Evidence map›Paper›PMID 29633273›Full record

ArticleJournal of cellular physiology2018

NEAT1 contributes to neuropathic pain development through targeting miR-381/HMGB1 axis in CCI rat models.

Lie-Xin Xia, Chengming Ke, Jing-Min Lu

Abstract read
In one paragraph

Article in Journal of cellular physiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed, 1 pooled it
6.4field-weighted citation impact, top 3% 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

51 citing papers in PubMed, 1 synthesis or guideline pooled it, 75 citations in OpenAlex.

  1. Pooled it
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  7. The role of non-coding RNAs in neuropathic pain.Pflugers Archiv : European journal of physiology · 2024
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  14. Identification and coregulation pattern analysis of long noncoding RNAs following subacute spinal cord injury.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2022
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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

3 authors at 2 institutions in 1 country.

Lie-Xin XiaDepartment of Neurology, First People's Hospital of Jingzhou, First Affiliated Hospital of Yangtze University, Jingzhou, Hubei, P.R. China.
Chengming KeDepartment of Neurology, First People's Hospital of Jingzhou, First Affiliated Hospital of Yangtze University, Jingzhou, Hubei, P.R. China.
Jing-Min LuDepartment of Neurology, Huai'an Second People's Hospital, The Affiliated Huai'an Hospital of Xuzhou Medical University, Huai'an, P. R. China.ORCID http://orcid.org/0000-0002-5465-8727
Yangtze University · CNXuzhou Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

LncRNAs have been recognized as significant regulators in various diseases including neuropathic pain. Although the lncRNA NEAT1 has been reported to be involved in multiple cancers, its biological functions in neuropathic pain still remain unknown. In our present study, a chronic constriction injury (CCI) rat model was established and we found that NEAT1 was greatly upregulated in the spinal cord tissues of CCI rats. Knockdown of NEAT1 can repress neuropathic pain behaviors including mechanical and thermal hyperalgesia. In addition, NEAT1 downregulation inhibited neuroinflammation via inhibiting IL-6, IL-1β, and tumor necrosis factor (TNF)-α in CCI rats. We also observed that miR-381 was decreased significantly in CCI rats. By using bioinformatics analysis, miR-381 was predicted to be a microRNA target of NEAT1, which indicated a negative correlation between miR-381 and NEAT1. Inhibition of NEAT1 can induce miR-381 expression in CCI rats, which indicated a negative correlation between NEAT1 and miR-381. HMGB1, as a downstream target gene of miR-381 was observed to be dramatically increased in CCI rats. miR-381 can modulate HMGB1 expression negatively and meanwhile, NEAT1 was able to regulate HMGB1 through sponging miR-381. Downregulation of HMGB1 can inhibit neuropathic pain behaviors which can be reversed by miR-381 inhibitors. Taken these together, it was indicated that NEAT1 can induce neuropathic pain development in CCI rats via regulating miR-381/HMGB1 axis.

Indexed as

Signal TransductionAnimalsBase SequenceChronic DiseaseConstriction, PathologicDisease Models, AnimalDisease ProgressionDown-RegulationFemaleHEK293 CellsHMGB1 ProteinHumansInflammationMicroRNAsNeuralgiaRats, Sprague-DawleyHMGB1 ProteinMicroRNAsMIRN381 microRNA, ratRNA, Long NoncodingHMGB1miR-381NEAT1neuropathic pain

Identifiers

PMID29633273
PMCPMC13482416
OpenAlexW2806199088

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.