Evidence map›Paper›PMID 27590500›Full record

ArticleExperimental biology and medicine (Maywood, N.J.)2017

Phosphoinositide 3-kinase/protein kinase B/periostin mediated platelet-derived growth factor-induced cell proliferation and extracellular matrix production in lupus nephritis.

Xue Zhao, Jun Hao, Huijun Duan, Zanhua Rong, Fan Li

Open access · greenAbstract read
In one paragraph

Article in Experimental biology and medicine (Maywood, N.J.), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 15% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Mesangial Cells in Lupus Nephritis.Current rheumatology reports · 2022
    Review
  5. Mesangial cell: A hub in lupus nephritis.Frontiers in immunology · 2022
    Review
  6. Article
  7. Article
  8. The role of periostin in kidney diseases.Central-European journal of immunology · 2021
    Review
  9. Article
  10. Novel Targets for Therapy of Renal Fibrosis.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2019
    Review
  11. Review
  12. An Adaptogen: Withaferin A AmelioratesFrontiers in pharmacology · 2018
    Article
  13. Periostin in kidney diseases.Cellular and molecular life sciences : CMLS · 2017
    Review
  14. Review
  15. Review
  16. Article
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.

Xue Zhao1 Department of Pathology, Hebei Medical University, Shijiazhuang 050017, China.
Jun Hao1 Department of Pathology, Hebei Medical University, Shijiazhuang 050017, China.
Huijun Duan1 Department of Pathology, Hebei Medical University, Shijiazhuang 050017, China.
Zanhua Rong2 Department of Pediatrics, the 2nd Affiliated Hospital of Hebei Medical University, Shijiazhuang 050017, China.
Fan Li1 Department of Pathology, Hebei Medical University, Shijiazhuang 050017, China.
Hebei Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the present study, the effect and mechanism of periostin on renal proliferation and extracellular matrix accumulation of lupus mice were investigated. MRL /lpr mice, known as lupus mice, were revealed to show enhanced periostin, proliferating cell nuclear antigen (PCNA), and extracellular matrix accumulation in the kidney accompanied by increased serum platelet-derived growth factor (PDGF). Again, cultured mouse mesangial cells (MMCs) were treated with PDGF, then periostin, and PCNA and secreted fibronectin were detected. The results showed that intracellular periostin and PCNA were respectively enhanced by 2.691 and 2.308 times in PDGF-treated MMC cells at 6 h after stimulation. In addition, secreted fibronectin was increased by 1.442 times. Next, the transfection of periostin shRNA vector in PDGF-stimulated MMC cells effectively suppressed periostin, PCNA and secreted fibronectin by 45.27%, 47.75%, and 39.95%, compared with PDGF-stimulated cells transfected with control vector. Furthermore, it was found that PDGF increased the expression of phospho-Akt (Ser 473) from 30 min to 6 h in MMCs. LY294002 effectively inhibited phospho-Akt (Ser 473) expression caused by PDGF stimulation. Then, periostin, PCNA, and fibronectin were respectively decreased by 69.61%, 46.00%, and 46.20%. In the end, phosphoinositide 3-kinase/protein kinase B/periostin was suggested to mediate PDGF-induced cell proliferation and extracellular matrix production in lupus nephritis.

Indexed as

AnimalsCell Adhesion MoleculesCell ProliferationCells, CulturedChromonesExtracellular MatrixFemaleFibronectinsGlomerular MesangiumKidneyLupus NephritisMesangial CellsMiceMice, TransgenicMorpholinesPhosphatidylinositol 3-Kinases2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-oneCell Adhesion MoleculesChromonesFibronectinsMorpholinesPhosphatidylinositol 3-KinasesPhosphoinositide-3 Kinase InhibitorsPlatelet-Derived Growth FactorPOSTN protein, humanProliferating Cell Nuclear AntigenProto-Oncogene Proteins c-aktRNA, Small Interferingextracellular matrixlupus nephritisPeriostinphosphoinositide 3-kinase/protein kinase Bplatelet-derived growth factorproliferating cell nuclear antigen

Identifiers

PMID27590500
PMCPMC5167113
OpenAlexW2509239450

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.