Evidence map›Paper›PMID 20501654›Full record

ArticleThe Journal of biological chemistry2010

Identification of microRNA-93 as a novel regulator of vascular endothelial growth factor in hyperglycemic conditions.

Jianyin Long, Yin Wang, Wenjian Wang, Benny H J Chang, Farhad R Danesh

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 156 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
156citing papers in PubMed, 4 pooled it
9.1field-weighted citation impact, top 2% 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

156 citing papers in PubMed, 4 syntheses or guidelines pooled it, 268 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Article
  6. Article
  7. MicroRNAs in diabetes mellitus.Journal of diabetes and metabolic disorders · 2025
    Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. The Role of MicroRNA in the Pathogenesis of Diabetic Nephropathy.International journal of molecular sciences · 2023
    Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. Review

96 more citing papers are in PubMed but not listed here.

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

5 authors at 1 institution in 1 country.

Jianyin LongDivision of Nephrology, Department of Medicine, Baylor College of Medicine, Houston, Texas 77030, USA.
Yin Wang
Wenjian Wang
Benny H J Chang
Farhad R Danesh
Baylor College of Medicine · US

Funding

MicroRNA In Diabetic NephropathyR01DK091310 · NIDDK · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI DANESH, FARHAD R · 2011 to 2024
$5.3M
Role of Rho Kinases in Diabetic NephropathyR01DK078900 · NIDDK · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI DANESH, FARHAD R · 2009 to 2024
$5.2M
Statins and VEGF-induced cytoskeletal remodelingR01DK067604 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI DANESH, FARHAD R · 2005 to 2009
$1.7M
NIDDK NIH HHS R01 DK067604NIDDK NIH HHS R01DK067604NIDDK NIH HHS R01 DK078900NIDDK NIH HHS R01DK078900NIDDK NIH HHS R01 DK091310
6 · The paper itself

Abstract

Vascular endothelial growth factor (VEGF) is a dimeric glycoprotein that plays a crucial role in microvascular complications of diabetes, including diabetic nephropathy. However, the precise regulatory mechanisms governing VEGF expression in the diabetic milieu are still poorly understood. Here, we provide evidence that microRNA-93 (miR-93) regulates VEGF expression in experimental models of diabetes both in vitro and in vivo. Comparative microRNA expression profile arrays identified miR-93 as a signature microRNA in hyperglycemic conditions. We identified VEGF-A as a putative target of miR-93 in the kidney with a perfect complementarity between miR-93 and the 3'-untranslated region of vegfa in several species. When cotransfected with a luciferase reporter construct containing the mouse vegfa 3'-untranslated region, expression of miR-93 markedly decreased the luciferase activity. We showed that forced expression of miR-93 in cells abrogated VEGF protein secretion. Conversely, anti-miR-93 inhibitors increased VEGF release. Transfection of miR-93 also prevented the effect of high glucose on VEGF downstream targets. Using transgenic mice containing VEGF-LacZ bicistronic transcripts, we found that inhibition of glomerular miR-93 by peptide-conjugated morpholino oligomers elicited increased expression of VEGF. Our findings also indicate that high glucose decreases miR-93 expression by down-regulating the promoter of the host MCM7 gene. Taken together, our findings provide new insights into the role of miR-93 in VEGF signaling pathway and offer a potentially novel target in preventing the progression of diabetic nephropathy.

Indexed as

3' Untranslated RegionsAnimalsBase SequenceCell Cycle ProteinsDiabetes MellitusDNA-Binding ProteinsDose-Response Relationship, DrugDown-RegulationEndothelial CellsGlucoseHeLa CellsHumansHyperglycemiaMiceMicroRNAsMicrovessels3' Untranslated RegionsCell Cycle ProteinsDNA-Binding ProteinsGlucoseMcm7 protein, mouseMicroRNAsMinichromosome Maintenance Complex Component 7Mirn93 microRNA, mousemorpholineMorpholinesNuclear ProteinsPolymersVascular Endothelial Growth Factor Avascular endothelial growth factor A, mouse

Identifiers

PMID20501654
PMCPMC2906336
OpenAlexW2091613784

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.