Evidence map›Paper›PMID 29710398›Full record

ReviewMolecular nutrition & food research2018

Phenethyl Isothiocyanate, a Dual Activator of Transcription Factors NRF2 and HSF1.

Sharadha Dayalan Naidu, Takafumi Suzuki, Masayuki Yamamoto, Jed W Fahey, Albena T Dinkova-Kostova

Open access · hybridAbstract readReview
In one paragraph

Review in Molecular nutrition & food research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 11% 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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 51 citations in OpenAlex.

  1. Pooled it
  2. Effects of 2-Phenethyl Isothiocyanate on Metabolism of 1,3-Butadiene in Smokers.Cancer prevention research (Philadelphia, Pa.) · 2020
    Trial
  3. Trial
  4. Article
  5. Article
  6. Article
  7. The Anti-AGEing and RAGEing Potential of Isothiocyanates.Molecules (Basel, Switzerland) · 2024
    Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article
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 2 institutions in 3 countries.

Sharadha Dayalan NaiduCullman Chemoprotection Center, Johns Hopkins University, Baltimore, MD, 21205, USA.ORCID 0000-0002-7692-5611
Takafumi SuzukiDepartment of Medical Biochemistry, Tohoku University Graduate School of Medicine, Sendai, 980-8575, Japan.
Masayuki YamamotoDepartment of Medical Biochemistry, Tohoku University Graduate School of Medicine, Sendai, 980-8575, Japan.
Jed W FaheyCullman Chemoprotection Center, Johns Hopkins University, Baltimore, MD, 21205, USA.
Albena T Dinkova-KostovaCullman Chemoprotection Center, Johns Hopkins University, Baltimore, MD, 21205, USA.ORCID 0000-0003-0316-9859
Johns Hopkins University · USTohoku University · JP

Funding

Cancer Research UK 18644Cancer Research UK C20953/A18644
6 · The paper itself

Abstract

Cruciferous vegetables are rich sources of glucosinolates which are the biogenic precursor molecules of isothiocyanates (ITCs). The relationship between the consumption of cruciferous vegetables and chemoprotection has been widely documented in epidemiological studies. Phenethyl isothiocyanate (PEITC) occurs as its glucosinolate precursor gluconasturtiin in the cruciferous vegetable watercress (Nasturtium officinale). PEITC has multiple biological effects, including activation of cytoprotective pathways, such as those mediated by the transcription factor nuclear factor erythroid 2 p45-related factor 2 (NRF2) and the transcription factor heat shock factor 1 (HSF1), and can cause changes in the epigenome. However, at high concentrations, PEITC leads to accumulation of reactive oxygen species and cytoskeletal changes, resulting in cytotoxicity. Underlying these activities is the sulfhydryl reactivity of PEITC with cysteine residues in its protein targets. This chemical reactivity highlights the critical importance of the dose of PEITC for achieving on-target selectivity, which should be carefully considered in the design of future clinical trials.

Indexed as

AnimalsCell Line, TumorCytoprotectionEpigenesis, GeneticGene Expression RegulationGlucosinolatesHeat Shock Transcription FactorsHumansIsothiocyanatesNasturtiumNF-E2-Related Factor 2NF-E2 Transcription Factor, p45 SubunitReactive Oxygen SpeciesVegetablesgluconasturtiinGlucosinolatesHeat Shock Transcription FactorsIsothiocyanatesNF-E2-Related Factor 2NF-E2 Transcription Factor, p45 Subunitphenethyl isothiocyanateReactive Oxygen SpeciesHSF1HSP90KEAP1NRF2PEITC

Identifiers

PMID29710398
PMCPMC6175120
OpenAlexW2801413673

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.