Evidence map›Paper›PMID 33963962›Full record

ArticleInvestigational new drugs2021

Benzyl and phenethyl isothiocyanates as promising epigenetic drug compounds by modulating histone acetylation and methylation marks in malignant melanoma.

Melina Mitsiogianni, Ioannis Anestopoulos, Sotiris Kyriakou, Dimitrios T Trafalis, Rodrigo Franco, Aglaia Pappa, Mihalis I Panayiotidis

Abstract read
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In one paragraph

Article in Investigational new drugs, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

12 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Anticarcinogenic Effects of Isothiocyanates on Hepatocellular Carcinoma.International journal of molecular sciences · 2022
    Review
  10. Article
  11. Article
  12. 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

7 authors at 6 institutions in 4 countries.

Melina MitsiogianniDepartment of Applied Sciences, Northumbria University, Newcastle Upon Tyne, UK.
Ioannis AnestopoulosDepartment of Cancer Genetics, Therapeutics & Ultrastructural Pathology, The Cyprus Institute of Neurology & Genetics, Nicosia, Cyprus.
Sotiris KyriakouDepartment of Cancer Genetics, Therapeutics & Ultrastructural Pathology, The Cyprus Institute of Neurology & Genetics, Nicosia, Cyprus.
Dimitrios T TrafalisLaboratory of Pharmacology, Clinical Pharmacology Unit, Medical School, National & Kapodistrian University of Athens, Athens, Greece.
Rodrigo FrancoRedox Biology Centre, University of Nebraska-Lincoln, Lincoln, Nebraska, USA.
Aglaia PappaDepartment of Molecular Biology & Genetics, Democritus University of Thrace, Alexandroupolis, Greece.
Mihalis I PanayiotidisDepartment of Applied Sciences, Northumbria University, Newcastle Upon Tyne, UK. mihalisp@cing.ac.cy.ORCID 0000-0002-1450-3552
Cyprus Institute of Neurology and Genetics · CYCyprus Institute of Marketing · CYDemocritus University of Thrace · GRNational and Kapodistrian University of Athens · GRNorthumbria University · GBUniversity of Nebraska–Lincoln · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Melanoma is an aggressive skin cancer with increasing incidence rates globally. On the other hand, isothiocyanates are derived from cruciferous vegetables and are known to exert a wide range of anti-cancer activities including, among others, their ability to interact with the epigenome in order to supress cancer progression. The aim of this study was to determine the role of phenethyl and benzyl isothiocyanates in modulating histone acetylation and methylation as a potential epigenetic therapeutic strategy in an in vitro model of malignant melanoma. We report that both isothiocyanates induced cytotoxicity and influenced acetylation and methylation status of specific lysine residues on histones H3 and H4 by modulating the expression of various histone acetyltransferases, deacetylases and methyltransferases in malignant melanoma cells. Our data highlight novel insights on the interaction of isothiocyanates with components of the histone regulatory machinery in order to exert their anti-cancer action in malignant melanoma.

Indexed as

AcetylationCell Line, TumorCell SurvivalEpigenesis, GeneticHistonesHumansIsothiocyanatesMelanomaMethylationSkin Neoplasmsbenzyl isothiocyanateHistonesIsothiocyanatesphenethyl isothiocyanateepigeneticsisothiocyanateslysine acetylationlysine methylation, cancer therapeuticsmelanoma

Identifiers

PMID33963962
OpenAlexW3158945631

What Socratic holds

Textmetadata
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 Socratic graph.