Evidence map›Paper›PMID 33193420›Full record

ArticleFrontiers in immunology2020

Sulforaphane Promotes Dendritic Cell Stimulatory Capacity Through Modulation of Regulatory Molecules, JAK/STAT3- and MicroRNA-Signaling.

Yangyi Wang, Emilia Petrikova, Wolfgang Gross, Carsten Sticht, Norbert Gretz, Ingrid Herr, Svetlana Karakhanova

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

17 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Sulforaphane activates CD8Journal for immunotherapy of cancer · 2024
    Article
  11. Review
  12. Article
  13. Review
  14. Review
  15. Review
  16. Article
  17. Phytochemicals in Cancer Chemoprevention: Preclinical and Clinical Studies.Cancer control : journal of the Moffitt Cancer Center
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

Yangyi WangSection Surgical Research, Molecular OncoSurgery Group, Department of General, Visceral and Transplantation Surgery, University of Heidelberg, Heidelberg, Germany.
Emilia PetrikovaSection Surgical Research, Molecular OncoSurgery Group, Department of General, Visceral and Transplantation Surgery, University of Heidelberg, Heidelberg, Germany.
Wolfgang GrossSection Surgical Research, Molecular OncoSurgery Group, Department of General, Visceral and Transplantation Surgery, University of Heidelberg, Heidelberg, Germany.
Carsten StichtMedical Research Center, Medical Faculty Mannheim, University of Heidelberg, Mannheim, Germany.
Norbert GretzMedical Research Center, Medical Faculty Mannheim, University of Heidelberg, Mannheim, Germany.
Ingrid HerrSection Surgical Research, Molecular OncoSurgery Group, Department of General, Visceral and Transplantation Surgery, University of Heidelberg, Heidelberg, Germany.
Svetlana KarakhanovaSection Surgical Research, Molecular OncoSurgery Group, Department of General, Visceral and Transplantation Surgery, University of Heidelberg, Heidelberg, Germany.
Heidelberg University · DEUniversity Hospital Heidelberg · DEUniversity Medical Centre Mannheim · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: The broccoli isothiocyanate sulforaphane was shown to inhibit inflammation and tumor progression, also in pancreatic cancer, while its effect on tumor immunity is poorly understood. We investigated the immunoregulatory effect of sulforaphane on human dendritic cells alone and in presence of pancreatic tumor antigens, as well as underlying molecular mechanisms. Methods: Sulforaphane-treated human dendritic cells were matured Results: Sulforaphane modulated the expression of the costimulatory CD80, CD83 and the suppressive B7-H1 molecules on dendritic cells and thereby promoted activation of T cells. The effect was verified in presence of pancreatic tumor antigens. Phosphorylation of STAT3 in dendritic cells was diminished by sulforaphane, and the inhibition of JAK/STAT3 led to downregulation of B7-H1 expression. Among the identified top 100 significant microRNA candidates, the inhibition of miR-155-5p, important for the expression of costimulatory molecules, and the induction of miR-194-5p, targeting the B7-H1 gene, were induced by sulforaphane. Conclusion: Our findings demonstrate that sulforaphane promotes T-cell activation by dendritic cells through the modulation of regulatory molecules, JAK/STAT3- and microRNA-signaling in healthy conditions and in context of pancreatic cancer-derived antigens. They explore the immunoregulatory properties of sulforaphane and justify further research on nutritional strategies in the co-treatment of cancer.

Indexed as

Antigens, CDB7-1 AntigenB7-H1 AntigenCD83 AntigenCell Line, TumorCell ProliferationDendritic CellsHumansImmunoglobulinsImmunologic FactorsIsothiocyanatesJanus KinasesMembrane GlycoproteinsMicroRNAsSignal TransductionSTAT3 Transcription FactorAntigens, CDB7-1 AntigenB7-H1 AntigenCD274 protein, humanCD80 protein, humanCD83 AntigenImmunoglobulinsImmunologic FactorsIsothiocyanatesJanus KinasesMembrane GlycoproteinsMicroRNAsSTAT3 protein, humanSTAT3 Transcription FactorsulforaphaneSulfoxidesdendritic cellsmiRNAspancreatic cancerregulatory moleculesSTAT3sulforaphaneT cells

Identifiers

PMID33193420
PMCPMC7661638
OpenAlexW3096571347

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.