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Thirty Years of HDAC Inhibitors: 2020 Insight and Hindsight
Journal of Medicinal Chemistry · 2020 · Vol. 63(21) · pp. 12460–12484
Terence C. S. Ho(University of East Anglia)Alex H. Y. Chan(University of East Anglia)A. Ganesan✉(University of East Anglia)
Abstract
It is now 30 years since the first report of a potent zinc-dependent histone deacetylase (HDAC) inhibitor appeared. Since then, five HDAC inhibitors have received regulatory approval for cancer chemotherapy while many others are in clinical development for oncology as well as other therapeutic indications. This Perspective reviews the biological and medicinal chemistry advances over the past 3 decades with an emphasis on the design of selective inhibitors that discriminate between the 11 human HDAC isoforms.
Histone Deacetylase Inhibitors ResearchProtein Degradation and InhibitorsPeptidase Inhibition and AnalysisHistone deacetylaseHindsight biasChemistryCancer chemotherapyPharmacologyHistone deacetylase inhibitorHistoneCancerCancer researchInternal medicine
MeSH terms
AnilidesBiological ProductsClinical Trials as TopicHistone DeacetylasesHumansHydroxamic AcidsIsoenzymesLymphomaSulfhydryl CompoundsHistone Deacetylase Inhibitors
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Cited by
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British Journal of Clinical Pharmacology · 2021 · 401 citations
References
A novel histone deacetylase 8 (HDAC8)-specific inhibitor PCI-34051 induces apoptosis in T-cell lymphomas
Leukemia · 2008 · 439 citations
Histone Deacetylase Inhibitors as Anticancer Drugs
International Journal of Molecular Sciences · 2017 · 1,159 citations
Combination Therapy With Histone Deacetylase Inhibitors (HDACi) for the Treatment of Cancer: Achieving the Full Therapeutic Potential of HDACi
Frontiers in Oncology · 2018 · 652 citations
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