Evidence map›Paper›PMID 25222785›Full record

ArticleThe Indian journal of medical research2014

Dipyrone & 2,5-dimethylcelecoxib suppress Th2-related chemokine production in monocyte.

Jeng-Chuan Shiang, Ren-Long Jan, Ming-Kai Tsai, Chong-Chao Hsieh, Hsuan-Fu Kuo, Chang-Hung Kuo, San-Nan Yang, Ming-Yii Huang, Li-Chen Chen, Chih-Hsing Hung

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Article in The Indian journal of medical research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact, top 90% 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

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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

3 citing papers in PubMed, 4 citations in OpenAlex.

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4 · The record

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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

10 authors at 1 institution in 1 country.

Jeng-Chuan Shiang
Ren-Long Jan
Ming-Kai Tsai
Chong-Chao Hsieh
Hsuan-Fu Kuo
Chang-Hung Kuo
San-Nan Yang
Ming-Yii Huang
Li-Chen Chen
Chih-Hsing HungGraduate Institute of Medicine, Kaohsiung Medical University Hospital; Department of Pediatrics, Faculty of Medicine; Department of Pediatrics, Faculty of Pediatrics, College of Medicine, Kaohsiung Medical University; Department of Pediatrics, Kaohsiung Municipal Hsiao-Kang Hospital, Kaohsiung, Taiwan.
Kaohsiung Medical University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND &

objectivesSelective cyclooxygenase-2 (COX-2) inhibitor is a form of thnon steroidal anti-inflammatory drug (NSAID) and is commonly used in autoimmune and rheumatic diseases to control inflammation and alleviate pain. Tumour necrosis factor-alpha (TNF-α) production and an imbalance of T helper 1 (Th1)/Th2 contribute to the pathogenesis of autoimmune and also anti-tumour activity. Dipyrone is a NSAID used to treat pain worldwide. The celecoxib analogue, 2,5-dimethylcelecoxib (DMC), lacks COX-2 inhibitory activity but exhibits anti-tumour properties. However, the effects and the mechanisms of dipyrone and 2,5-dimethylcelecoxib on tumour necrosis factor (TNF)-α and Th1- and Th2-related chemokines in monocytes remain poorly defined. This study was carried out to investigate the effects of dipyrone and 2,5-dimethylcelecoxib on the expression of Th1 (IP-10) and Th2 (I-309 and MDC) and TNF-α in human monocytes and the associated intracellular mechanism.

methodsTHP-1 cells and peripheral blood mononuclear cells (PBMCs) were pre-treated with dipyrone (10(-9)-10(-4) M) and 2,5-dimethylcelecoxib (10(-9)-10(-5) M) 2 h before lipopolysaccharide (LPS) stimulation. Cell supernatant was collected 24 h after LPS stimulation. TNF-α, I-309, MDC and IP-10 concentrations of cell supernatants were determined using ELISA. Intracellular signaling was evaluated by w0 estern blot.

resultsDipyrone and 2,5-dimethylcelecoxib downregulated LPS-induced Th2-related chemokine I-309 and macrophage derived chemokine (MDC) production. Only high dose of 2,5-dimethylcelecoxib (10(-5) M), but not dipyrone downregulated LPS-induced IP-10. Only very high dose of 2,5-dimethylcelecoxib had effect on LPS-induced TNF-α expression in PBMCs. Dipyrone and 2,5-dimethylcelecoxib suppressed LPS-induced p65 and JNK MAPK (C-Jun N-terminal kinase mitogen activated protein kinase). expression. INTERPRETATION &

conclusionsDipyrone and 2,5-dimethylcelecoxib downregulated LPS-induced Th2-related chemokine I-309 and MDC in THP-1 cells. The suppressive effect on Th2-related chemokine I-309 and MDC may involve the downregulation of LPS-induced JNK and p65 expression.

Indexed as

ADAM ProteinsAnti-Inflammatory Agents, Non-SteroidalBlotting, WesternChemokine CCL1Chemokine CXCL10ChemokinesDipyroneEnzyme-Linked Immunosorbent AssayGene Expression RegulationHumansMonocytesPyrazolesSulfonamidesTumor Necrosis Factor-alphaTumor Suppressor Proteins2,5-dimethylcelecoxibADAM11 protein, humanADAM ProteinsAnti-Inflammatory Agents, Non-SteroidalCCL1 protein, humanChemokine CCL1Chemokine CXCL10ChemokinesCXCL10 protein, humanDipyronePyrazolesSulfonamidesTumor Necrosis Factor-alphaTumor Suppressor Proteins

Identifiers

PMID25222785
PMCPMC4181142
OpenAlexW2100999373

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LicenceCC BY-NC-SA
Read underepoch 390

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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.