Cited by 138Alzheimer's disease research and treatmentsDementia and Cognitive Impairment ResearchNeuroinflammation and Neurodegeneration Mechanisms

Comment on “ApoE-directed therapeutics rapidly clear β-amyloid and reverse deficits in AD mouse models.”

Open access
Price, Ashleigh R., Xu, Guilian, Siemienski, Zoe B., Smithson, Lisa A., Borchelt, David R., Golde, Todd E., Felsenstein, Kevin M.·2013·Science

Abstract

Cramer et al . (Reports, 23 March 2012, p. 1503; published online 9 February 2012) demonstrates short-term bexarotene treatment clearing preexisting β-amyloid deposits from the brains of APP/PS1ΔE9 mice with low amyloid burden, providing a rationale for repurposing this anticancer agent as an Alzheimer’s disease (AD) therapeutic. Using a nearly identical treatment regimen, we were unable to detect any evidence of drug efficacy despite demonstration of target engagement.

Integrity signals

Registry

Crossref · 10.1126/science.1234089

Cites

4 of 4 references verified0 citation errors · 0 not checkable

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Authors
Price, A. R., Xu, G., Siemienski, Z. B., Smithson, L. A., Borchelt, D. R., Golde, T. E., & Felsenstein, K. M.
Affiliations
University of Florida (US)
Corresponding author
  • Price, Ashleigh R.
  • Xu, Guilian
  • Felsenstein, Kevin M.
Venue
Science
Published
2013-05-24
Volume
340
Issue
6135
Pages
924-924
ISSN
  • 0036-8075 (ISSN-L)
  • 1095-9203
OpenAlex
W1972229580
Cited by
138
References
4
Citations by year
2024: 1 · 2023: 4 · 2022: 3 · 2021: 6 · 2020: 8 · 2019: 9 · 2018: 7 · 2017: 8 · 2016: 22 · 2015: 27 · 2014: 30 · 2013: 13
Type
journal article
Language
en
Open access
Locations
  • Science (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
  • Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
  • Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
Keywords
bexarotene, apolipoprotein E, amyloid-beta clearance, Alzheimer's disease, drug repurposing, target engagement, drug efficacy, amyloid plaques
MeSH terms
Alzheimer Disease, Animals, Apolipoproteins E, Brain, Male, Tetrahydronaphthalenes, Amyloid beta-Peptides

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