Evidence map›Paper›PMID 28585088›Full record

ArticleMolecular and cellular biochemistry2018

Allyl isothiocyanate, a potent chemopreventive agent targets AhR/Nrf2 signaling pathway in chemically induced mammary carcinogenesis.

Thangarasu Rajakumar, Pachaiappan Pugalendhi, Subbaiyan Thilagavathi, Dhanabalan Ananthakrishnan, Krishnaswamy Gunasekaran

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In one paragraph

Article in Molecular and cellular biochemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

13 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Isothiocyanate-Rich Extracts from Cauliflower (International journal of environmental research and public health · 2022
    Article
  9. Review
  10. Review
  11. International journal of molecular sciences · 2020
    Review
  12. Potential Applications of NRF2 Modulators in Cancer Therapy.Antioxidants (Basel, Switzerland) · 2020
    Review
  13. 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

5 authors at 2 institutions in 1 country.

Thangarasu RajakumarDepartment of Biochemistry and Biotechnology, Faculty of Science, Annamalai University, Annamalainagar, Chidambaram, Tamil Nadu, 608 002, India.
Pachaiappan PugalendhiDepartment of Biochemistry and Biotechnology, Faculty of Science, Annamalai University, Annamalainagar, Chidambaram, Tamil Nadu, 608 002, India. pugalau@gmail.com.
Subbaiyan ThilagavathiDepartment of Biochemistry and Biotechnology, Faculty of Science, Annamalai University, Annamalainagar, Chidambaram, Tamil Nadu, 608 002, India.
Dhanabalan AnanthakrishnanCenter of Advanced Studies in Crystallography and Biophysics, University of Madras, Guindy Campus, Chennai, Tamil Nadu, 600 025, India.
Krishnaswamy GunasekaranCenter of Advanced Studies in Crystallography and Biophysics, University of Madras, Guindy Campus, Chennai, Tamil Nadu, 600 025, India.
Annamalai University · INUniversity of Madras · IN

Funding

Indian Council of Medical Research (Grant No. 3/2/2/189/2013/NCD-III (OPA-27129))
6 · The paper itself

Abstract

In the present study, we investigated the effect of allyl isothiocyanate (AITC) on liver detoxification signaling pathway in 7,12-dimethylbenz(a)anthracene (DMBA)-induced mammary carcinogenesis. Mammary tumor was induced by a single dose of DMBA (25 mg/rat) injected subcutaneously near the mammary gland in Sprague-Dawley rats. DMBA-alone-treated rats show an increased synthesis of phase I detoxification enzymes, lipid peroxidative markers, liver marker enzymes, and lipid profiles whereas, depletion of phase II detoxification enzymes and antioxidants in rat liver tissues. Oral administration of AITC restored the levels of biochemical markers in DMBA-treated rats. Furthermore, histopathological results also confirmed that AITC protects DMBA-mediated hepatocellular damage. We also observed that AITC treatment significantly downregulates AhR and upregulates the expression of Nrf2 in DMBA-treated rats. The binding efficacy of AITC with AhR and Nrf2 analysis by molecular docking studies reveals that AITC has strong interaction with AhR and Nrf2 proteins through hydrogen and hydrophobic interactions. Thus, AITC prevents DMBA-induced mammary carcinogenesis via inhibition of phase I and induction of phase II detoxification enzymes by modulating AhR/Nrf2 signaling pathway.

Indexed as

Cell Transformation, NeoplasticMammary Neoplasms, Experimental9,10-Dimethyl-1,2-benzanthraceneAnimalsBasic Helix-Loop-Helix ProteinsFemaleIsothiocyanatesNeoplasm ProteinsNF-E2-Related Factor 2RatsRats, Sprague-DawleyReceptors, Aryl HydrocarbonSignal Transduction9,10-Dimethyl-1,2-benzanthraceneAhr protein, ratallyl isothiocyanateBasic Helix-Loop-Helix ProteinsIsothiocyanatesNeoplasm ProteinsNfe2l2 protein, ratNF-E2-Related Factor 2Receptors, Aryl Hydrocarbon7,12-Dimethylbenz(a)anthraceneAllyl isothiocyanateAryl hydrocarbon receptorDetoxification enzymesMammary carcinogenesisNuclear factor erythroid 2-related factor 2

Identifiers

PMID28585088
OpenAlexW2621424694

What OpenQuestion holds

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Registered trials

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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.