Evidence map›Paper›PMID 29579087›Full record

ArticlePloS one2018

Class I HDAC inhibition is a novel pathway for regulating astrocytic apoE secretion.

Erica Dresselhaus, James M Duerr, Fabien Vincent, Emily K Sylvain, Mercedes Beyna, Lorraine F Lanyon, Erik LaChapelle, Martin Pettersson, Kelly R Bales, Gayathri Ramaswamy

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.8field-weighted citation impact, top 7% 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

13 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Targeting Apolipoprotein E for Alzheimer's Disease: An Industry Perspective.International journal of molecular sciences · 2019
    Review
  13. 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

10 authors at 1 institution in 1 country.

Erica DresselhausInternal Medicine Research Unit, Pfizer, Cambridge, Massachusetts, United States of America.
James M DuerrInternal Medicine Research Unit, Pfizer, Cambridge, Massachusetts, United States of America.
Fabien VincentHit Discovery and Lead Profiling, Pfizer, Groton, Connecticut, United States of America.
Emily K SylvainInternal Medicine Research Unit, Pfizer, Cambridge, Massachusetts, United States of America.
Mercedes BeynaInternal Medicine Research Unit, Pfizer, Cambridge, Massachusetts, United States of America.
Lorraine F LanyonHit Discovery and Lead Profiling, Pfizer, Groton, Connecticut, United States of America.
Erik LaChapelleMedicinal Chemistry, Pfizer, Groton, Connecticut, United States of America.
Martin PetterssonMedicinal Chemistry, Pfizer, Cambridge, Massachusetts, United States of America.
Kelly R BalesInternal Medicine Research Unit, Pfizer, Cambridge, Massachusetts, United States of America.
Gayathri RamaswamyInternal Medicine Research Unit, Pfizer, Cambridge, Massachusetts, United States of America.ORCID 0000-0001-7658-408X
Pfizer (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite the important role of apolipoprotein E (apoE) secretion from astrocytes in brain lipid metabolism and the strong association of apoE4, one of the human apoE isoforms, with sporadic and late onset forms of Alzheimer's disease (AD) little is known about the regulation of astrocytic apoE. Utilizing annotated chemical libraries and a phenotypic screening strategy that measured apoE secretion from a human astrocytoma cell line, inhibition of pan class I histone deacetylases (HDACs) was identified as a mechanism to increase apoE secretion. Knocking down select HDAC family members alone or in combination revealed that inhibition of the class I HDAC family was responsible for enhancing apoE secretion. Knocking down LXRα and LXRβ genes revealed that the increase in astrocytic apoE in response to HDAC inhibition occurred via an LXR-independent pathway. Collectively, these data suggest that pan class I HDAC inhibition is a novel pathway for regulating astrocytic apoE secretion.

Indexed as

Apolipoproteins EAstrocytesATP Binding Cassette Transporter 1BenzenesulfonamidesCells, CulturedEnzyme-Linked Immunosorbent AssayFluorocarbonsGenotypeHistone Deacetylase InhibitorsHistone DeacetylasesHumansHydrocarbons, FluorinatedLiver X ReceptorsProtein BindingProtein IsoformsRNA InterferenceApolipoproteins EATP Binding Cassette Transporter 1BenzenesulfonamidesFluorocarbonsHistone Deacetylase InhibitorsHistone DeacetylasesHydrocarbons, FluorinatedLiver X ReceptorsProtein IsoformsRNA, MessengerRNA, Small InterferingSmall Molecule LibrariesSulfonamidesT0901317

Identifiers

PMID29579087
PMCPMC5868809
OpenAlexW2794406984

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.