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A Need for Refined Senescence Biomarkers and Measures of Senolytics in the Brain
Journal of Alzheimer s Disease · 2024 · ▲ 5 citations
Abstract
Cellular senescence(definition) contributes to Alzheimer's disease (AD) pathogenesis. Treatments that remove senescent cells, senolytics(definition), improve brain outcomes in AD mice with amyloid-β or tau deposition. 3xTgAD mice develop both AD neuropathologies; however, Ng et al. report low p16INK4a-associated senescence in the brain. Senolytic treatment by genetic removal; dasatinib with quercetin (D+Q), which enter the brain; and ABT-263 with limited brain penetrance all reduced AD neuropathology. Refined measures of senescence and brain exposure would help clarify the benefits of senolytics despite low p16INK4a-associated senescence and potential limited brain penetrance.
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- 10.3233/jad-231462
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- 2026-06-15 MST
Cite this
APA
Orr, M.E. (2024). A Need for Refined Senescence Biomarkers and Measures of Senolytics in the Brain. <em>Journal of Alzheimer s Disease</em>. https://doi.org/10.3233/jad-231462
Vancouver
Orr ME. A Need for Refined Senescence Biomarkers and Measures of Senolytics in the Brain. Journal of Alzheimer s Disease. 2024. doi:10.3233/jad-231462.
BibTeX
@unpublished{miranda2024ANeedf,
title = {A Need for Refined Senescence Biomarkers and Measures of Senolytics in the Brain},
author = {Miranda E. Orr},
journal = {Journal of Alzheimer s Disease},
year = {2024},
doi = {10.3233/jad-231462},
}
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