| Literature DB >> 24318952 |
Mary E Manson McManamy1, Shweta Hakre, Eric M Verdin, David M Margolis.
Abstract
Persistence of HIV-1 in latently infected CD4(+) T-cells prevents eradication in HIV-infected treated patients. Latency is characterized by a reversible silencing of transcription of integrated HIV-1. Several molecular mechanisms have been described which contribute to latency, including the establishment and maintenance of repressive chromatin on the HIV-1 promoter. Histone deacetylation is a landmark modification associated with transcriptional repression of the HIV-1 promoter and inhibition of histone deacetylase enzymes (HDACs) reactivates latent HIV-1. Here, we review the different HDAC inhibitors that have been studied in HIV-1 latency and their therapeutic potential in reactivating latent HIV-1.Entities:
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Year: 2014 PMID: 24318952 PMCID: PMC3947511 DOI: 10.3851/IMP2551
Source DB: PubMed Journal: Antivir Chem Chemother ISSN: 0956-3202