Evidence map›Paper›PMID 29915198›Full record

ArticleCell death & disease2018

miR-129 controls axonal regeneration via regulating insulin-like growth factor-1 in peripheral nerve injury.

Hui Zhu, Chengbin Xue, Min Yao, Hongkui Wang, Ping Zhang, Tianmei Qian, Songlin Zhou, Shiying Li, Bin Yu, Yongjun Wang and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 3 pooled it
2.3field-weighted citation impact, top 12% 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

30 citing papers in PubMed, 3 syntheses or guidelines pooled it, 49 citations in OpenAlex.

  1. Pooled it
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  14. IGF/IGF-1R signal pathway in pain: a promising therapeutic target.International journal of biological sciences · 2023
    Review
  15. Evaluation and Comparison of the Effects of Mature Silkworm (Iranian journal of pharmaceutical research : IJPR · 2022
    Article
  16. Review
  17. Review
  18. Article
  19. Effects and molecular mechanisms ofAnnals of translational medicine · 2021
    Article
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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

11 authors at 3 institutions in 1 country.

Hui ZhuJiangsu Clinical Medicine Center of Tissue Engineering and Nerve Injury Repair, Research Center of Clinical Medicine, Affiliated Hospital of Nantong University, 20# Xisi Road, Nantong, Jiangsu, 226001, P.R. China.
Chengbin XueJiangsu Clinical Medicine Center of Tissue Engineering and Nerve Injury Repair, Research Center of Clinical Medicine, Affiliated Hospital of Nantong University, 20# Xisi Road, Nantong, Jiangsu, 226001, P.R. China. xue_chengbin@hotmail.com.
Min YaoKey Laboratory of Neuroregeneration, Ministry of Education and Jiangsu Province, Co-innovation Center of Neuroregeneration, Nantong University, 19# Qixiu Road, Nantong, Jiangsu, 226001, P.R. China.
Hongkui WangKey Laboratory of Neuroregeneration, Ministry of Education and Jiangsu Province, Co-innovation Center of Neuroregeneration, Nantong University, 19# Qixiu Road, Nantong, Jiangsu, 226001, P.R. China.
Ping ZhangKey Laboratory of Neuroregeneration, Ministry of Education and Jiangsu Province, Co-innovation Center of Neuroregeneration, Nantong University, 19# Qixiu Road, Nantong, Jiangsu, 226001, P.R. China.
Tianmei QianKey Laboratory of Neuroregeneration, Ministry of Education and Jiangsu Province, Co-innovation Center of Neuroregeneration, Nantong University, 19# Qixiu Road, Nantong, Jiangsu, 226001, P.R. China.
Songlin ZhouKey Laboratory of Neuroregeneration, Ministry of Education and Jiangsu Province, Co-innovation Center of Neuroregeneration, Nantong University, 19# Qixiu Road, Nantong, Jiangsu, 226001, P.R. China.
Shiying LiKey Laboratory of Neuroregeneration, Ministry of Education and Jiangsu Province, Co-innovation Center of Neuroregeneration, Nantong University, 19# Qixiu Road, Nantong, Jiangsu, 226001, P.R. China.
Bin YuKey Laboratory of Neuroregeneration, Ministry of Education and Jiangsu Province, Co-innovation Center of Neuroregeneration, Nantong University, 19# Qixiu Road, Nantong, Jiangsu, 226001, P.R. China.
Yongjun WangKey Laboratory of Neuroregeneration, Ministry of Education and Jiangsu Province, Co-innovation Center of Neuroregeneration, Nantong University, 19# Qixiu Road, Nantong, Jiangsu, 226001, P.R. China. wyjbs@ntu.edu.cn.
Xiaosong GuJiangsu Clinical Medicine Center of Tissue Engineering and Nerve Injury Repair, Research Center of Clinical Medicine, Affiliated Hospital of Nantong University, 20# Xisi Road, Nantong, Jiangsu, 226001, P.R. China. nervegu@ntu.edu.cn.
Nantong University · CNAffiliated Hospital of Nantong University · CNNanjing University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The microenvironment of peripheral nerve regeneration consists of multiple neurotrophic factors, adhesion molecules, and extracellular matrix molecules, secreted by unique glial cells in the peripheral nerve system (PNS)-Schwann cell (SCs). Following peripheral nerve injury (PNI), local IGF-1 production is upregulated in SCs and denervated muscle during axonal sprouting and regeneration. Regulation of IGF-1/IGF-1R signaling is considered as a potentially targeted therapy of PNI. We previously identified a group of novel miRNAs in proximal nerve following rat sciatic nerve transection. The present work focused on the role of miR-129 in regulation of IGF-1 signaling after sciatic nerve injury. The temporal change profile of the miR-129 expression was negatively correlated with the IGF-1 expression in proximal nerve stump and dorsal root ganglion (DRG) following sciatic nerve transection. An increased expression of miR-129 inhibited proliferation and migration of SCs, and axonal outgrowth of DRG neurons, which was inversely promoted by silencing of the miR-129 expression. The IGF-1 was identified as one of the multiple target genes of miR-129, which exerted negative regulation of IGF-1 by translational suppression. Moreover, knockdown of IGF-1 attenuated the promoting effects of miR-129 inhibitor on proliferation and migration of SCs, and neurite outgrowth of DRG neurons. Overall, our data indicated that miR-129 own the potential to regulate the proliferation and migration of SCs by targeting IGF-1, providing further insight into the regulatory role of miRNAs in peripheral nerve regeneration. The present work not only provides new insight into miR-129 regulation of peripheral nerve regeneration by robust phenotypic modulation of neural cells, but also opens a novel therapeutic window for PNI by mediating IGF-1 production. Our results may provide further experimental basis for translation of the molecular therapy into the clinic.

Indexed as

AnimalsAnimals, NewbornAxonsCells, CulturedGene Expression RegulationHEK293 CellsHumansInsulin-Like Growth Factor IMaleMicroRNAsNerve RegenerationPeripheral Nerve InjuriesRatsRats, Sprague-DawleyInsulin-Like Growth Factor IMicroRNAsMIRN129 microRNA, rat

Identifiers

PMID29915198
PMCPMC6006361
OpenAlexW2808993958

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.