Evidence map›Paper›PMID 26064952›Full record

ArticleBioMed research international2015

Paricalcitol Inhibits Aldosterone-Induced Proinflammatory Factors by Modulating Epidermal Growth Factor Receptor Pathway in Cultured Tubular Epithelial Cells.

Jose L Morgado-Pascual, Sandra Rayego-Mateos, Jose M Valdivielso, Alberto Ortiz, Jesus Egido, Marta Ruiz-Ortega

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.8field-weighted citation impact, top 17% 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

13 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Review
  3. Chronic Kidney Disease and Cancer: Inter-Relationships and Mechanisms.Frontiers in cell and developmental biology · 2022
    Review
  4. Review
  5. Review
  6. Novel Evidence of Acute Kidney Injury in COVID-19.Journal of clinical medicine · 2020
    Review
  7. Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. 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

6 authors at 4 institutions in 1 country.

Jose L Morgado-PascualCellular Biology in Renal Diseases Laboratory, IIS-Fundación Jimenez Diaz, Universidad Autónoma Madrid (UAM), 28040 Madrid, Spain ; REDINREN, Madrid, Spain.
Sandra Rayego-MateosCellular Biology in Renal Diseases Laboratory, IIS-Fundación Jimenez Diaz, Universidad Autónoma Madrid (UAM), 28040 Madrid, Spain ; REDINREN, Madrid, Spain.
Jose M ValdivielsoREDINREN, Madrid, Spain ; Department of Experimental Nephrology, Universitat de Lleida/Institut de Recerca Biomèdica de Lleida, 25198 Lleida, Spain.
Alberto OrtizREDINREN, Madrid, Spain ; Dialysis Unit, IIS-Fundación Jiménez Díaz, School of Medicine, UAM, Madrid, Spain ; Institute of Renal Research Queen Sophia (IRSIN), Spain.
Jesus EgidoInstitute of Renal Research Queen Sophia (IRSIN), Spain ; Division of Nephrology and Hypertension, IIS-Fundación Jiménez Díaz, UAM, Madrid, Spain ; Spanish Biomedical Research Centre in Diabetes and Associated Metabolic Disorders (CIBERDEM), Spain.
Marta Ruiz-OrtegaCellular Biology in Renal Diseases Laboratory, IIS-Fundación Jimenez Diaz, Universidad Autónoma Madrid (UAM), 28040 Madrid, Spain ; REDINREN, Madrid, Spain.
Spanish Clinical Research Network · ESUniversidad Autónoma de Madrid · ESHospital Universitario Fundación Jiménez Díaz · ESUniversitat de Lleida · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic kidney disease is characterized by Vitamin D deficiency and activation of the renin-angiotensin-aldosterone system. Increasing data show that vitamin D receptor agonists (VDRAs) exert beneficial effects in renal disease and possess anti-inflammatory properties, but the underlying mechanism remains unknown. Emerging evidence suggests that "a disintegrin and metalloproteinase" (ADAM)/epidermal growth factor receptor (EGFR) signalling axis contributes to renal damage. Aldosterone induces EGFR transactivation regulating several processes including cell proliferation and fibrosis. However, data on tubular epithelial cells is scarce. We have found that, in cultured tubular epithelial cells, aldosterone induced EGFR transactivation via TGF-α/ADAM17. Blockade of the TGF-α/ADAM17/EGFR pathway inhibited aldosterone-induced proinflammatory gene upregulation. Moreover, among the potential downstream mechanisms, we found that TGF-α/ADAM17/EGFR inhibition blocked ERK and STAT-1 activation in response to aldosterone. Next, we investigated the involvement of TGF-α/ADAM17/EGFR axis in VDRA anti-inflammatory effects. Preincubation with the VDRA paricalcitol inhibited aldosterone-induced EGFR transactivation, TGF-α/ADAM-17 gene upregulation, and downstream mechanisms, including proinflammatory factors overexpression. In conclusion, our data suggest that the anti-inflammatory actions of paricalcitol in tubular cells could depend on the inhibition of TGF-α/ADAM17/EGFR pathway in response to aldosterone, showing an important mechanism of VDRAs action.

Indexed as

ADAM17 ProteinADAM ProteinsAldosteroneCell LineCell ProliferationEpithelial CellsErbB ReceptorsErgocalciferolsGene Expression RegulationHumansInflammationKidney TubulesReceptors, CalcitriolRenal Insufficiency, ChronicRenin-Angiotensin SystemSignal TransductionADAM17 ProteinADAM17 protein, humanADAM ProteinsAldosteroneEGFR protein, humanErbB ReceptorsErgocalciferolsparicalcitolReceptors, CalcitriolSTAT1 protein, humanSTAT1 Transcription FactorTransforming Growth Factor alpha

Identifiers

PMID26064952
PMCPMC4438184
OpenAlexW1779486602

What OpenQuestion holds

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Registered trials

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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.