Evidence map›Paper›PMID 36296565›Full record

ArticleMolecules (Basel, Switzerland)2022

Resveratrol Analogues as Selective Estrogen Signaling Pathway Modulators: Structure-Activity Relationship.

Paulina Kobylka, Malgorzata Kucinska, Jacek Kujawski, Dawid Lazewski, Marcin Wierzchowski, Marek Murias

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

22 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
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  4. Review
  5. Bromo Analogues of Active 3,4,5,4'-Tetramethoxy-Molecules (Basel, Switzerland) · 2025
    Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Review
  11. Heliyon · 2024
    Article
  12. The Role of Estrogen across Multiple Disease Mechanisms.Current issues in molecular biology · 2024
    Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Review
  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

6 authors at 1 institution in 1 country.

Paulina KobylkaDepartment of Toxicology, Poznan University of Medical Sciences, 60-631 Poznan, Poland.
Malgorzata KucinskaDepartment of Toxicology, Poznan University of Medical Sciences, 60-631 Poznan, Poland.ORCID 0000-0002-3606-3623
Jacek KujawskiChair and Department of Organic Chemistry, Poznan University of Medical Sciences, 60-780 Poznan, Poland.ORCID 0000-0001-6279-4887
Dawid LazewskiChair and Department of Chemical Technology of Drugs, Poznan University of Medical Sciences, 60-780 Poznan, Poland.ORCID 0000-0002-9832-5094
Marcin WierzchowskiChair and Department of Chemical Technology of Drugs, Poznan University of Medical Sciences, 60-780 Poznan, Poland.
Marek MuriasDepartment of Toxicology, Poznan University of Medical Sciences, 60-631 Poznan, Poland.ORCID 0000-0002-2903-4912
Poznan University of Medical Sciences · PL

Funding

Poznan University of Medical Sciences Doctoral School 4707
6 · The paper itself

Abstract

Resveratrol is a plant-derived phytoalexin found in grapes, red wine and many other plants used in Asian folk medicine. It is extensively studied for pleiotropic biological activity. The most crucial are anticancer and chemopreventive properties. Resveratrol has also been reported to be an antioxidant and phytoestrogen. The phytoestrogenic activity of resveratrol was assayed in different in vitro and in vivo models. Although these works brought some, on the first look, conflicting results, it is commonly accepted that resveratrol interacts with estrogen receptors and functions as a mixed agonist/antagonist. It is widely accepted that the hydroxyl groups are crucial for resveratrol's cytotoxic and antioxidative activity and are responsible for binding estrogen receptors. In this work, we assayed 11 resveratrol analogues, seven barring methoxy groups and six hydroxylated analogues in different combinations at positions 3, 4, 5 and 3',4',5'. For this purpose, recombined estrogen receptors and estrogen-dependent MCF-7 and Ishikawa cells were used. Our study was supported by in silico docking studies. We have shown that, resveratrol and 3,4,4'5'-tetrahydroxystilbene, 3,3',4,5,5'-pentahydroxystilbene and 3,3',4,4',5,5'-hexahydroxystilbene may act as selective estrogen receptor modulators.

Indexed as

Receptors, EstrogenStilbenesAntioxidantsEstrogensPhytoestrogensResveratrolSelective Estrogen Receptor ModulatorsSignal TransductionStructure-Activity RelationshipAntioxidantsEstrogensPhytoestrogensReceptors, EstrogenResveratrolSelective Estrogen Receptor ModulatorsStilbenesestrogen receptorresveratrolresveratrol analogues

Identifiers

PMID36296565
PMCPMC9608462
OpenAlexW4306673007

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.