Evidence map›Paper›PMID 31243340›Full record

ArticleLaboratory investigation; a journal of technical methods and pathology2019

Promotion of β-catenin/Foxo1 signaling ameliorates renal interstitial fibrosis.

Padmashree Rao, Min Pang, Xi Qiao, Hong Yu, Hailong Wang, Ying Yang, Xiaojun Ren, Min Hu, Titi Chen, Qi Cao and 10 more

Open access · hybridAbstract read
PubMed Publisher
In one paragraph

Article in Laboratory investigation; a journal of technical methods and pathology, 2019. 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
1.5field-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

21 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Methods to Study Structure and Dynamics of FOXO Proteins.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. FOXOs: masters of the equilibrium.The FEBS journal · 2022
    Review
  11. Article
  12. Article
  13. PSC-MSC-Derived Exosomes Protect against Kidney FibrosisInternational journal of stem cells · 2021
    Article
  14. Article
  15. Article
  16. The Role of Macrophages in Kidney Fibrosis.Frontiers in physiology · 2021
    Review
  17. Editorial: TGF-β in Human Disease: Friend or Foe?Frontiers in cell and developmental biology · 2021
    Article
  18. Epigenetic Histone Modifications in the Pathogenesis of Diabetic Kidney Disease.Diabetes, metabolic syndrome and obesity : targets and therapy · 2021
    Review
  19. Article
  20. 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

20 authors at 5 institutions in 2 countries.

Padmashree RaoCentre for Transplantation and Renal Research, The University of Sydney at The Westmead Institute for Medical Research, Sydney, Australia.
Min PangCentre for Transplantation and Renal Research, The University of Sydney at The Westmead Institute for Medical Research, Sydney, Australia.
Xi QiaoCentre for Transplantation and Renal Research, The University of Sydney at The Westmead Institute for Medical Research, Sydney, Australia.
Hong YuCentre for Transplantation and Renal Research, The University of Sydney at The Westmead Institute for Medical Research, Sydney, Australia.
Hailong WangCentre for Transplantation and Renal Research, The University of Sydney at The Westmead Institute for Medical Research, Sydney, Australia.
Ying YangCentre for Transplantation and Renal Research, The University of Sydney at The Westmead Institute for Medical Research, Sydney, Australia.
Xiaojun RenCentre for Transplantation and Renal Research, The University of Sydney at The Westmead Institute for Medical Research, Sydney, Australia.
Min HuCentre for Transplantation and Renal Research, The University of Sydney at The Westmead Institute for Medical Research, Sydney, Australia.
Titi ChenCentre for Transplantation and Renal Research, The University of Sydney at The Westmead Institute for Medical Research, Sydney, Australia.
Qi CaoCentre for Transplantation and Renal Research, The University of Sydney at The Westmead Institute for Medical Research, Sydney, Australia.
Yiping WangCentre for Transplantation and Renal Research, The University of Sydney at The Westmead Institute for Medical Research, Sydney, Australia.
Matloob KhushiChildren's Medical Research Institute, The University of Sydney, Sydney, Australia.
Geoff ZhangChildren's Hospital at Westmead, Sydney, Australia.
Yuan Min WangChildren's Hospital at Westmead, Sydney, Australia.
Chow Heok P'ngWestmead Hospital, Sydney, Australia.
Brian NankivellWestmead Hospital, Sydney, Australia.
Vincent W LeeCentre for Transplantation and Renal Research, The University of Sydney at The Westmead Institute for Medical Research, Sydney, Australia.
Stephen I AlexanderChildren's Hospital at Westmead, Sydney, Australia.
Guoping ZhengCentre for Transplantation and Renal Research, The University of Sydney at The Westmead Institute for Medical Research, Sydney, Australia. guoping.zheng@sydney.edu.au.
David C HarrisCentre for Transplantation and Renal Research, The University of Sydney at The Westmead Institute for Medical Research, Sydney, Australia.
The University of Sydney · AUWestmead Institute for Medical Research · AUWestmead Hospital · AUChildren's Hospital at Westmead · AUShanxi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transforming growth factor β (TGF-β) is the key cytokine involved in causing fibrosis through cross-talk with major profibrotic pathways. However, inhibition of TGF-β to prevent fibrosis would also abrogate its anti-inflammatory and wound-healing effects. β-catenin is a common co-factor in most TGF-β signaling pathways. β-catenin binds to T-cell factor (TCF) to activate profibrotic genes and binds to Forkhead box O (Foxo) to promote cell survival under oxidative stress. Using a proximity ligation assay in human kidney biopsies, we found that β-catenin/Foxo interactions were higher in kidney with little fibrosis, whereas β-catenin/TCF interactions were upregulated in the kidney of patients with fibrosis. We hypothesised that β-catenin/Foxo is protective against kidney fibrosis. We found that Foxo1 protected against rhTGF-β1-induced profibrotic protein expression using a CRISPR/cas9 knockout of Foxo1 or TCF1 in murine kidney tubular epithelial C1.1 cells. Co-administration of TGF-β with a small molecule inhibitor of β-catenin/TCF (ICG-001), protected against kidney fibrosis in unilateral ureteral obstruction. Collectively, our human, animal and in vitro findings suggest β-catenin/Foxo as a therapeutic target in kidney fibrosis.

Indexed as

Animalsbeta CateninBridged Bicyclo Compounds, HeterocyclicCell LineDisease Models, AnimalFibrosisForkhead Box Protein O1Gene Knockout TechniquesHepatocyte Nuclear Factor 1-alphaHumansKidneyKidney DiseasesMaleMicePyrimidinonesSignal Transductionbeta CateninBridged Bicyclo Compounds, HeterocyclicCTNNB1 protein, humanCTNNB1 protein, mouseForkhead Box Protein O1FOXO1 protein, humanFoxo1 protein, mouseHepatocyte Nuclear Factor 1-alphaHNF1A protein, humanHnf1a protein, mouseICG 001PyrimidinonesTransforming Growth Factor beta1

Identifiers

PMID31243340
OpenAlexW2954314387

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.