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  5. Evaluation of the Therapeutic Potential of Histone Deacetylase 6 Inhibitors for Primary and Metastatic Uveal Melanoma
 
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Evaluation of the Therapeutic Potential of Histone Deacetylase 6 Inhibitors for Primary and Metastatic Uveal Melanoma

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Author(s)
Sundaramurthi, Husvinee 
Giricz, Zoltán 
Kennedy, Breandán 
Uri
http://hdl.handle.net/10197/13203
Date Issued
19 August 2022
Date Available
14T16:00:03Z October 2022
Abstract
Patients diagnosed with metastatic uveal melanoma (MUM) have a poor survival prognosis. Unfortunately for this rare disease, there is no known cure and suitable therapeutic options are limited. HDAC6 inhibitors (HDAC6i) are currently in clinical trials for other cancers and show potential beneficial effects against tumor cell survival in vitro and in vivo. In MUM cells, HDAC6i show an anti-proliferative effect in vitro and in preclinical xenograft models. The use of HDAC6 inhibitors as a treatment option for MUM should be explored further. Therefore, this review discusses (1) what is known about HDAC6i in MUM and (2) whether HDAC6 inhibitors offer a potential therapeutic option for MUM.
Sponsorship
European Commission Horizon 2020
Irish Research Council
Other Sponsorship
Breakthrough Cancer Research
National Research, Development and Innovation Office (NKFIH) of Hungary
Ministry for Innovation and Technology
National Research Development and Innovation Fund
Type of Material
Review
Publisher
MDPI
Journal
International Journal of Molecular Sciences
Volume
23
Issue
16
Start Page
1
End Page
16
Copyright (Published Version)
2022 The Authors
Keywords
  • Primary and metastati...

  • HDAC6 inhibitors

  • HDAC isozymes

  • Extracellular vesicle...

  • Combinatorial therapi...

DOI
10.3390/ijms23169378
Language
English
Status of Item
Peer reviewed
ISSN
1661-6596
This item is made available under a Creative Commons License
https://creativecommons.org/licenses/by/3.0/ie/
Owning collection
Biomolecular and Biomedical Science Research Collection
Scopus© citations
0
Acquisition Date
Mar 20, 2023
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Acquisition Date
Mar 20, 2023
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Acquisition Date
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