Evidence map›Paper›PMID 30426336›Full record

ArticleCellular and molecular neurobiology2019

MiR-20a Plays a Key Regulatory Role in the Repair of Spinal Cord Dorsal Column Lesion via PDZ-RhoGEF/RhoA/GAP43 Axis in Rat.

Tianyi Wang, Bo Li, Xin Yuan, Libin Cui, Zhijie Wang, Yanjun Zhang, Mei Yu, Yucai Xiu, Zheng Zhang, Wenhua Li and 4 more

Open access · greenAbstract read
In one paragraph

Article in Cellular and molecular neurobiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

17 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
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  8. MicroRNAs in spinal cord injury: A narrative review.Frontiers in molecular neuroscience · 2023
    Review
  9. Review
  10. Review
  11. Improved post-stroke spontaneous recovery by astrocytic extracellular vesicles.Molecular therapy : the journal of the American Society of Gene Therapy · 2022
    Article
  12. 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

14 authors at 7 institutions in 1 country.

Tianyi WangDepartment of Orthopedics, The 266th Hospital of the Chinese People's Liberation Army, Chengde, 067000, Hebei, People's Republic of China.ORCID http://orcid.org/0000-0002-7923-3717
Bo LiDepartment of Orthopedics, Tianjin Medical University General Hospital, Tianjin, 300052, People's Republic of China.ORCID http://orcid.org/0000-0003-0022-0583
Xin YuanDepartment of Spine Surgery, Beijing Luhe Hospital, Capital Medical University, Beijing, 100020, People's Republic of China.
Libin CuiDepartment of Spine Surgery, Beijing Luhe Hospital, Capital Medical University, Beijing, 100020, People's Republic of China.
Zhijie WangDepartment of Pediatric Internal Medicine, Affiliated Hospital of Chengde Medical University, Chengde, 067000, Hebei, People's Republic of China.ORCID http://orcid.org/0000-0001-8474-9323
Yanjun ZhangDepartment of Spine Surgery, Beijing Luhe Hospital, Capital Medical University, Beijing, 100020, People's Republic of China.
Mei YuLeukemia Center, Peking Union of Medical College, Institute of Hematology & Hospital of Blood Diseases, Chinese Academy of Medical Sciences, Tianjin, 30020, People's Republic of China.
Yucai XiuDepartment of Orthopedics, The 266th Hospital of the Chinese People's Liberation Army, Chengde, 067000, Hebei, People's Republic of China.
Zheng ZhangDepartment of Orthopedics, The 266th Hospital of the Chinese People's Liberation Army, Chengde, 067000, Hebei, People's Republic of China.
Wenhua LiDepartment of Orthopedics, The 266th Hospital of the Chinese People's Liberation Army, Chengde, 067000, Hebei, People's Republic of China.
Fengyan WangDepartment of Orthopedics, The 266th Hospital of the Chinese People's Liberation Army, Chengde, 067000, Hebei, People's Republic of China.
Xiaoling GuoDepartment of Neurology, The 266th Hospital of the Chinese People's Liberation Army, Chengde, 067000, Hebei, People's Republic of China. 870808116@qq.com.
Xiangyang ZhaoDepartment of General Surgery, The 266th Hospital of the Chinese People's Liberation Army, Chengde, 067000, Hebei, People's Republic of China. wtyjjandt@sina.cn.
Xueming ChenDepartment of Spine Surgery, Beijing Luhe Hospital, Capital Medical University, Beijing, 100020, People's Republic of China. sjxfcd@sina.com.
Chinese People's Liberation Army · CNBeijing Luhe Hospital Affiliated to Capital Medical University · CNChengde Medical University · CNChinese Academy of Medical Sciences & Peking Union Medical College · CNPeople's Liberation Army 401 Hospital · CNThe 309th Hospital of Chinese People's Liberation Army · CNTianjin Medical University General Hospital · CN

Funding

the Beijing Municipal Education Commission General Project KM201710025028The Capital characteristic project Z161100000116064The General Program of Natural Science Foundation of Hebei Province of China H2017101030The Medical Science and Technology Youth Cultivation Project of the Chinese People's Liberation Army 13QNP017The Medical Science and Technology Youth Cultivation Project of the Chinese People's Liberation Army 16QNP074The Public Experiment Training Foundation of Beijing Luhe Hospital, Capital Medical University, China lh201425ShiThe Research and Development of Science and Technology Program Supported by Chengde Government 201606A062
6 · The paper itself

Abstract

Spinal cord injury (SCI) causes sensory dysfunctions such as paresthesia, dysesthesia, and chronic neuropathic pain. MiR-20a facilitates the axonal outgrowth of the cortical neurons. However, the role of miR-20a in the axonal outgrowth of primary sensory neurons and spinal cord dorsal column lesion (SDCL) is yet unknown. Therefore, the role of miR-20a post-SDCL was investigated in rat. The NF-200 immunofluorescence staining was applied to observe whether axonal outgrowth of dorsal root ganglion (DRG) neurons could be altered by miR-20a or PDZ-RhoGEF modulation in vitro. The expression of miR-20a was quantized with RT-PCR. Western blotting analyzed the expression of PDZ-RhoGEF/RhoA/GAP43 axis after miR-20a or PDZ-RhoGEF was modulated. The spinal cord sensory conduction function was assessed by somatosensory-evoked potentials and tape removal test. The results demonstrated that the expression of miR-20a decreased in a time-dependent manner post-SDCL. The regulation of miR-20a modulated the axonal growth and the expression of PDZ-RhoGEF/RhoA/GAP43 axis in vitro. The in vivo regulation of miR-20a altered the expression of miR-20a-PDZ-RhoGEF/RhoA/GAP43 axis and promoted the recovery of ascending sensory function post-SDCL. The results indicated that miR-20a/PDZ-RhoGEF/RhoA/GAP43 axis is associated with the pathophysiological process of SDCL. Thus, targeting the miR-20a/PDZ-RhoGEF /RhoA/GAP43 axis served as a novel strategy in promoting the sensory function recovery post-SCI.

Indexed as

Signal TransductionWound HealingAnimalsFemaleGanglia, SpinalGAP-43 ProteinGuanine Nucleotide Exchange FactorsMicroRNAsNeuritesRats, WistarRecovery of FunctionrhoA GTP-Binding ProteinSensory Receptor CellsSpinal CordSpinal Cord InjuriesUp-RegulationGAP-43 ProteinGuanine Nucleotide Exchange FactorsMicroRNAsMIRN20 microRNA, ratPDZ-RhoGEF, ratrhoA GTP-Binding ProteinDorsal column lesionDorsal root ganglionMicroRNA-20aNeurite growthPDZ-RhoGEFPrimary sensory neuronRhoA

Identifiers

PMID30426336
PMCPMC11469850
OpenAlexW2901393337

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.