Evidence map›Paper›PMID 29444128›Full record

ArticlePloS one2018

Molecular action of isoflavone genistein in the human epithelial cell line HaCaT.

Elwira Smolińska, Marta Moskot, Joanna Jakóbkiewicz-Banecka, Grzegorz Węgrzyn, Bogdan Banecki, Aneta Szczerkowska-Dobosz, Dorota Purzycka-Bohdan, Magdalena Gabig-Cimińska

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

24 citing papers in PubMed, 44 citations in OpenAlex.

  1. Trial
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  5. Article
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  7. Review
  8. Review
  9. Article
  10. Recreating Human Skin In Vitro: Should the Microbiota Be Taken into Account?International journal of molecular sciences · 2024
    Review
  11. Review
  12. Article
  13. Regulatory Roles of Estrogens in Psoriasis.Journal of clinical medicine · 2022
    Review
  14. Review
  15. Review
  16. Review
  17. Article
  18. Article
  19. Review
  20. Nutrition and Psoriasis.International journal of molecular sciences · 2020
    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

8 authors at 3 institutions in 1 country.

Elwira SmolińskaDepartment of Medical Biology and Genetics, University of Gdańsk, Gdańsk, Poland.
Marta MoskotDepartment of Medical Biology and Genetics, University of Gdańsk, Gdańsk, Poland.
Joanna Jakóbkiewicz-BaneckaDepartment of Medical Biology and Genetics, University of Gdańsk, Gdańsk, Poland.
Grzegorz WęgrzynDepartment of Molecular Biology, University of Gdańsk, Gdańsk, Poland.
Bogdan BaneckiDepartment of Molecular and Cellular Biology, Intercollegiate Faculty of Biotechnology UG-MUG, Gdańsk, Poland.
Aneta Szczerkowska-DoboszDepartment of Dermatology, Venereology and Allergology, Medical University of Gdańsk, Gdańsk, Poland.
Dorota Purzycka-BohdanDepartment of Dermatology, Venereology and Allergology, Medical University of Gdańsk, Gdańsk, Poland.
Magdalena Gabig-CimińskaDepartment of Medical Biology and Genetics, University of Gdańsk, Gdańsk, Poland.ORCID 0000-0002-2664-8724
Gdańsk Medical University · PLInstitute of Biochemistry and Biophysics, Polish Academy of Sciences · PLUniversity of Gdańsk · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Due to its strong proliferation-reducing effects on keratinocytes, and also anti-inflammatory properties, the isoflavone genistein has already been proposed as a possible antipsoriatic compound. As there is still no detailed information on this topic, we examined the effects of genistein by using an in vitro model of both, normal and "psoriasis-like" keratinocytes at this stage of our work exhaustively testing the selected flavonoid in a mono-treated experimental design. Gene expression studies revealed transcriptional changes that confirms known disease-associated pathways and highlights many psoriasis-related genes. Our results suggested that aberrant expression of genes contributing to the progress of psoriasis could be improved by the action of genistein. Genistein prevented "cytokine mix" as well as TNF-α-induced NF-κB nuclear translocation, with no effect on the PI3K signaling cascade, indicating the luck of turning this pathway into NF-κB activation. It could have attenuated TNF-α and LPS-induced inflammatory responses by suppressing ROS activation. Regardless of the type of keratinocyte stimulation used, reduction of cytokine IL-8, IL-20 and CCL2 production (both at RNA and protein level) following genistein treatment was visible. Because investigations of other groups supported our commentary on potential administration of genistein as a potential weapon in the armamentarium against psoriasis, it is believed that this paper should serve to encourage researchers to conduct further studies on this subject.

Indexed as

Cell LineCytokinesEnzyme-Linked Immunosorbent AssayGenisteinHumansKeratinocytesMicroscopy, FluorescenceNF-kappa BPhosphatidylinositol 3-KinasesPhosphorylationPsoriasisReactive Oxygen SpeciesSignal TransductionTumor Necrosis Factor-alphaCytokinesGenisteinNF-kappa BPhosphatidylinositol 3-KinasesReactive Oxygen SpeciesTumor Necrosis Factor-alpha

Identifiers

PMID29444128
PMCPMC5812592
OpenAlexW2789600605

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.