Evidence map›Paper›PMID 14961072›Full record

ArticleGene therapy2004

Transcription factor decoy for AP-1 reduces mesangial cell proliferation and extracellular matrix production in vitro and in vivo.

J D Ahn, R Morishita, Y Kaneda, H J Kim, Y D Kim, H J Lee, K U Lee, J Y Park, Y H Kim, K K Park and 5 more

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In one paragraph

Article in Gene therapy, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

21 citing papers in PubMed, 48 citations in OpenAlex.

  1. Trial
  2. Role of activator protein-1 in the transcription of interleukin-5 gene regulated by protein kinase C signal in asthmatic human T lymphocytes.Journal of Huazhong University of Science and Technology. Medical sciences = Hua zhong ke ji da xue xue bao. Yi xue Ying De wen ban = Huazhong keji daxue xuebao. Yixue Yingdewen ban · 2005
    Trial
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Urotensin II-induced store-operated CaScientific reports · 2017
    Article
  9. Review
  10. Article
  11. Article
  12. Novel therapeutic approaches to lupus glomerulonephritis: translating animal models to clinical practice.American journal of kidney diseases : the official journal of the National Kidney Foundation · 2011
    Review
  13. Protective Effects of Luteolin on Diabetic Nephropathy in STZ-Induced Diabetic Rats.Evidence-based complementary and alternative medicine : eCAM · 2011
    Article
  14. Review
  15. Article
  16. Article
  17. 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

15 authors at 4 institutions in 1 country.

J D AhnDepartment of Microbiology, Kyungpook National University, Taegu, Korea.
R Morishita
Y Kaneda
H J Kim
Y D Kim
H J Lee
K U Lee
J Y Park
Y H Kim
K K Park
Y C Chang
K H Yoon
H S Kwon
K G Park
I K Lee
Keimyung University · KRCatholic University of Korea · KRKyungpook National University · KRUniversity of Ulsan · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diabetic nephropathy is characterized by an expansion of glomerular mesangium, caused by mesangial cell proliferation and excessive accumulation of extracellular matrix (ECM) proteins, which eventually leads to glomerulosclerosis and renal failure. Activator protein-1 (AP-1), a transcription factor, is implicated in the transcriptional regulation of a wide range of genes participating in cell proliferation and ECM production. This investigation was undertaken to test the hypothesis that AP-1 plays an important role in ECM gene expression, and to develop a molecular therapeutic strategy based on decoy oligodeoxynucleotides (ODN). In this report, we show that transfection with AP-1 decoy ODN strongly inhibits high glucose- and angiotensin II-induced cell proliferation and expression of ECM genes in cultured mesangial cells in vitro. Administration of AP-1 decoy ODN into streptozotocin-induced diabetic rat kidney in vivo using the hemagglutinating virus of Japan (HVJ)-liposome method virtually abolished TGF-beta1 and plasminogen activator inhibitor-1 expression. Our results collectively indicate that AP-1 activation is crucial for mesangial cell proliferation and ECM production in response to high glucose and angiotensin II. Moreover, use of stable AP-1 decoy ODN combined with the highly effective HVJ-liposome method provides a novel potential molecular therapeutic strategy for the prevention of diabetic nephropathy.

Indexed as

Angiotensin IIAnimalsBase SequenceCell DivisionDiabetic NephropathiesExtracellular MatrixGene ExpressionGenetic TherapyGlomerular MesangiumGlucoseMaleMolecular Sequence DataOligodeoxyribonucleotidesRatsRats, Sprague-DawleyTranscription Factor AP-1Angiotensin IIGlucoseOligodeoxyribonucleotidesTranscription Factor AP-1

Identifiers

PMID14961072
OpenAlexW1972932538

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.