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Updated: Aug 9, 2025

Characterizing Histone Post-translational Modification Alterations in Yeast Neurodegenerative Proteinopathy Models
Published on: March 24, 2019
Histone Modifications in Alzheimer's Disease
Dalileia Aparecida Santana1, Marilia de Arruda Cardoso Smith1, Elizabeth Suchi Chen1
1Department of Morphology & Genetics, Universidade Federal de São Paulo (UNIFESP), São Paulo 04023-062, SP, Brazil.
Epigenetic histone modifications, like acetylation and methylation, are implicated in late-onset Alzheimer's disease (LOAD). This review explores their role and potential therapeutic targets, including histone deacetylase inhibitors for AD treatment.
Area of Science:
- Neuroscience
- Genetics
- Epigenetics
Background:
- Late-onset Alzheimer's disease (LOAD) involves genetic and environmental factors, with epigenetics playing a potential role.
- Histone modifications are key epigenetic mechanisms contributing to LOAD's pathology, but their specific roles in disease onset and progression are not fully understood.
Purpose of the Study:
- To review the primary histone modifications (acetylation, methylation, phosphorylation) and their functions.
- To examine how these histone modifications change during aging and in Alzheimer's disease (AD).
- To discuss epigenetic drugs, specifically histone deacetylase (HDAC) inhibitors, being investigated for AD treatment.
Main Methods:
- Literature review of histone modifications in aging and Alzheimer's disease.
- Analysis of functional roles of histone acetylation, methylation, and phosphorylation.
- Overview of current epigenetic drug therapies for AD.
Main Results:
- Histone modifications are altered during aging and are implicated in Alzheimer's disease pathogenesis.
- Specific histone modifications influence the molecular mechanisms underlying AD.
- Histone deacetylase inhibitors show promise as a therapeutic strategy for AD.
Conclusions:
- Epigenetic histone modifications are crucial in the development and progression of Alzheimer's disease.
- Targeting histone modifications with drugs like HDAC inhibitors offers a potential therapeutic avenue for AD treatment.
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