Evidence map›Paper›PMID 27338330›Full record

ArticleMolecules (Basel, Switzerland)2016

Syk and IRAK1 Contribute to Immunopharmacological Activities of Anthraquinone-2-carboxlic Acid.

Jae Gwang Park, Young-Jin Son, Mi-Yeon Kim, Jae Youl Cho

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
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

12 citing papers in PubMed.

  1. Article
  2. Safety and tolerability of Pau d' Arco (Advances in integrative medicine · 2022
    Article
  3. Anti-Inflammatory Functions of Methanol Extract fromPlants (Basel, Switzerland) · 2022
    Article
  4. Article
  5. Molecules (Basel, Switzerland) · 2020
    Review
  6. AKT-targeted anti-inflammatory activity ofJournal of ginseng research · 2018
    Article
  7. Phosphatidylinositide 3-Kinase Contributes to the Anti-Inflammatory Effect ofEvidence-based complementary and alternative medicine : eCAM · 2018
    Article
  8. Tabetri™ (Mediators of inflammation · 2018
    Article
  9. Article
  10. Article
  11. Tabetri™ (Mediators of inflammation · 2017
    Article
  12. 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

4 authors.

Jae Gwang ParkDepartment of Genetic Engineering, Sungkyunkwan University, Suwon 16419, Korea. wannabejk@naver.com.
Young-Jin SonDepartment of Pharmacy, Sunchon National University, Suncheon 57922, Korea. sony@sunchon.ac.kr.
Mi-Yeon KimSchool of Systems Biomedical Science, Soongsil University, Seoul 06978, Korea. kimmy@ssu.ac.kr.
Jae Youl ChoDepartment of Genetic Engineering, Sungkyunkwan University, Suwon 16419, Korea. jaecho@skku.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Anthraquinone-2-carboxlic acid (9,10-dihydro-9,10-dioxo-2-anthracenecarboxylic acid, AQCA) was identified as one of the major anthraquinones in Brazilian taheebo. Since there was no report explaining its immunopharmacological actions, in this study, we aimed to investigate the molecular mechanism of AQCA-mediated anti-inflammatory activity using reporter gene assays, kinase assays, immunoblot analyses, and overexpression strategies with lipopolysaccharide (LPS)-treated macrophages. AQCA was found to suppress the release of nitric oxide (NO) and prostaglandin (PG) E₂ from LPS-treated peritoneal macrophages without displaying any toxic side effects. Molecular analysis revealed that AQCA was able to inhibit the activation of the nuclear factor (NF)-κB and activator protein (AP)-1 pathways by direct suppression of upstream signaling enzymes including interleukin-1 receptor-associated kinase 1 (IRAK1) and spleen tyrosine kinase (Syk). Therefore, our data strongly suggest that AQCA-mediated suppression of inflammatory responses could be managed by a direct interference of signaling cascades including IRAK and Syk, linked to the activation of NF-κB and AP-1.

Indexed as

AnthraquinonesAnti-Inflammatory AgentsBrazilHumansInflammationInterleukin-1 Receptor-Associated KinasesLipopolysaccharidesMacrophages, PeritonealNF-kappa BNitric OxideProstaglandinsSyk KinaseTabebuiaTranscription Factor AP-1anthraquinone-2-carboxylic acidAnthraquinonesAnti-Inflammatory AgentsInterleukin-1 Receptor-Associated KinasesIRAK1 protein, humanLipopolysaccharidesNF-kappa BNitric OxideProstaglandinsSyk KinaseTranscription Factor AP-1anthraquinone-2-carboxylic acidanthraquinonesinflammatory responseIRAK1

Identifiers

PMID27338330
PMCPMC6272897

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Registered trials

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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.