Somsakeesit   +6 more
doaj   +1 more source

Tumor Anti-Initiation and Anti-Progression Properties of Sulphated-Extract of Colocasia esculenta

open access: yesPolish Journal of Food and Nutrition Sciences, 2021
Colocasia esculenta (Taro) is an edible tuberous plant; however, corms are its most worldwide consumed part while the corm powder is widely used in food industries. In this work, a sulphated polysaccharide extract of C.
Amira M. Gamal-Eldeen   +6 more
doaj   +1 more source

The efficacy of HDAC inhibitors in neoplasm treatment

open access: yesJournal of Education, Health and Sport, 2020
Introduction and purpose: Histone Deacetylases (HDACs) are associated with epigenetic regulation of gene expression. They are responsible of adequate action of not only histone proteins, but also crucial cell cycle proteins, such as p53, NF‐κB or alpha ...
Dominika Psiuk   +4 more
doaj   +1 more source

Exploration of Novel Mono Hydroxamic Acid Derivatives as Inhibitors for Histone Deacetylase Like Protein (HDLP) by Molecular Dynamics Studies

open access: yesIndonesian Journal of Chemistry, 2022
The acetylation modification process of histone has an essential role in the epigenetic regulation of gene expression. This process is controlled by the balance between histone deacetylases (HDAC) and histone acetyltransferases (HAT).
Gunasingham Parthiban   +4 more
doaj   +1 more source

Multitarget Anticancer Agents Based on Histone Deacetylase and Protein Kinase CK2 inhibitors

open access: yesMolecules, 2020
The design of multitarget drugs (MTDs) has become an innovative approach for the search of effective treatments in complex diseases such as cancer. In this work, we communicate our efforts in the design of multi-targeting histone deacetylase (HDAC) and ...
Regina Martínez   +9 more
doaj   +1 more source

Effect of 3-subsitution of quinolinehydroxamic acids on selectivity of histone deacetylase isoforms

open access: yesJournal of Enzyme Inhibition and Medicinal Chemistry, 2021
A series of 3-subsituted quinolinehydroxamic acids has been synthesised and evaluated for their effect on human lung cancer cell line (A549), human colorectal cancer cell line (HCT116) and HDAC isoforms 1, 2, 6, and 8.
Samir Mehndiratta   +6 more
doaj   +1 more source

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