Evidence map›Paper›PMID 20668208›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2010

Regulation of opioid tolerance by let-7 family microRNA targeting the mu opioid receptor.

Ying He, Cheng Yang, Chelsea M Kirkmire, Zaijie Jim Wang

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 109 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
109citing papers in PubMed, 1 pooled it
5.5field-weighted citation impact, top 4% 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

109 citing papers in PubMed, 1 synthesis or guideline pooled it, 182 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Extracellular vesicle-mediated delivery of anti-miR-106b inhibits morphine-induced primary ciliogenesis in the brain.Molecular therapy : the journal of the American Society of Gene Therapy · 2023
    Article
  9. Review
  10. Evaluation of microRNA let-7b-3p expression levels in methamphetamine abuse.Revista da Associacao Medica Brasileira (1992) · 2023
    Article
  11. Extracellular Vesicles in Mental Disorders: A State-of-art Review.International journal of biological sciences · 2023
    Review
  12. Review
  13. Epigenetic Modulation of Opioid Receptors by Drugs of Abuse.International journal of molecular sciences · 2022
    Review
  14. Review
  15. Review
  16. Article
  17. Article
  18. Noncoding RNA therapeutics for substance use disorder.Advances in drug and alcohol research · 2022
    Article
  19. Article
  20. Article

49 more citing papers are in PubMed but not listed here.

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

4 authors at 1 institution in 1 country.

Ying HeDepartment of Biopharmaceutical Sciences, University of Illinois, 833 S. Wood Street, Chicago, IL 60612, USA.
Cheng Yang
Chelsea M Kirkmire
Zaijie Jim Wang
University of Illinois Chicago · US

Funding

Protein kinase mechanisms for chronic pain in sickle cell diseaseR01HL098141 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI WANG, ZAIJIE JIM · 2009 to 2017
$2.6M
Pharmacological Sciences Predoctoral Training ProgramT32GM070388 · NIGMS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI MALIK, ASRAR B. · 2005 to 2009
$795k
Academic Career Development in Botanical Dietary SupplementsK07AT003647 · NCCIH · UNIVERSITY OF ILLINOIS AT CHICAGO · PI WANG, ZAIJIE JIM · 2007 to 2012
$676k
NCCIH NIH HHS K07 AT003647NHLBI NIH HHS R01 HL098141NIGMS NIH HHS GM070388NIGMS NIH HHS T32 GM070388
6 · The paper itself

Abstract

MicroRNA has emerged as a critical regulator of neuronal functions. This study aimed to test whether let-7 microRNAs can regulate the mu opioid receptor (MOR) and opioid tolerance. Employing bioinformatics, we identified a let-7 binding site in the 3'-untranslated region (UTR) of MOR mRNA, which was experimentally confirmed as a direct target of let-7. The repressive regulation of MOR by let-7 was revealed using a LNA-let-7 inhibitor to knockdown let-7 in SH-SY5Y cells. Conversely, morphine significantly upregulated let-7 expression in SH-SY5Y cells and in a mouse model of opioid tolerance. The LNA-let-7 inhibitor decreased brain let-7 levels and partially attenuated opioid antinociceptive tolerance in mice. Although chronic morphine treatment did not change overall MOR transcript, polysome-associated mRNA declined in a let-7-dependent manner. let-7 was identified as a mediator translocating and sequestering MOR mRNA to P-bodies, leading to translation repression. These results suggest that let-7 plays an integral role in opioid tolerance.

Indexed as

Analgesics, Opioid3' Untranslated RegionsAnimalsBehavior, AnimalBinding SitesBrainCell LineDose-Response Relationship, DrugDrug ToleranceGene Expression RegulationHumansMiceMice, Inbred ICRMicroRNAsMorphineMutagenesis3' Untranslated RegionsAnalgesics, OpioidMicroRNAsmirnlet7 microRNA, humanMorphineOligodeoxyribonucleotides, AntisenseReceptors, Opioid, muRNA, Messenger

Identifiers

PMID20668208
PMCPMC2943348
OpenAlexW2100258320

What OpenQuestion holds

Textmetadata
LicenceTDM
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.