Evidence map›Paper›PMID 27572279›Full record

ArticleMolecular medicine reports2016

Curcumin inhibits osteoclastogenic potential in PBMCs from rheumatoid arthritis patients via the suppression of MAPK/RANK/c-Fos/NFATc1 signaling pathways.

Wei Shang, Ling-Jie Zhao, Xiao-Lei Dong, Zhi-Ming Zhao, Jing Li, Bei-Bei Zhang, Hui Cai

Open access · hybridAbstract read
In one paragraph

Article in Molecular medicine reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 3 pooled it
4.5field-weighted citation impact, top 5% 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

37 citing papers in PubMed, 3 syntheses or guidelines pooled it, 77 citations in OpenAlex.

  1. Pooled it
  2. Efficacy and Safety of Curcumin andFrontiers in immunology · 2022
    Pooled it
  3. Molecular insights into phytochemicals exhibiting anti-arthritic activity: systematic review : John Di Battista.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2021
    Pooled it
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  11. Advanced biomedical research · 2024
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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

7 authors at 2 institutions in 1 country.

Wei ShangThe First Clinical Medical College, Nanjing University of Chinese Medicine, Nanjing, Jiangsu 210023, P.R. China.
Ling-Jie ZhaoDepartment of Integrated Traditional Chinese and Western Medicine, Jinling Hospital, Nanjing, Jiangsu 210002, P.R. China.
Xiao-Lei DongDepartment of Integrated Traditional Chinese and Western Medicine, Jinling Hospital, Nanjing, Jiangsu 210002, P.R. China.
Zhi-Ming ZhaoDepartment of Integrated Traditional Chinese and Western Medicine, Jinling Hospital, Nanjing, Jiangsu 210002, P.R. China.
Jing LiDepartment of Integrated Traditional Chinese and Western Medicine, Jinling Hospital, Nanjing, Jiangsu 210002, P.R. China.
Bei-Bei ZhangDepartment of Integrated Traditional Chinese and Western Medicine, Jinling Hospital, Nanjing, Jiangsu 210002, P.R. China.
Hui CaiDepartment of Integrated Traditional Chinese and Western Medicine, Jinling Hospital, Nanjing, Jiangsu 210002, P.R. China.
Nanjing General Hospital of Nanjing Military Command · CNNanjing University of Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of the present study was to determine the effects of curcumin on the osteoclastogenic potential of peripheral blood mononuclear cells (PBMCs) obtained from patients with rheumatoid arthritis (RA), and to investigate the underlying molecular mechanisms. PBMCs from patients with RA (n=12) and healthy controls (n=10) were cultured to assess osteoclastogenic potential. The number of tartrate‑resistant acid phosphatase‑positive osteoclasts differentiated from PBMCs isolated from patients with RA was significantly increased compared with that of the healthy controls. In addition, the osteoclast number in patients with RA was correlated with the clinical indicators, Sharp score (r=0.810; P=0.001) and lumbar T‑score (r=‑0.685; P=0.014). Furthermore, the resorption area was increased in the RA group compared with the healthy controls. The mRNA and protein expression levels in PBMC‑derived osteoclasts treated with curcumin were measured by reverse transcription‑quantitative polymerase chain reaction and western blotting, respectively. Curcumin inhibited the osteoclastogenic potential of PBMCs, potentially by suppressing activation of extracellular signal‑regulated kinases 1 and 2, p38 and c‑Jun N‑terminal kinase, and inhibiting receptor activator of nuclear factor κB (RANK), c‑Fos and nuclear factor of activated T cells (NFATc1) expression. The results of the present study demonstrated that curcumin may inhibit the osteoclastogenic potential of PBMCs from patients with RA through the suppression of the mitogen‑activated protein kinase/RANK/c‑Fos/NFATc1 signaling pathways, and that curcumin may be a potential novel therapeutic agent for the treatment of bone deterioration in inflammatory diseases such as RA.

Indexed as

Anti-Inflammatory AgentsArthritis, RheumatoidCell DifferentiationCells, CulturedCurcuminHumansLeukocytes, MononuclearMAP Kinase Signaling SystemNFATC Transcription FactorsOsteoclastsProto-Oncogene Proteins c-fosReceptor Activator of Nuclear Factor-kappa BSignal TransductionAnti-Inflammatory AgentsCurcuminNFATC1 protein, humanNFATC Transcription FactorsProto-Oncogene Proteins c-fosReceptor Activator of Nuclear Factor-kappa BTNFRSF11A protein, human

Identifiers

PMID27572279
PMCPMC5042742
OpenAlexW2510114965

What OpenQuestion holds

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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.