Evidence map›Paper›PMID 30781847›Full record

ReviewMedicines (Basel, Switzerland)2019

Differential Methylation and Acetylation as the Epigenetic Basis of Resveratrol's Anticancer Activity.

Mohd Farhan, Mohammad Fahad Ullah, Mohd Faisal, Ammad Ahmad Farooqi, Uteuliyev Yerzhan Sabitaliyevich, Bernhard Biersack, Aamir Ahmad

Open access · goldAbstract readReview
In one paragraph

Review in Medicines (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

30 citing papers in PubMed, 58 citations in OpenAlex.

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  12. Jozimine AInternational journal of molecular sciences · 2024
    Article
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  17. The Aryl Hydrocarbon Receptor, Epigenetics and the Aging Process.The journal of nutrition, health & aging · 2023
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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

7 authors at 7 institutions in 6 countries.

Mohd FarhanCollege of Basic Sciences, King Faisal University, Hofuf 400-Al Ahsa-31982, Saudi Arabia. mfarhan@kfu.edu.sa.ORCID 0000-0002-1519-9644
Mohammad Fahad UllahDepartment of Medical Laboratory Technology, Faculty of Applied Medical Sciences, University of Tabuk, P.O. Box 741, Tabuk 71491, Saudi Arabia. m.ullah@ut.edu.sa.
Mohd FaisalDepartment of Psychiatry, University Hospital Limerick, Limerick V94 T9PX, Ireland. mohd.faisal@hse.ie.
Ammad Ahmad FarooqiInstitute of Biomedical and Genetic Engineering (IBGE), Islamabad 44000, Pakistan. ammadfarooqi@rlmclahore.com.
Uteuliyev Yerzhan SabitaliyevichDepartment of Postgraduate Education and Research, Kazakhstan Medical University KSPH, Almaty 050004, Kazakhstan. e.uteuliyev@ksph.kz.
Bernhard BiersackOrganic Chemistry Laboratory, Department of Chemistry, University of Bayreuth, Universitaetsstrasse 30, 95447 Bayreuth, Germany. bernhard.biersack@yahoo.com.
Aamir AhmadDepartment of Oncologic Sciences, Mitchell Cancer Institute, University of South Alabama, Mobile, AL 36604, USA. aahmad@health.southalabama.edu.ORCID 0000-0003-1784-5723
Institute of Biomedical and Genetic Engineering · PKKazakhstan Medical University · KZKing Faisal University · SAUniversity Hospital Limerick · IEUniversity of Bayreuth · DEUniversity of Tabuk · SAUSA Mitchell Cancer Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Numerous studies support the potent anticancer activity of resveratrol and its regulation of key oncogenic signaling pathways. Additionally, the activation of sirtuin 1, a deacetylase, by resveratrol has been known for many years, making resveratrol perhaps one of the earliest nutraceuticals with associated epigenetic activity. Such epigenetic regulation by resveratrol, and the mechanism thereof, has attracted much attention in the past decade. Focusing on methylation and acetylation, the two classical epigenetic regulations, we showcase the potential of resveratrol as an effective anticancer agent by virtue of its ability to induce differential epigenetic changes. We discuss the de-repression of tumor suppressors such as BRCA-1, nuclear factor erythroid 2-related factor 2 (NRF2) and Ras Associated Domain family-1α (RASSF-1α) by methylation, PAX1 by acetylation and the phosphatase and tensin homologue (PTEN) by both methylation and acetylation, in addition to the epigenetic regulation of oncogenic NF-κB and STAT3 signaling by resveratrol. Further, we evaluate the literature supporting the potentiation of HDAC inhibitors and the inhibition of DNMTs by resveratrol in different human cancers. This discussion underlines a robust epigenetic activity of resveratrol that warrants further evaluation, particularly in clinical settings.

Indexed as

acetylationepigeneticmethylationresveratrol

Identifiers

PMID30781847
PMCPMC6473688
OpenAlexW2915015695

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.