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Class I and II histone deacetylase expression is not altered in human amyotrophic lateral sclerosis: Neuropathological and positron emission tomography molecular neuroimaging evidence
Author(s) -
Dios Amanda M.,
Babu Suma,
Granucci Eric J.,
Mueller Kaly A.,
Mills Alexandra N.,
Alshikho Mohamad J.,
Zürcher Nicole R.,
Cernasov Paul,
Gilbert Tonya M.,
Glass Jonathan D.,
Berry James D.,
Atassi Nazem,
Hooker Jacob M.,
SadriVakili Ghazaleh
Publication year - 2019
Publication title -
muscle and nerve
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.025
H-Index - 145
eISSN - 1097-4598
pISSN - 0148-639X
DOI - 10.1002/mus.26620
Subject(s) - amyotrophic lateral sclerosis , positron emission tomography , blot , histone deacetylase , medicine , gene isoform , neuroimaging , trichostatin a , pathology , histone deacetylase 5 , histone , cancer research , microbiology and biotechnology , biology , neuroscience , disease , nuclear medicine , biochemistry , gene
There is an unmet need for mechanism‐based biomarkers and effective disease modifying treatments in amyotrophic lateral sclerosis (ALS). Previous findings have provided evidence that histone deacetylases (HDAC) are altered in ALS, providing a rationale for testing HDAC inhibitors as a therapeutic option. Methods We measured class I and II HDAC protein and transcript levels together with acetylation levels of downstream substrates by using Western blotting in postmortem tissue of ALS and controls. [ 11 C]Martinostat, a novel HDAC positron emission tomography ligand, was also used to assess in vivo brain HDAC alterations in patients with ALS and healthy controls (HC). Results There was no significant difference in HDAC levels between patients with ALS and controls as measured by Western blotting and reverse‐transcription quantitative polymerase chain reaction. Similarly, no differences were detected in [ 11 C]Martinostat–positron emission tomography uptake in ALS participants compared with HCs. Discussion These findings provide evidence that alterations in HDAC isoforms are not a dominant pathological feature at the bulk tissue level in ALS.