» Articles » PMID: 16397526

Histone Deacetylase Inhibitors and the Promise of Epigenetic (and More) Treatments for Cancer

Overview
Journal Nat Rev Cancer
Specialty Oncology
Date 2006 Jan 7
PMID 16397526
Citations 834
Authors
Affiliations
Soon will be listed here.
Abstract

Histone deacetylases (HDACs) are considered to be among the most promising targets in drug development for cancer therapy, and first-generation histone deacetylase inhibitors (HDACi) are currently being tested in phase I/II clinical trials. A wide-ranging knowledge of the role of HDACs in tumorigenesis, and of the action of HDACi, has been achieved. However, several basic aspects are not yet fully understood. Investigating these aspects in the context of what we now understand about HDACi action both in vitro and in vivo will further improve the design of optimized clinical protocols.

Citing Articles

CPSF6-RARγ interacts with histone deacetylase 3 to promote myeloid transformation in RARG-fusion acute myeloid leukemia.

Liu T, Wang T, Qi L, Liu Y, Shan M, Wang F Nat Commun. 2025; 16(1):616.

PMID: 39805830 PMC: 11729889. DOI: 10.1038/s41467-024-54860-4.


A novel histone acetylation-associated gene signature with prognostic value in Ewing sarcoma.

Wu A, Liu F, Zhou L, Jiang R, Yu S, Zhou Z Discov Oncol. 2024; 15(1):848.

PMID: 39738986 PMC: 11685356. DOI: 10.1007/s12672-024-01689-4.


Butyrate as a Potential Modulator in Gynecological Disease Progression.

Kim N, Yang C Nutrients. 2024; 16(23).

PMID: 39683590 PMC: 11644728. DOI: 10.3390/nu16234196.


Canonical androgen response element motifs are tumor suppressive regulatory elements in the prostate.

Chen X, Augello M, Liu D, Lin K, Hakansson A, Sjostrom M Nat Commun. 2024; 15(1):10675.

PMID: 39672812 PMC: 11645413. DOI: 10.1038/s41467-024-53734-z.


TRIM21-mediated ubiquitination and phosphorylation of ERK1/2 promotes cell proliferation and drug resistance in pituitary adenomas.

Liu Y, Liu F, Li C, Zhang T, Han T, Dai Y Neuro Oncol. 2024; 27(3):727-742.

PMID: 39533840 PMC: 11889717. DOI: 10.1093/neuonc/noae241.