Evidence map›Paper›PMID 35865316›Full record

ReviewFrontiers in endocrinology2022

MicroRNA-21: A Critical Pathogenic Factor of Diabetic Nephropathy.

Shuijiao Liu, Weizhou Wu, Jian Liao, Fuqin Tang, Ge Gao, Jing Peng, Xiujing Fu, Yuqin Zhan, Zhihui Chen, Weifang Xu and 1 more

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in endocrinology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
4.1field-weighted citation impact, top 4% 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

25 citing papers in PubMed, 47 citations in OpenAlex.

  1. Review
  2. Epigenetic regulation in a high-sugar environment (Review).International journal of molecular medicine · 2026
    Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Review
  10. Article
  11. Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2025
    Article
  12. Review
  13. Targeting Macrophages: Therapeutic Approaches in Diabetic Kidney Disease.International journal of molecular sciences · 2024
    Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. 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

11 authors at 3 institutions in 1 country.

Shuijiao LiuDepartment of Endocrinology & Department of Gastroenterology, Taizhou Central Hospital (Taizhou University Hospital), Taizhou, China.
Weizhou WuDepartment of Urology, Maoming People's Hospital, Maoming, China.
Jian LiaoDepartment of Nephrology, Jiaxing Hospital of Traditional Chinese Medicine, Jiaxing, China.
Fuqin TangNursing Department, Taizhou Central Hospital (Taizhou University Hospital), Taizhou, China.
Ge GaoDepartment of Clinical Medical School, Taizhou University, Taizhou, China.
Jing PengDepartment of Clinical Medical School, Taizhou University, Taizhou, China.
Xiujing FuDepartment of Clinical Medical School, Taizhou University, Taizhou, China.
Yuqin ZhanDepartment of Clinical Medical School, Taizhou University, Taizhou, China.
Zhihui ChenDepartment of Clinical Medical School, Taizhou University, Taizhou, China.
Weifang XuDepartment of Orthopedics, Taizhou Central Hospital (Taizhou University Hospital), Taizhou, China.
Shankun ZhaoDepartment of Urology, Taizhou Central Hospital (Taizhou University Hospital), Taizhou, China.
Taizhou University · CNTaizhou Central Hospital · CNFirst Hospital of Jiaxing · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diabetic nephropathy (DN), one of the most common and intractable microvascular complications of diabetes, is the main cause of terminal renal disease globally. MicroRNA-21 (miR-21) is a kind of miRNA early identified in human circulation and tissues. Mounting studies have demonstrated that miR-21 plays an important role in the development and progression of DN. This collaborative review aimed to present a first attempt to capture the current evidence on the relationship between miR-21 and DN. After a systematic search, 29 relevant studies were included for comprehensively and thoroughly reviewing. All these eligible studies reported that miR-21 was up-regulated in DN, whether in serum or renal tissues of human or animal models. MiR-21 exhibited its pathogenic roles in DN by forming a complex network with targeted genes (e.g. MMP-9, Smad7, TIMP3, Cdk6, FOXO1, IMP3, and MMP2) and the signaling cascades (e.g. Akt/TORC1 signaling axis, TGF-β/NF-κB signaling pathways, TGF-β/SMAD pathway, CADM1/STAT3 signaling, and AGE-RAGE regulatory cascade), which resulted in epithelial-to-mesenchymal transition, extracellular matrix deposition, cytoskeletal remodeling, inflammation, and fibrosis. This review highlights that miR-21 is a pivotal pathogenic factor in the development of DN. It may serve as an attractive potential diagnostic, prognostic, and predictive biomarker for DN in clinical practice after further confirmation of the clinicopathological features and molecular mechanisms of miR-21-mediated DN.

Indexed as

Diabetes MellitusDiabetic NephropathiesMicroRNAsAnimalsCell Adhesion Molecule-1FibrosisHumansTransforming Growth Factor betaVirulence FactorsCADM1 protein, humanCell Adhesion Molecule-1MicroRNAsMIRN21 microRNA, humanTransforming Growth Factor betaVirulence Factorsbiomarkerdiabetic nephropahy (DN)mechanismMicroRNA-21target

Identifiers

PMID35865316
PMCPMC9294636
OpenAlexW4283817013

What OpenQuestion holds

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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.