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. Author manuscript; available in PMC: 2014 Oct 1.
Published in final edited form as: Nucl Med Biol. 2013 Jul 29;40(7):912–918. doi: 10.1016/j.nucmedbio.2013.06.007

Table 1.

Publications on BA, PBA, VA related to HDAC in human diseases.

Disease/Process Relevance BA PBA VPA
Anemias HDAC inhibition stimulates fetal hemoglobin (HbF) production (particularly relevant to sickle cell anemia). h [5, 8]; r [11] h [9] h [6, 10]
Cancer HDAC inhibitors increase the sensitivity of many types of cancer to traditional chemotherapeutics. m [12–14] h [15, 16]; h [17]
immune modulation HDAC inhibition appears to exhibit anti-inflammatory properties, reducing the activation of the NF-κB cascade and inhibiting the production of inflammatory cytokines. m [7, 12] m [18] m [19]
neurological/psyc hiatric HDAC inhibitors have been tested for psychiatric illness treatment; they exhibit neuroprotective properties. HDAC inhibition has reversed symptoms in animal models of Alzheimer’s, ALS, and muscle atrophy. HDAC inhibitors have been shown to reduce the severity of neuropathic pain and they have also been shown to enhance memory and learning in laboratory animals. m [20]
m [21]
h [22, 23]; r [24]; m [25] m [26]; h[27, 28]
Others Inflammatory bowel disease (BA), diabetes (PBA), HIV (VPA) h [29, 30]; h [31]; h [2]

Abbreviations: h (human); r (rat); m (mouse); BA (butyric acid); PBA (phenylbutyric acid); VPA (valproic acid).