Evidence map›Paper›PMID 34521933›Full record

Trial reportScientific reports2021

Impact of isoflavone genistein on psoriasis in in vivo and in vitro investigations.

Katarzyna Bocheńska, Marta Moskot, Elwira Smolińska-Fijołek, Joanna Jakóbkiewicz-Banecka, Aneta Szczerkowska-Dobosz, Bartosz Słomiński, Magdalena Gabig-Cimińska

Open access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

14 citing papers in PubMed, 22 citations in OpenAlex.

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  14. Regulatory Roles of Estrogens in Psoriasis.Journal of clinical medicine · 2022
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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 2 institutions in 1 country.

Katarzyna BocheńskaDepartment of Medical Biology and Genetics, University of Gdańsk, Wita Stwosza 59, 80-308, Gdańsk, Poland.
Marta MoskotDepartment of Medical Biology and Genetics, University of Gdańsk, Wita Stwosza 59, 80-308, Gdańsk, Poland.
Elwira Smolińska-FijołekDepartment of Medical Biology and Genetics, University of Gdańsk, Wita Stwosza 59, 80-308, Gdańsk, Poland.
Joanna Jakóbkiewicz-BaneckaDepartment of Medical Biology and Genetics, University of Gdańsk, Wita Stwosza 59, 80-308, Gdańsk, Poland.
Aneta Szczerkowska-DoboszDepartment of Dermatology, Venereology and Allergology, Medical University of Gdańsk, Mariana Smoluchowskiego 17, 80-214, Gdańsk, Poland.
Bartosz SłomińskiDepartment of Immunology, Faculty of Medicine, Medical University of Gdańsk, Dębinki 1, 80-211, Gdańsk, Poland.
Magdalena Gabig-CimińskaDepartment of Medical Biology and Genetics, University of Gdańsk, Wita Stwosza 59, 80-308, Gdańsk, Poland. magdalena.gabig-ciminska@ug.edu.pl.
Gdańsk Medical University · PLInstitute of Biochemistry and Biophysics, Polish Academy of Sciences · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genistein is applied worldwide as an alternative medicament for psoriasis (Ps) because of its anti-inflammatory activity and perceived beneficial impact on the skin. Hereby, we report our in vivo and in vitro investigations to supplement scientific research in this area. The reduction of clinical and biochemical scores in mild to moderate Ps patients taking genistein, its safety, good tolerability with no serious adverse events or discontinuations of treatment, no dose-limiting toxicities, negligible changes in pharmacodynamic parameters and remarkable serum interleukin level alterations were documented in this study. A certain regression of the Ps phenotype was visible, based on photo-documented Ps lesion evaluation. Through in vitro experiments, we found that genistein reduced IL-17A and TNF-α induced MAPK, NF-κB, and PI3K activation in normal human epidermal keratinocytes. Moreover, at the mRNA level of genes associated with the early inflammatory response characteristic for Ps (CAMP, CCL20, DEFB4A, PIK3CA, S100A7, and S100A9) and key cellular signalling (MTORC1 and TFEB), we showed that this isoflavone attenuated the increased response of IL-17A- and TNF-α-related pathways. This allows us to conclude that genistein is a good candidate for Ps treatment, being attractive for co-pharmacotherapy with other drugs.

Indexed as

AdultAnti-Inflammatory AgentsCell LineCytokinesFemaleFluorescent Antibody TechniqueGenisteinHumansKeratinocytesMaleMiddle AgedPsoriasisReal-Time Polymerase Chain ReactionAnti-Inflammatory AgentsCytokinesGenistein

Identifiers

PMID34521933
PMCPMC8440511
OpenAlexW3200186047

What OpenQuestion holds

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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.