Evidence map›Paper›PMID 25995822›Full record

ArticleBiomolecules & therapeutics2015

Dieckol, a Component of Ecklonia cava, Suppresses the Production of MDC/CCL22 via Down-Regulating STAT1 Pathway in Interferon-γ Stimulated HaCaT Human Keratinocytes.

Na-Jin Kang, Dong-Hwan Koo, Gyeoung-Jin Kang, Sang-Chul Han, Bang-Won Lee, Young-Sang Koh, Jin-Won Hyun, Nam-Ho Lee, Mi-Hee Ko, Hee-Kyoung Kang and 1 more

Open access · greenAbstract read
In one paragraph

Article in Biomolecules & therapeutics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
4.0field-weighted citation impact, top 7% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 35 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Nutrients · 2020
    Article
  9. Article
  10. Anti-Atopic Dermatitis Effect ofMediators of inflammation · 2019
    Article
  11. Article
  12. Article
  13. 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

11 authors at 2 institutions in 1 country.

Na-Jin KangDepartments of Biomedicine & Drug Development.
Dong-Hwan KooDepartments of Biomedicine & Drug Development.
Gyeoung-Jin KangMedicine, School of Medicine.
Sang-Chul HanMedicine, School of Medicine.
Bang-Won LeeMedicine, School of Medicine.
Young-Sang KohDepartments of Biomedicine & Drug Development ; Medicine, School of Medicine.
Jin-Won HyunDepartments of Biomedicine & Drug Development ; Medicine, School of Medicine.
Nam-Ho LeeChemistry, College of Natural Science, Jeju National University, Jeju 690-756.
Mi-Hee KoJeju Biodiversity Research Institute, JejuTechnopark, Jeju 699-943, Republic of Korea.
Hee-Kyoung KangDepartments of Biomedicine & Drug Development ; Medicine, School of Medicine.
Eun-Sook YooDepartments of Biomedicine & Drug Development ; Medicine, School of Medicine.
Jeju National University · KRJeju TechnoPark · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Macrophage-derived chemokine, C-C motif chemokine 22 (MDC/CCL22), is one of the inflammatory chemokines that controls the movement of monocytes, monocyte-derived dendritic cells, and natural killer cells. Serum and skin MDC/CCL22 levels are elevated in atopic dermatitis, which suggests that the chemokines produced from keratinocytes are responsible for attracting inflammatory lymphocytes to the skin. A major signaling pathway in the interferon-γ (IFN-γ)-stimulated inflammation response involves the signal transducers and activators of transcription 1 (STAT1). In the present study, we investigated the anti-inflammatory effect of dieckol and its possible action mechanisms in the category of skin inflammation including atopic dermatitis. Dieckol inhibited MDC/CCL22 production induced by IFN-γ (10 ng/mL) in a dose dependent manner. Dieckol (5 and 10 μM) suppressed the phosphorylation and the nuclear translocation of STAT1. These results suggest that dieckol exhibits anti-inflammatory effect via the down-regulation of STAT1 activation.

Indexed as

DieckolInflammationKeratinocyteMDC/CCL22STAT1

Identifiers

PMID25995822
PMCPMC4428716
OpenAlexW2330601353

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.