Evidence map›Paper›PMID 32649885›Full record

ReviewCancer cell2020

Oxidative Stress in Cancer.

John D Hayes, Albena T Dinkova-Kostova, Kenneth D Tew

Open access · bronzeAbstract readReview
In one paragraph

Review in Cancer cell, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1,321 papers.

0numbers the graph read from it
0cells of the map it votes in
1,321citing papers in PubMed
95.4field-weighted citation impact, top 1% 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

1,321 citing papers in PubMed, 2,420 citations in OpenAlex.

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  6. Imaging xCT with Immuno-PET in Therapy-Resistant Non-Small Cell Lung Cancer.Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2026
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1,261 more citing papers are in PubMed but not listed here.

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 2 institutions in 2 countries.

John D HayesDivision of Cellular Medicine, Jacqui Wood Cancer Centre, Ninewells Hospital and Medical School, University of Dundee, Dundee DD1 9SY, UK, Scotland. Electronic address: j.d.hayes@dundee.ac.uk.
Albena T Dinkova-KostovaDivision of Cellular Medicine, Jacqui Wood Cancer Centre, Ninewells Hospital and Medical School, University of Dundee, Dundee DD1 9SY, UK, Scotland; Department of Pharmacology and Molecular Sciences and Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Kenneth D TewDepartment of Cell and Molecular Pharmacology, Medical University of South Carolina, Charleston, SC 29425, USA.
University of Dundee · GBMedical University of South Carolina · US

Funding

SOUTH CAROLINA COBRE IN OXIDANTS, REDOX BALANCE AND STRESS SIGNALINGP20GM103542 · NIGMS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI LEMASTERS, JOHN J · 2012 to 2020
$20.2M
MUSC FACIL EXPANSION &RENOV: SLE C06RR015455 · NCRR · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI CROUCH, ROSALIE K · 2002 to 2002
$2.0M
Cancer Research UK 18644Cancer Research UK C20953/A18644Medical Research Council MR/N009851/1Medical Research Council MR/T014644/1NCRR NIH HHS C06 RR015455NIGMS NIH HHS P20 GM103542
6 · The paper itself

Abstract

Contingent upon concentration, reactive oxygen species (ROS) influence cancer evolution in apparently contradictory ways, either initiating/stimulating tumorigenesis and supporting transformation/proliferation of cancer cells or causing cell death. To accommodate high ROS levels, tumor cells modify sulfur-based metabolism, NADPH generation, and the activity of antioxidant transcription factors. During initiation, genetic changes enable cell survival under high ROS levels by activating antioxidant transcription factors or increasing NADPH via the pentose phosphate pathway (PPP). During progression and metastasis, tumor cells adapt to oxidative stress by increasing NADPH in various ways, including activation of AMPK, the PPP, and reductive glutamine and folate metabolism.

Indexed as

Oxidative StressAnimalsAntioxidantsApoptosisEnergy MetabolismGlucoseHumansNADPNeoplasmsReactive Oxygen SpeciesAntioxidantsGlucoseNADPReactive Oxygen SpeciesadaptationantioxidantAP-1BACH1dormant cancer cellfolate metabolismFOXOglutathioneHIF-1alphaHSF1initiationmetastasisNADPH generationNF-κBNRF2oxidative stresspentose phosphate pathwayPGC-1alphaprogressionreactive oxygen speciesrecurrent diseaseredox signalingreductive glutamine metabolismthioredoxinTP53tumorigenesis

Identifiers

PMID32649885
PMCPMC7439808
OpenAlexW3041426930

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.