Evidence map›Paper›PMID 32911434›Full record

ArticleRedox biology2020

A functionally defined high-density NRF2 interactome reveals new conditional regulators of ARE transactivation.

Jonathan Poh, Amy H Ponsford, James Boyd, Jonathan Woodsmith, Ulrich Stelzl, Erich Wanker, Nicholas Harper, David MacEwan, Christopher M Sanderson

Open access · goldAbstract read
In one paragraph

Article in Redox biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 28% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Mitigation of Cardiovascular Disease and Toxicity through NRF2 Signalling.International journal of molecular sciences · 2023
    Review
  8. Review
  9. Review
  10. Review
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

9 authors at 3 institutions in 3 countries.

Jonathan PohInstitute of Translational Medicine, University of Liverpool, UK.
Amy H PonsfordInstitute of Translational Medicine, University of Liverpool, UK.
James BoydInstitute of Translational Medicine, University of Liverpool, UK.
Jonathan WoodsmithInstitute of Pharmaceutical Sciences, Department of Pharmaceutical Chemistry, University of Graz, Austria.
Ulrich StelzlInstitute of Pharmaceutical Sciences, Department of Pharmaceutical Chemistry, University of Graz, Austria.
Erich WankerMax-Delbrück Center for Molecular Medicine (MDC), Berlin-Buch, Germany.
Nicholas HarperInstitute of Translational Medicine, University of Liverpool, UK.
David MacEwanInstitute of Translational Medicine, University of Liverpool, UK.
Christopher M SandersonInstitute of Translational Medicine, University of Liverpool, UK. Electronic address: cmsand@liverpool.ac.uk.
University of Liverpool · GBUniversity of Graz · ATMax Delbrück Center · DE

Funding

Medical Research Council MR/K015931/1Wellcome TrustWellcome Trust 102172/Z/13/Z
6 · The paper itself

Abstract

NRF2 (NFE2L2) is a cytoprotective transcription factor associated with >60 human diseases, adverse drug reactions and therapeutic resistance. To provide insight into the complex regulation of NRF2 responses, 1962 predicted NRF2-partner interactions were systematically tested to generate an experimentally defined high-density human NRF2 interactome. Verification and conditional stratification of 46 new NRF2 partners was achieved by co-immunoprecipitation and the novel integration of quantitative data from dual luminescence-based co-immunoprecipitation (DULIP) assays and live-cell fluorescence cross-correlation spectroscopy (FCCS). The functional impact of new partners was then assessed in genetically edited loss-of-function (NRF2

Indexed as

Gene Expression RegulationNF-E2-Related Factor 2Cell LineHumansKelch-Like ECH-Associated Protein 1Transcriptional ActivationKelch-Like ECH-Associated Protein 1NFE2L2 protein, humanNF-E2-Related Factor 2Binary interactomeDual luminescence-based co-immunoprecipitation (DULIP)Fluorescence cross-correlation spectroscopy (FCCS)Human disease networkKEAP1NRF2/NFE2L2Protein interaction network (PIN)

Identifiers

PMID32911434
PMCPMC7490560
OpenAlexW3050682578

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.