Evidence map›Paper›PMID 27794453›Full record

ReviewFree radical biology & medicine2017

Regulatory roles of glutathione-S-transferases and 4-hydroxynonenal in stress-mediated signaling and toxicity.

Yogesh C Awasthi, Kota V Ramana, Pankaj Chaudhary, Satish K Srivastava, Sanjay Awasthi

Open access · greenAbstract readReview
In one paragraph

Review in Free radical biology & medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

34 citing papers in PubMed, 66 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. 4-Hydroxynonenal, a Potential Biomarker for Lung Inflammatory Diseases.International journal of molecular sciences · 2026
    Review
  5. Oxeiptosis - potential in cancer treatment?Expert reviews in molecular medicine · 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

5 authors at 3 institutions in 1 country.

Yogesh C AwasthiDepartment of Biochemistry and Molecular Biology, University of Texas Medical Branch, Galveston, TX 77555, USA. Electronic address: Yogesh.Awasthi@live.unthsc.edu.
Kota V RamanaDepartment of Biochemistry and Molecular Biology, University of Texas Medical Branch, Galveston, TX 77555, USA. Electronic address: kvramana@utmb.edu.
Pankaj ChaudharyDepartment of Molecular and Medical Genetics, University of North Texas Health Science Center, Fort worth, TX 76107, USA.
Satish K SrivastavaDepartment of Biochemistry and Molecular Biology, University of Texas Medical Branch, Galveston, TX 77555, USA.
Sanjay AwasthiDepartment of Internal Medicine-Oncology, Texas Tech University Health Sciences Center, Lubbock, TX 79430, USA.
The University of Texas Medical Branch at Galveston · USTexas Tech University Health Sciences Center · USUniversity of North Texas Health Science Center · US

Funding

Chemoprevention of Colorectal Cancer by Aldose Reductase InhibitionR01CA129383 · NCI · UNIVERSITY OF TEXAS MED BR GALVESTON · PI RAMANA, KOTA VENKATA · 2008 to 2017
$3.1M
Role of Aldose Reductase in Diabetic ComplicationsR01DK104786 · NIDDK · UNIVERSITY OF TEXAS MED BR GALVESTON · PI RAMANA, KOTA VENKATA · 2015 to 2019
$2.2M
ALDOSE REDUCTASE AND DIABETIC COMPLICATIONSR01DK036118 · NIDDK · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI SRIVASTAVA, SATISH K · 1987 to 2002
$626k
NCI NIH HHS R01 CA129383NIDDK NIH HHS R01 DK036118NIDDK NIH HHS R01 DK104786
6 · The paper itself

Abstract

Glutathione-S-Transferases (GSTs) have primarily been thought to be xenobiotic metabolizing enzymes that protect cells from toxic drugs and environmental electrophiles. However, in last three decades, these enzymes have emerged as the regulators of oxidative stress-induced signaling and toxicity. 4-Hydroxy-trans 2-nonenal (HNE) an end-product of lipid peroxidation, has been shown to be a major determinant of oxidative stress-induced signaling and toxicity. HNE is involved in signaling pathways, including apoptosis, proliferation, modulation of gene expression, activation of transcription factors/repressors, cell cycle arrest, and differentiation. In this article, available evidence for a major role of GSTs in the regulation of HNE-mediated cell signaling processes through modulation of the intracellular levels of HNE is discussed.

Indexed as

Adaptor Proteins, Signal TransducingAldehydesAnimalsApoptosisCell Cycle ProteinsCell Line, TumorCell ProliferationCell SurvivalCo-Repressor ProteinsGene Expression RegulationGlutathione TransferaseHeat Shock Transcription FactorsHumansLipid PeroxidationMolecular ChaperonesNuclear Proteins4-hydroxy-2-nonenalAdaptor Proteins, Signal TransducingAldehydesCell Cycle ProteinsCo-Repressor ProteinsDAXX protein, humanGlutathione TransferaseHeat Shock Transcription FactorsHSF1 protein, humanMolecular ChaperonesNuclear Proteins4-hydroxynonenalCell cycleCell signalingGlutathione-S-transferasesOxidative stress

Identifiers

PMID27794453
PMCPMC5643026
OpenAlexW2542760843

What OpenQuestion holds

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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.