Evidence map›Paper›PMID 31372933›Full record

ReviewArchives of pharmacal research2020

Filtering through the role of NRF2 in kidney disease.

Cody J Schmidlin, Matthew B Dodson, Donna D Zhang

Open access · greenAbstract readReview
In one paragraph

Review in Archives of pharmacal research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 14% 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, 1 synthesis or guideline pooled it, 34 citations in OpenAlex.

  1. Pooled it
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  15. Tackling of Renal Carcinogenesis in Wistar Rats byOxidative medicine and cellular longevity · 2021
    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

3 authors at 1 institution in 1 country.

Cody J SchmidlinDepartment of Pharmacology and Toxicology, University of Arizona, Tucson, AZ, USA.
Matthew B DodsonDepartment of Pharmacology and Toxicology, University of Arizona, Tucson, AZ, USA.
Donna D ZhangDepartment of Pharmacology and Toxicology, University of Arizona, Tucson, AZ, USA. dzhang@pharmacy.arizona.edu.
University of Arizona · US

Funding

TRANSPORT OF TRACE METALS IN A POLLUTED AQUIFERP42ES004940 · NIEHS · UNIVERSITY OF ARIZONA · PI Xinxin Ding · 1990 to 2026
$68.1M
SOUTHWEST ENVIRONMENTAL HEALTH SCIENCES CENTERP30ES006694 · NIEHS · UNIVERSITY OF ARIZONA · PI DEAN BILLHEIMER · 1994 to 2026
$36.7M
Training in Environmental Toxicology of Human DiseaseT32ES007091 · NIEHS · UNIVERSITY OF ARIZONA · PI Nathan J Cherrington · 1985 to 2026
$10.7M
NRF Transcription Factors in Environmental Stress and Disease InterventionR35ES031575 · NIEHS · UNIVERSITY OF FLORIDA · PI Donna D Zhang · 2020 to 2026
$7.1M
Arsenic, Nrf2 and Autophagy Dysfunction in Type II DiabetesR01DK109555 · NIDDK · UNIVERSITY OF ARIZONA · PI ZHANG, DONNA D · 2016 to 2019
$1.4M
Nrf2, autophagy, and arsenic carcinogenesisR01ES026845 · NIEHS · UNIVERSITY OF ARIZONA · PI ZHANG, DONNA D · 2016 to 2019
$1.4M
NIDDK NIH HHS DK109555NIDDK NIH HHS R01 DK109555NIEHS NIH HHS ES004940NIEHS NIH HHS ES006694NIEHS NIH HHS ES026845NIEHS NIH HHS P30 ES006694NIEHS NIH HHS P42 ES004940NIEHS NIH HHS R01 ES026845NIEHS NIH HHS R35 ES031575NIEHS NIH HHS T32 ES007091
6 · The paper itself

Abstract

Kidney disease affects ~ 10% of the population worldwide, resulting in millions of deaths each year. Mechanistically, oxidative stress is a major driver of various kidney diseases, and promotes the progression from acute to chronic injury, as well as renal cancer development. NRF2, the master regulator of redox balance, has been shown to protect against kidney disease through its negation of reactive oxygen species (ROS). However, many kidney diseases exhibit high levels of ROS as a result of decreased NRF2 protein levels and transcriptional activity. Many studies have tested the strategy of using NRF2 inducing compounds to alleviate ROS to prevent or slow down the progression of kidney diseases. Oppositely, in specific subsets of renal cancer, NRF2 is constitutively activated and contributes to tumor burden and overall poor prognosis; therefore, there has been a recent interest in studies investigating the benefits of NRF2 inhibition. In this review, we summarize recent literature investigating the role of NRF2 and oxidative stress in various kidney diseases, and how pharmacological modification of NRF2 signaling could play a protective role.

Indexed as

AnimalsHumansKidney DiseasesNF-E2-Related Factor 2Oxidative StressProtective AgentsReactive Oxygen SpeciesSignal TransductionNF-E2-Related Factor 2Protective AgentsReactive Oxygen SpeciesHypertensionKEAP1Kidney diseaseNRF2Oxidative stressRenal cell carcinoma

Identifiers

PMID31372933
PMCPMC6994339
OpenAlexW2964506938

What OpenQuestion holds

Textmetadata
LicenceTDM
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.