Evidence map›Paper›PMID 33211272›Full record

ArticleNeurochemical research2021

MicroRNA-139-5p Promotes Functional Recovery and Reduces Pain Hypersensitivity in Mice with Spinal Cord Injury by Targeting Mammalian Sterile 20-like Kinase 1.

Panfeng Wang, Yuntong Zhang, Yan Xia, Dayuan Xu, Hongrui Wang, Dong Liu, Shuogui Xu, Yongming Sun

Abstract read
PubMed Publisher
In one paragraph

Article in Neurochemical research, 2021. 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
1.0field-weighted citation impact, top 23% 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, 13 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. The role of non-coding RNAs in neuropathic pain.Pflugers Archiv : European journal of physiology · 2024
    Review
  7. Review
  8. Review
  9. MST1/2 in inflammation and immunity.Cell adhesion & migration · 2023
    Review
  10. Article
  11. Review
  12. 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

8 authors at 4 institutions in 1 country.

Panfeng Wang *War and Traumat Emergency Centre, Changhai Hospital, Navy Military Medical University, Changhai Road 168, Shanghai, 200433, China.
Yuntong Zhang *War and Traumat Emergency Centre, Changhai Hospital, Navy Military Medical University, Changhai Road 168, Shanghai, 200433, China.
Yan XiaWar and Traumat Emergency Centre, Changhai Hospital, Navy Military Medical University, Changhai Road 168, Shanghai, 200433, China.
Dayuan XuWar and Traumat Emergency Centre, Changhai Hospital, Navy Military Medical University, Changhai Road 168, Shanghai, 200433, China.
Hongrui WangWar and Traumat Emergency Centre, Changhai Hospital, Navy Military Medical University, Changhai Road 168, Shanghai, 200433, China.
Dong LiuDepartment of Orthopedics, The Second Affiliated Hospital of Soochow University, Sanxiang Road 1055, Suzhou, 215004, China.
Shuogui XuWar and Traumat Emergency Centre, Changhai Hospital, Navy Military Medical University, Changhai Road 168, Shanghai, 200433, China.
Yongming SunDepartment of Orthopedics, The Second Affiliated Hospital of Soochow University, Sanxiang Road 1055, Suzhou, 215004, China. bzswy@163.com.
Second Military Medical University · CNChanghai Hospital · CNSoochow University · CNSecond Affiliated Hospital of Soochow University · CN

Funding

Planned Science and Technology Project of Suzhou city SS201611
6 · The paper itself

Abstract

Currently, there is no cure for spinal cord injury (SCI), a heavy burden on patients physiology and psychology. We found that microRNA-139-5p (miR-139-5p) expression was significantly downregulated in damaged spinal cords in mice. So, we aimed to test the effect of treatment with miR-139-5p on functional recovery and neuropathic pain in mice with SCI and investigate the underlying mechanism. The luciferase reporter assay revealed that miR-139-5p directly targeted mammalian sterile 20-like kinase 1 (Mst1), and miR-139-5p treatment suppressed Mst1 protein expression in damaged spinal cords of mice. Wild-type mice and Mst1(-/-) mice were exposed to SCI and treated with miR-139-5p agomir via intrathecal infusion. Treatment of SCI mice with miR-139-5p accelerated locomotor functional recovery, reduced hypersensitivities to mechanical and thermal stimulations, and promoted neuronal survival in damaged spinal cords. Treatment with miR-139-5p enhanced phosphorylation of adenosine monophosphate-activated protein kinase alpha (AMPKα), improved mitochondrial function, and suppressed NF-κB-related inflammation in damaged spinal cords. Deficiency of Mst1 had similar benefits in mice with SCI. Furthermore, miR-139-5p treatment did not provide further protection in Mst1(-/-) mice against SCI. In conclusion, miR-139-5p treatment enhanced functional recovery and reduced pain hypersensitivity in mice with SCI, possibly through targeting Mst1.

Indexed as

AnimalsDown-RegulationGene Knockout TechniquesHippo KinasesInflammationLocomotionMaleMiceMice, Inbred C57BLMice, KnockoutMicroRNAsMitochondriaMotor NeuronsNeuralgiaProtein Serine-Threonine KinasesRecovery of FunctionHippo KinasesMicroRNAsMIRN139 microRNA, mouseProtein Serine-Threonine KinasesStk4 protein, mouseAdenosine monophosphate-activated protein kinaseAllodyniaInflammationMitochondrial function

Identifiers

PMID33211272
OpenAlexW3105892963

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.