Evidence map›Paper›PMID 25063219›Full record

ArticleMolecular and cellular biochemistry2014

MiRNA-26b inhibits the proliferation, migration, and epithelial-mesenchymal transition of lens epithelial cells.

Ning Dong, Bing Xu, Silvia R Benya, Xin Tang

RetractedAbstract readRetracted Publication
PubMed Publisher
In one paragraph

Article in Molecular and cellular biochemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.7field-weighted citation impact, top 8% 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, 38 citations in OpenAlex.

  1. Review
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  9. miRNA-26b suppresses the TGF-β2-induced progression of HLE-B3 cellsInternational journal of ophthalmology · 2021
    Article
  10. Article
  11. Long Noncoding RNA NEAT1 Regulates TGF-BioMed research international · 2020
    Article
  12. Article
  13. LncRNA FEZF1-AS1 Promotes TGF-Journal of ophthalmology · 2019
    Article
  14. Article
  15. Article
  16. [Overpression of miR-29b suppresses the proliferation and induces apoptosis of cholangiocarcinoma cells].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2018
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 4 institutions in 2 countries.

Ning DongDepartment of Ophthalmology, Beijing Shijitan Hospital, Capital Medical University, Beijing, People's Republic of China.
Bing Xu
Silvia R Benya
Xin Tang
Capital Medical University · CNCapital University · USThe University of Texas Medical Branch at Galveston · USTianjin Medical University Eye Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNAs (miRNAs) are a class of small endogenous gene regulators that play important roles in various developmental and pathological processes. However, little is known about the precise identity and functions of miR-26b in posterior capsule opacification (PCO). In this study, we report that the expression of miR-26b is decreased in human PCO-attached lens epithelial cells (LECs) and SRA01/04 cells in the presence of TGF-β2. Overexpression of miR-26b inhibited the proliferation of LECs based on MTT assays and BrdU incorporation assays. In addition, the overexpression of miR-26b inhibited the migration ability of LECs, as shown by wound-healing and transwell migration assays. The overexpression of miR-26b increased the level of the lens epithelial marker E-cadherin and reduced the levels of mesenchymal-related proteins, such as fibronectin, a-SMA, and type I collagen, in SRA01/04 cells in the presence of TGF-β2. Furthermore, the upregulation of E-cadherin and downregulation of mesenchymal-related proteins were induced in human PCO-attached LECs transfected with miR-26b mimics. We further demonstrated that Smad4 and COX-2 are targets of miR-26b in LECs using luciferase reporter assays. These data reveal that miR-26b can inhibit the proliferation, migration, and EMT of lens epithelial cells, and restoration of miRNA-26b may be a potential, novel therapeutic target for the prevention and treatment of posterior capsule opacification.

Indexed as

CadherinsCapsule OpacificationCell LineCell MovementCell ProliferationCyclooxygenase 2Epithelial CellsEpithelial-Mesenchymal TransitionGene Expression RegulationHumansLens, CrystallineMicroRNAsPosterior Capsule of the LensSmad4 ProteinTransforming Growth Factor beta2CadherinsCyclooxygenase 2MicroRNAsMIRN26 microRNA, humanPTGS2 protein, humanSmad4 ProteinSMAD4 protein, humanTransforming Growth Factor beta2

Identifiers

PMID25063219
OpenAlexW2013898919

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.