Evidence map›Paper›PMID 34650051›Full record

ArticleCell death & disease2021

The tyrosine-kinase inhibitor Nintedanib ameliorates autosomal-dominant polycystic kidney disease.

Abeda Jamadar, Sreenath M Suma, Sijo Mathew, Timothy A Fields, Darren P Wallace, James P Calvet, Reena Rao

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
5.0field-weighted citation impact, top 4% 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

29 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Macrophage-Fibroblast Crosstalk in Kidney Injury: A Narrative Review.International journal of molecular sciences · 2026
    Review
  3. Combination siRNA delivery as a therapeutic strategy for ADPKD.bioRxiv : the preprint server for biology · 2026
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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

7 authors at 2 institutions in 1 country.

Abeda JamadarThe Jared Grantham Kidney Institute, University of Kansas Medical Center, Kansas City, KS, USA.
Sreenath M SumaThe Jared Grantham Kidney Institute, University of Kansas Medical Center, Kansas City, KS, USA.
Sijo MathewDepartment of Pharmaceutical Sciences, School of Pharmacy, North Dakota State University, Fargo, ND, USA.
Timothy A FieldsDepartment of Pathology and Laboratory Medicine, University of Kansas Medical Center, Kansas City, KS, USA.
Darren P WallaceThe Jared Grantham Kidney Institute, University of Kansas Medical Center, Kansas City, KS, USA.
James P CalvetThe Jared Grantham Kidney Institute, University of Kansas Medical Center, Kansas City, KS, USA.ORCID 0000-0001-5928-9820
Reena RaoThe Jared Grantham Kidney Institute, University of Kansas Medical Center, Kansas City, KS, USA. rrao@kumc.edu.ORCID 0000-0003-0739-9344
University of Kansas Medical Center · USNorth Dakota State University · US

Funding

Mentoring CoreP20GM103418 · NIGMS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI Douglas E Wright · 2012 to 2026
$63.0M
Polycystin Function Resource Development CoreU54DK126126 · NIDDK · UNIVERSITY OF KANSAS MEDICAL CENTER · PI DARREN P. WALLACE · 2020 to 2026
$5.8M
Center for Polycystic Kidney Disease Research at YaleP30DK090744 · NIDDK · YALE UNIVERSITY · PI CAPLAN, MICHAEL J. · 2010 to 2014
$5.6M
Regulation of Renal Response to Vasopressin by Glycogen SynthaseR01DK083525 · NIDDK · UNIVERSITY OF KANSAS MEDICAL CENTER · PI RAO, REENA · 2011 to 2020
$2.5M
Spinning-Disk Confocal Microscope for Wide-Field, Super-Resolution, and Live-Cell ImagingS10OD032207 · OD · UNIVERSITY OF KANSAS MEDICAL CENTER · PI SMITH, PETER G · 2022 to 2022
$600k
NIDDK NIH HHS P30 DK090744NIDDK NIH HHS R01 DK083525NIDDK NIH HHS U54 DK126126NIGMS NIH HHS P20 GM103418NIH HHS S10 OD032207
6 · The paper itself

Abstract

Autosomal-dominant polycystic kidney disease (ADPKD) is the most common inherited kidney disease and is characterized by progressive growth of fluid-filled cysts. Growth factors binding to receptor tyrosine kinases (RTKs) stimulate cell proliferation and cyst growth in PKD. Nintedanib, a triple RTK inhibitor, targets the vascular endothelial growth-factor receptor (VEGFR), platelet-derived growth-factor receptor (PDGFR), and fibroblast growth-factor receptor (FGFR), and is an approved drug for the treatment of non-small-cell lung carcinoma and idiopathic lung fibrosis. To determine if RTK inhibition using nintedanib can slow ADPKD progression, we tested its effect on human ADPKD renal cyst epithelial cells and myofibroblasts in vitro, and on Pkd1

Indexed as

AnimalsCell MovementCell ProliferationCell SurvivalEpithelial CellsHumansIndolesKidneyMiceMice, KnockoutMyofibroblastsPolycystic Kidney, Autosomal DominantProtein Kinase InhibitorsReceptors, Cell SurfaceSignal TransductionIndolesnintedanibPkhd1 protein, mouseProtein Kinase InhibitorsReceptors, Cell Surface

Identifiers

PMID34650051
PMCPMC8517027
OpenAlexW3207767923

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.