Evidence map›Paper›PMID 28450396›Full record

ArticleThe Journal of biological chemistry2017

Heat-shock protein 90 (Hsp90) promotes opioid-induced anti-nociception by an ERK mitogen-activated protein kinase (MAPK) mechanism in mouse brain.

Wei Lei, Nathan Mullen, Sarah McCarthy, Courtney Brann, Philomena Richard, James Cormier, Katie Edwards, Edward J Bilsky, John M Streicher

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
4.2field-weighted citation impact, top 5% 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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 59 citations in OpenAlex.

  1. Pooled it
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  15. The heat shock response and small molecule regulators.European journal of medicinal chemistry · 2021
    Review
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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

9 authors at 3 institutions in 1 country.

Wei LeiFrom the Department of Pharmacology, College of Medicine, University of Arizona, Tucson, Arizona 85724.
Nathan Mullenthe Department of Biomedical Sciences, College of Osteopathic Medicine, University of New England, Biddeford, Maine 04005, and.
Sarah McCarthythe Department of Biomedical Sciences, College of Osteopathic Medicine, University of New England, Biddeford, Maine 04005, and.
Courtney Brannthe Department of Biomedical Sciences, College of Osteopathic Medicine, University of New England, Biddeford, Maine 04005, and.
Philomena Richardthe Department of Biomedical Sciences, College of Osteopathic Medicine, University of New England, Biddeford, Maine 04005, and.
James Cormierthe Department of Biomedical Sciences, College of Osteopathic Medicine, University of New England, Biddeford, Maine 04005, and.
Katie Edwardsthe Department of Biomedical Sciences, College of Osteopathic Medicine, University of New England, Biddeford, Maine 04005, and.
Edward J Bilskythe Department of Biomedical Sciences, College of Osteopathic Medicine, University of New England, Biddeford, Maine 04005, and.
John M StreicherFrom the Department of Pharmacology, College of Medicine, University of Arizona, Tucson, Arizona 85724, jstreicher@email.arizona.edu.ORCID 0000-0002-4173-7362
University of New England · USUniversity of Arizona · USPacific Northwest University of Health Sciences · US

Funding

Tissue resident macrophages in sensory ganglia: function and impact on nociceptionP20GM103643 · NIGMS · UNIVERSITY OF NEW ENGLAND · PI MENG, IAN D · 2012 to 2021
$20.9M
NIGMS NIH HHS P20 GM103643
6 · The paper itself

Abstract

Recent advances in developing opioid treatments for pain with reduced side effects have focused on the signaling cascades of the μ-opioid receptor (MOR). However, few such signaling targets have been identified for exploitation. To address this need, we explored the role of heat-shock protein 90 (Hsp90) in opioid-induced MOR signaling and pain, which has only been studied in four previous articles. First, in four cell models of MOR signaling, we found that Hsp90 inhibition for 24 h with the inhibitor 17-

Indexed as

Analgesics, OpioidAnimalsBenzoquinonesBrain StemCHO CellsCricetinaeCricetulusExtracellular Signal-Regulated MAP KinasesHEK293 CellsHSP90 Heat-Shock ProteinsHumansLactams, MacrocyclicMaleMAP Kinase Signaling SystemMiceNeuralgiaAnalgesics, OpioidBenzoquinonesExtracellular Signal-Regulated MAP KinasesHSP90 Heat-Shock ProteinsLactams, Macrocyclictanespimycin17-AAGanti-nociceptionbrainextracellular-signal-regulated kinase (ERK)heat-shock protein 90 (Hsp90)opiate opioidpainμ-opioid receptor

Identifiers

PMID28450396
PMCPMC5481554
OpenAlexW2608001712

What OpenQuestion holds

Textmetadata
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.