Inhibitors of DNA Methylation and Histone Deacetylation as Epigenetically Active Drugs for Anticancer Therapy.


Journal

Current pharmaceutical design
ISSN: 1873-4286
Titre abrégé: Curr Pharm Des
Pays: United Arab Emirates
ID NLM: 9602487

Informations de publication

Date de publication:
2019
Historique:
received: 25 02 2019
accepted: 29 03 2019
pubmed: 6 4 2019
medline: 11 2 2020
entrez: 6 4 2019
Statut: ppublish

Résumé

Gene expression is regulated and tightly controlled by epigenetic mechanisms. Alterations of these mechanisms are frequently observed in various diseases, particularly, in various types of cancer. Malignant transformation is caused by the impairment of the mechanisms of cell differentiation and cell cycle control associated with epigenetic changes. Altered patterns of epigenetic modification associated with malignancies can potentially be reversed by some agents that act on the key proteins responsible for DNA/histone modification and chromatin remodelling. Examples of such substances include the inhibitors of DNA methyltransferases or histone deacetylase. During the recent years, a number of such substances have been evaluated as potential therapeutic agents against certain types of cancer in preclinical and clinical studies, and some of them have been approved for treatment of hematological cancers. Application of epidrugs for therapy of solid tumors remains, however, more challenging. In this review, we summarize the current knowledge on the most studied mechanisms of epigenetic modification and the available epigenetically active drugs.

Identifiants

pubmed: 30950345
pii: CPD-EPUB-97839
doi: 10.2174/1381612825666190405144026
doi:

Substances chimiques

Antineoplastic Agents 0
Histone Deacetylase Inhibitors 0
Histones 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

635-641

Informations de copyright

Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.

Auteurs

Veronika A Myasoedova (VA)

Laboratory of Angiopathology, Institute of General Pathology and Pathophysiology, Moscow 125315, Russian Federation.

Vasily Sukhorukov (V)

Laboratory of Angiopathology, Institute of General Pathology and Pathophysiology, Moscow 125315, Russian Federation.
Research Institute of Human Morphology, Moscow 117418, Russian Federation.

Andrey V Grechko (AV)

Federal Research and Clinical Center of Intensive Care Medicine and Rehabilitology, Moscow 109240, Russian Federation.

Dongwei Zhang (D)

Traditional Chinese Medicine School, Beijing University of Chinese Medicine, Beijing 100029, China.

Elena Romanenko (E)

Belozersky Institute of Physical and Clinical Biology, Moscow, Russian Federation.

Vawain Orekhov (V)

Laboratory of Angiopathology, Institute of General Pathology and Pathophysiology, Moscow 125315, Russian Federation.

Alexander N Orekhov (AN)

Laboratory of Angiopathology, Institute of General Pathology and Pathophysiology, Moscow 125315, Russian Federation.
Institute for Atherosclerosis Research, Skolkovo Innovative Center, Moscow 121609, Russian Federation.

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Classifications MeSH