Evidence map›Paper›PMID 34716241›Full record

ArticleJournal of the American Society of Nephrology : JASN2021

Ferroptosis Promotes Cyst Growth in Autosomal Dominant Polycystic Kidney Disease Mouse Models.

Xiaoqin Zhang, Linda Xiaoyan Li, Hao Ding, Vicente E Torres, Chen Yu, Xiaogang Li

Open access · greenAbstract read
In one paragraph

Article in Journal of the American Society of Nephrology : JASN, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
9.4field-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

52 citing papers in PubMed, 76 citations in OpenAlex.

  1. Ferroptosis in kidney disease.Nature reviews. Nephrology · 2026
    Review
  2. Ferroptosis as a target mechanism in heart and kidney disease.The Journal of clinical investigation · 2026
    Review
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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 3 institutions in 2 countries.

Xiaoqin ZhangDepartment of Internal Medicine, Mayo Clinic, Rochester, Minnesota.
Linda Xiaoyan LiDepartment of Internal Medicine, Mayo Clinic, Rochester, Minnesota.
Hao DingDepartment of Internal Medicine, Mayo Clinic, Rochester, Minnesota.
Vicente E TorresDepartment of Internal Medicine, Mayo Clinic, Rochester, Minnesota.
Chen YuDepartment of Nephrology, Tongji Hospital, School of Medicine, Tongji University, Shanghai, China.
Xiaogang LiDepartment of Internal Medicine, Mayo Clinic, Rochester, Minnesota.
Mayo Clinic · USTongji Hospital · CNTongji University · CN

Funding

Renal Physiology and Phenotyping CoreP30DK079310 · NIDDK · YALE UNIVERSITY · PI SOMLO, STEFAN · 2008 to 2022
$16.8M
Pilot and FeasibilityP30DK090728 · NIDDK · MAYO CLINIC ROCHESTER · PI TORRES, VICENTE E · 2010 to 2019
$11.8M
Pilot and Feasibility CoreP30DK106912 · NIDDK · UNIVERSITY OF KANSAS MEDICAL CENTER · PI CALVET, JAMES P · 2015 to 2019
$5.5M
RENIN ANGIOTENSIN SYSTEM IN THE PATHOGENESIS OF ADPKDR01DK044863 · NIDDK · MAYO CLINIC ROCHESTER · PI TORRES, VICENTE E · 1991 to 2019
$4.5M
The crosstalk of DNA and lysine methyltransferases in ADPKD.R01DK126662 · NIDDK · MAYO CLINIC ROCHESTER · PI Xiaogang Li · 2020 to 2026
$3.0M
ADPKD: Understanding mechanisms, Discovering treatments.R01DK084097 · NIDDK · UNIVERSITY OF KANSAS MEDICAL CENTER · PI LI, XIAOGANG · 2010 to 2018
$2.3M
ADPKD: Understanding immunosuppression mechanisms and discovering treatmentR01DK129241 · NIDDK · MAYO CLINIC ROCHESTER · PI LI, XIAOGANG · 2021 to 2024
$1.8M
NIDDK NIH HHS P30 DK079310NIDDK NIH HHS P30 DK090728NIDDK NIH HHS P30 DK106912NIDDK NIH HHS R01 DK044863NIDDK NIH HHS R01 DK084097NIDDK NIH HHS R01 DK126662NIDDK NIH HHS R01 DK129241
6 · The paper itself

Abstract

backgroundAutosomal dominant polycystic kidney disease (ADPKD), the most common inherited kidney disease, is regulated by different forms of cell death, including apoptosis and autophagy. However, the role in ADPKD of ferroptosis, a recently discovered form of cell death mediated by iron and lipid metabolism, remains elusive.

methodsTo determine a pathophysiologic role of ferroptosis in ADPKD, we investigated whether the absence of

resultsWe found that kidney cells and tissues lacking

conclusionThese findings indicate that ferroptosis contributes to ADPKD progression and management of ferroptosis may be a novel strategy for ADPKD treatment.

Indexed as

FerroptosisAnimalsCell CycleCells, CulturedCyclohexylaminesDisease Models, AnimalDisease ProgressionEpithelial CellsFemaleGene Expression RegulationHumansIronLipid PeroxidationMaleMiceMice, Inbred BALB CCyclohexylamineserastinferrostatin-1IronPhenylenediaminesPiperazinesTRPP Cation Channels4HNEcell proliferationferroptosisiron metabolismlipid peroxidation

Identifiers

PMID34716241
PMCPMC8806097
OpenAlexW3208250521

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.