Evidence map›Paper›PMID 28652727›Full record

ArticleInternational journal of nanomedicine2017

Biodegradable and biocompatible cationic polymer delivering microRNA-221/222 promotes nerve regeneration after sciatic nerve crush.

Jialin Song, Xueyang Li, Yingli Li, Junyi Che, Xiaoming Li, Xiaotian Zhao, Yinghui Chen, Xianyou Zheng, Weien Yuan

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

15 citing papers in PubMed, 25 citations in OpenAlex.

  1. Observational
  2. Review
  3. [Gene silencing of Nemo-like kinase promotes neuralized tissue engineered bone regeneration].Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences · 2025
    Article
  4. Article
  5. Remyelination in multiple sclerosis from the miRNA perspective.Frontiers in molecular neuroscience · 2023
    Review
  6. Review
  7. Delivery of therapeutic miRNA using polymer-based formulation.Drug delivery and translational research · 2019
    Review
  8. Review
  9. Article
  10. Article
  11. Non-viral based miR delivery and recent developments.European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V · 2018
    Review
  12. Article
  13. Article
  14. Review
  15. Article
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

9 authors at 3 institutions in 2 countries.

Jialin SongDepartment of Orthopedics, Shanghai Jiao Tong University Affiliated Sixth People's Hospital.
Xueyang LiDepartment of Plastic and Reconstructive Surgery, Xuzhou Medical College Affiliated Hospital, Xuzhou, Jiangsu.
Yingli LiDepartment of Plastic Surgery, The General Hospital of Jinan Military Command, Jinan, Shandong.
Junyi CheSchool of Pharmacy, Shanghai Jiao Tong University.
Xiaoming LiSchool of Pharmacy, Shanghai Jiao Tong University.
Xiaotian ZhaoSchool of Pharmacy, Shanghai Jiao Tong University.
Yinghui ChenDepartment of Neurology, Jinshan Hospital, Fudan University, JinShan District, Shanghai, People's Republic of China.
Xianyou ZhengDepartment of Orthopedics, Shanghai Jiao Tong University Affiliated Sixth People's Hospital.
Weien YuanSchool of Pharmacy, Shanghai Jiao Tong University.
Shanghai Jiao Tong University · CNXuzhou Medical College · CNSecond Military Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNA (miRNA) has great potential to treat a wide range of illnesses by regulating the expression of eukaryotic genes. Biomaterials with high transfection efficiency and low toxicity are needed to deliver miRNA to target cells. In this study, a biodegradable and biocompatible cationic polymer (PDAPEI) was synthetized from low molecular weight polyethyleneimine (PEI1.8kDa) cross-linked with 2,6-pyridinedicarboxaldehyde. PDAPEI showed a lower cytotoxicity and higher transfection efficiency than PEI25kDa in transfecting miR-221/222 into rat Schwann cells (SCs). The upregulation of miR-221/222 in SCs promoted the expression of nerve growth factor and myelin basic protein in vitro. The mouse sciatic nerve crush injury model was used to evaluate the effectiveness of PDAPEI/miR-221/222 complexes for nerve regeneration in vivo. The results of electrophysiological tests, functional assessments, and histological and immunohistochemistry analyses demonstrated that PDAPEI/miR-221/222 complexes significantly promoted nerve regeneration after sciatic nerve crush, specifically enhancing remyelination. All these results show that the use of PDAPEI to deliver miR-221/222 may provide a safe therapeutic means of treating nerve crush injury and may help to overcome the barrier of biomaterial toxicity and low efficiency often encountered during medical intervention.

Indexed as

AnimalsBiocompatible MaterialsCationsDisease Models, AnimalMaleMiceMicroRNAsMyelin Basic ProteinNanoparticlesNerve CrushNerve Growth FactorNerve RegenerationPolymersRatsRats, Sprague-DawleySchwann CellsBiocompatible MaterialsCationsMicroRNAsMyelin Basic ProteinNerve Growth FactorPolymersmiR-221/222nerve regenerationPDAPEIremyelination

Identifiers

PMID28652727
PMCPMC5473607
OpenAlexW2621967149

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.