Evidence map›Paper›PMID 32714601›Full record

ReviewNeuronal signaling2020

The class II histone deacetylases as therapeutic targets for Parkinson's disease.

Martina Mazzocchi, Louise M Collins, Aideen M Sullivan, Gerard W O'Keeffe

Open access · goldAbstract readReview
In one paragraph

Review in Neuronal signaling, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.3field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 41 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Disruption of axonal transport in neurodegeneration.The Journal of clinical investigation · 2023
    Review
  7. Review
  8. Review
  9. Article
  10. Histone Modifications in Neurological Disorders.Advances in experimental medicine and biology · 2022
    Review
  11. Review
  12. Review
  13. Review
  14. Neuronal signaling · 2021
    Article
  15. Article
  16. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Martina MazzocchiDepartment of Anatomy and Neuroscience, and Cork Neuroscience Centre, Western Gateway Building, University College Cork, Cork, Ireland.
Louise M CollinsDepartment of Anatomy and Neuroscience, and Cork Neuroscience Centre, Western Gateway Building, University College Cork, Cork, Ireland.
Aideen M SullivanDepartment of Anatomy and Neuroscience, and Cork Neuroscience Centre, Western Gateway Building, University College Cork, Cork, Ireland.ORCID 0000-0001-9692-6438
Gerard W O'KeeffeDepartment of Anatomy and Neuroscience, and Cork Neuroscience Centre, Western Gateway Building, University College Cork, Cork, Ireland.ORCID 0000-0001-5149-0933
University College Cork · IE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Parkinson's disease (PD) is a progressive neurodegenerative disorder characterised by specific motor impairments. The neuropathological hallmarks of PD include progressive degeneration of midbrain dopaminergic neurons, and loss of their axonal projections to the striatum. Additionally, there is progressive accumulation and spread of intracellular aggregates of α-synuclein. Although dopamine-replacement pharmacotherapy can treat PD symptoms in the short-term, there is a critical need for the development of disease-modifying therapies based on an understanding of the underlying disease mechanisms. One such mechanism is histone acetylation, which is a common epigenetic modification that alters gene transcription. A number of studies have described alterations in histone acetylation in the brains of PD patients. Moreover, α-synuclein accumulation has been linked to alterations in histone acetylation and pharmacological strategies aimed at modulating histone acetylation are under investigation as novel approaches to disease modification in PD. Currently, such strategies are focused predominantly on pan-inhibition of histone deacetylase (HDAC) enzymes. Inhibition of specific individual HDAC enzymes is a more targeted strategy that may allow for future clinical translation. However, the most appropriate class of HDACs that should be targeted for neuroprotection in PD is still unclear. Recent work has shed new light on the role of class-II HDACs in dopaminergic degeneration. For this reason, here we describe the regulation of histone acetylation, outline the evidence for alterations in histone acetylation in the PD brain, and focus on the roles of class II HDACs and the potential of class-II HDAC inhibition as a therapeutic approach for neuroprotection in PD.

Indexed as

dopamine neuronHDAChistone deacetylaseneuroprotectionParkinsons diseaseα-synuclein

Identifiers

PMID32714601
PMCPMC7373248
OpenAlexW3028924383

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.