Evidence map›Paper›PMID 28616734›Full record

ArticleInflammation research : official journal of the European Histamine Research Society ... [et al.]2017

Di-2-pyridylketone 4,4-dimethyl-3-thiosemicarbazone (Dp44mT), an anticancer agent, exerts an anti-inflammatory effect in activated human mast cells.

Sun-Young Nam, Na-Ra Han, Kyoung Wan Yoon, Hyung-Min Kim, Hyun-Ja Jeong

Abstract read
PubMed Publisher
In one paragraph

Article in Inflammation research : official journal of the European Histamine Research Society ... [et al.], 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

10 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Emerging Roles of the Iron Chelators in Inflammation.International journal of molecular sciences · 2022
    Review
  6. Review
  7. Trigonelline, An Alkaloid FromFrontiers in pharmacology · 2021
    Article
  8. Role of Mast Cells in Shaping the Tumor Microenvironment.Clinical reviews in allergy & immunology · 2020
    Review
  9. Article
  10. 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

5 authors at 2 institutions in 1 country.

Sun-Young NamDepartment of Pharmacology, College of Korean Medicine, Kyung Hee University, Seoul, Republic of Korea.
Na-Ra HanDepartment of Pharmacology, College of Korean Medicine, Kyung Hee University, Seoul, Republic of Korea.
Kyoung Wan YoonDepartment of Biotechnology, Hoseo University, 20, Asan, Republic of Korea.
Hyung-Min KimDepartment of Pharmacology, College of Korean Medicine, Kyung Hee University, Seoul, Republic of Korea. hmkim@khu.ac.kr.
Hyun-Ja JeongDepartment of Food Science and Technology, Hoseo University, 20, Asan, Republic of Korea. hjjeong@hoseo.edu.
Kyung Hee University · KRHoseo University · KR

Funding

National Research Foundation of Korea 2015R1A1A3A04000922
6 · The paper itself

Abstract

objectiveInflammation has been closely associated with the development and progression of cancer. Previously, we reported that mast cells play a critical role in tumor growth. The purpose of this study is to investigate the anti-inflammatory effect of an anticancer agent, di-2-pyridylketone 4,4-dimethyl-3-thiosemicarbazone (Dp44mT), on an activated human mast cell line, in this case HMC-1 cells.

methodsWe evaluated the effect and specific molecular mechanism of Dp44mT on phorbol 12-myristate 13-acetate and calcium ionophore A23187 (PMACI) using HMC-1 cells.

resultsHere, we demonstrated that Dp44mT significantly decreased the protein levels of hypoxia-inducible factor-1α and vascular endothelial growth factor without exposing activated HMC-1 cells to any cytotoxicity. In activated mast cells, Dp44mT mitigated the strong production and mRNA expression of inflammatory cytokines, in this case, interleukin (IL)-1β, IL-6, tumor necrosis factor-α, and thymic stromal lymphopoietin, through a blockade of caspase-1 and nuclear factor-κB activities. Furthermore, phosphorylations of the mitogen-activated protein kinase family included in inflammatory signaling cascades were significantly inhibited by a Dp44mT treatment.

conclusionsOverall, our results indicate that the anticancer agent Dp44mT has an anti-inflammatory effect and may be of therapeutic importance for the treatment of mast cell-mediated inflammatory diseases.

Indexed as

Anti-Inflammatory AgentsAntineoplastic AgentsCalcimycinCaspase InhibitorsCell LineCytokinesHumansHypoxia-Inducible Factor 1IonophoresMAP Kinase Signaling SystemMast CellsNF-kappa BRNA, MessengerTetradecanoylphorbol AcetateThiosemicarbazonesThymic Stromal LymphopoietinAnti-Inflammatory AgentsAntineoplastic AgentsCalcimycinCaspase InhibitorsCytokinesdi-2-pyridylketone-4,4-dimethyl-3-thiosemicarbazoneHypoxia-Inducible Factor 1IonophoresNF-kappa BRNA, MessengerTetradecanoylphorbol AcetateThiosemicarbazonesThymic Stromal LymphopoietinVascular Endothelial Growth Factor AVEGFA protein, humanAnticancer agentDp44mTHypoxia-inducible factor-1αMast cellThymic stromal lymphopoietinVascular endothelial growth factor

Identifiers

PMID28616734
OpenAlexW2626816033

What OpenQuestion holds

Textmetadata
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.