| Literature DB >> 24423654 |
P H Yang1, L Zhang, Y J Zhang, J Zhang, W F Xu.
Abstract
Acetylation and deacetylation of histones are important in regulating gene expression and play a key role in modification of gene transcription. Specific HDACs isoforms can be regarded as a target for cancer therapy avoiding side-effects, HDAC6 with a unique physiological function and structure has become a hot issue recently. The unique isoform HDAC6 is involved in tumorigenesis, development and metastasis through tubulin, HSP90, invasin and ubiquitin-protein. Here we review the structure elements, biological function, and recent selective inhibitors of HDAC6, and study the structure-activity and structure-selectivity relationship.Entities:
Mesh:
Substances:
Year: 2013 PMID: 24423654 DOI: 10.5582/ddt.2013.v7.6.233
Source DB: PubMed Journal: Drug Discov Ther ISSN: 1881-7831