Evidence map›Paper›PMID 37963889›Full record

ArticleNature communications2023

Epidermal growth factor receptor activation is essential for kidney fibrosis development.

Shirong Cao, Yu Pan, Andrew S Terker, Juan Pablo Arroyo Ornelas, Yinqiu Wang, Jiaqi Tang, Aolei Niu, Sarah Abu Kar, Mengdi Jiang, Wentian Luo and 7 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
6.9field-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

33 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Cell-cell crosstalk in kidney health and disease.Nature reviews. Nephrology · 2026
    Review
  6. Article
  7. Article
  8. Article
  9. Article
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  11. Pharmacological mechanism of active components inFrontiers in pharmacology · 2026
    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

17 authors at 3 institutions in 3 countries.

Shirong Cao *Division of Nephrology and Hypertension, Department of Medicine, Nashville, TN, USA.ORCID 0000-0002-6593-4600
Yu Pan *Division of Nephrology and Hypertension, Department of Medicine, Nashville, TN, USA.
Andrew S TerkerDivision of Nephrology and Hypertension, Department of Medicine, Nashville, TN, USA.
Juan Pablo Arroyo OrnelasDivision of Nephrology and Hypertension, Department of Medicine, Nashville, TN, USA.ORCID 0000-0002-5992-5011
Yinqiu WangDivision of Nephrology and Hypertension, Department of Medicine, Nashville, TN, USA.
Jiaqi TangDivision of Nephrology and Hypertension, Department of Medicine, Nashville, TN, USA.
Aolei NiuDivision of Nephrology and Hypertension, Department of Medicine, Nashville, TN, USA.
Sarah Abu KarDivision of Nephrology and Hypertension, Department of Medicine, Nashville, TN, USA.
Mengdi JiangDivision of Nephrology and Hypertension, Department of Medicine, Nashville, TN, USA.
Wentian LuoDivision of Nephrology and Hypertension, Department of Medicine, Nashville, TN, USA.
Xinyu DongDivision of Nephrology and Hypertension, Department of Medicine, Nashville, TN, USA.ORCID 0000-0002-3017-2634
Xiaofeng FanDivision of Nephrology and Hypertension, Department of Medicine, Nashville, TN, USA.
Suwan WangDivision of Nephrology and Hypertension, Department of Medicine, Nashville, TN, USA.
Matthew H WilsonDivision of Nephrology and Hypertension, Department of Medicine, Nashville, TN, USA.ORCID 0000-0002-3776-8350
Agnes FogoDepartment of Pathology, Microbiology and Immunology, Vanderbilt University Medical Center, Nashville, TN, USA.
Ming-Zhi ZhangDivision of Nephrology and Hypertension, Department of Medicine, Nashville, TN, USA. ming-zhi.zhang@vumc.org.ORCID 0000-0002-0980-2419
Raymond C HarrisDivision of Nephrology and Hypertension, Department of Medicine, Nashville, TN, USA. ray.harris@vumc.org.ORCID 0000-0001-8025-0883
Vanderbilt University · USShanghai Jiao Tong University · CNVanderbilt University Medical Center · US

Funding

Tumor Immunology and Microenvironment Research ProgramP30CA068485 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Ben Ho Park · 1995 to 2026
$172.8M
VANDERBILT UNIVERSITY CTSA FOR PEDIATRIC RESEARCHUL1RR024975 · NCRR · VANDERBILT UNIVERSITY · PI BERNARD, GORDON RAPHAEL · 2007 to 2011
$45.7M
Shop Module CoreP30EY008126 · NEI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI David J. Calkins · 1989 to 2026
$19.6M
The Role of the EGF Receptor in Acute and Chronic Renal InjuryR01DK051265 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI RAYMOND C. HARRIS, Mingzhi Zhang · 1997 to 2026
$10.1M
The role of the innate immune cell cyclooxygenase/prostaglandin system in blood pressureregulationR01DK062794 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI RAYMOND C. HARRIS, Mingzhi Zhang · 2003 to 2026
$9.4M
VANTAGE:Consolidation to create the Vanderbilt Technologies for Advanced GenomicsG20RR030956 · NCRR · VANDERBILT UNIVERSITY · PI PIETENPOL, JENNIFER A · 2010 to 2010
$8.7M
Role of the Notch Pathway in Kidney InjuryR01DK076077 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI KATALIN SUSZTAK · 2007 to 2026
$8.0M
The Role of renal macrophages in recovery from renal injuryR01DK095785 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI RAYMOND C. HARRIS, Mingzhi Zhang · 2013 to 2026
$6.7M
Vanderbilt O'Brien Kidney Center - Core D - Clinical and Translational CoreP30DK114809 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI DE CAESTECKER, MARK P. · 2017 to 2021
$5.9M
Innovative therapeutic approaches to treat chronic kidney diseaseDP5OD033412 · OD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI TERKER, ANDREW S. · 2022 to 2025
$2.2M
BLRD VA I01 BX000320NCI NIH HHS P30 CA068485NCRR NIH HHS G20 RR030956NCRR NIH HHS UL1 RR024975NEI NIH HHS P30 EY008126NIDDK NIH HHS P30 DK114809NIDDK NIH HHS R01 DK051265NIDDK NIH HHS R01 DK062794NIDDK NIH HHS R01 DK076077NIDDK NIH HHS R01 DK095785NIH HHS DP5 OD033412
6 · The paper itself

Abstract

Fibrosis is the progressive accumulation of excess extracellular matrix and can cause organ failure. Fibrosis can affect nearly every organ including kidney and there is no specific treatment currently. Although Epidermal Growth Factor Receptor (EGFR) signaling pathway has been implicated in development of kidney fibrosis, underlying mechanisms by which EGFR itself mediates kidney fibrosis have not been elucidated. We find that EGFR expression increases in interstitial myofibroblasts in human and mouse fibrotic kidneys. Selective EGFR deletion in the fibroblast/pericyte population inhibits interstitial fibrosis in response to unilateral ureteral obstruction, ischemia or nephrotoxins. In vivo and in vitro studies and single-nucleus RNA sequencing analysis demonstrate that EGFR activation does not induce myofibroblast transformation but is necessary for the initial pericyte/fibroblast migration and proliferation prior to subsequent myofibroblast transformation by TGF-ß or other profibrotic factors. These findings may also provide insight into development of fibrosis in other organs and in other conditions.

Indexed as

Kidney DiseasesUreteral ObstructionAnimalsErbB ReceptorsFibrosisHumansKidneyMiceMyofibroblastsSignal TransductionEGFR protein, humanEGFR protein, mouseErbB Receptors

Identifiers

PMID37963889
PMCPMC10645887
OpenAlexW4388653865

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.