Evidence map›Paper›PMID 30847950›Full record

ArticleJournal of cellular physiology2019

ELP2 negatively regulates osteoblastic differentiation impaired by tumor necrosis factor α in MC3T3-E1 cells through STAT3 activation.

Chang-Peng Xu, Hong-Tao Sun, Ya-Jun Yang, Zhuang Cui, Jian Wang, Bin Yu, Fa-Zheng Wang, Qing-Po Yang, Yong Qi

Open access · hybridAbstract read
In one paragraph

Article in Journal of cellular physiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

11 citing papers in PubMed, 18 citations in OpenAlex.

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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

9 authors at 4 institutions in 1 country.

Chang-Peng XuDepartment of Orthopaedics, Guangdong Second Provincial General Hospital, Guangzhou, Guangdong, People's Republic of China.ORCID 0000-0001-6349-0842
Hong-Tao SunDepartment of Orthopaedics, Guangdong Second Provincial General Hospital, Guangzhou, Guangdong, People's Republic of China.
Ya-Jun YangDepartment of Pharmacology, Guangdong Medical University, Zhanjiang, Guangdong, People's Republic of China.
Zhuang CuiDepartment of Orthopaedics and Traumatology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, People's Republic of China.
Jian WangDepartment of Orthopaedics, The Inner Mongolia People's Hospital, Hohhot, Inner Mongolia, People's Republic of China.
Bin YuDepartment of Orthopaedics and Traumatology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, People's Republic of China.
Fa-Zheng WangDepartment of Orthopaedics, The First People's Hospital of Kashgar Prefecture, Kashgar, Xinjiang, People's Republic of China.
Qing-Po YangDepartment of Orthopaedics, The First People's Hospital of Kashgar Prefecture, Kashgar, Xinjiang, People's Republic of China.
Yong QiDepartment of Orthopaedics, Guangdong Second Provincial General Hospital, Guangzhou, Guangdong, People's Republic of China.
Guangdong Provincial People's Hospital · CNNanfang Hospital · CNGuangdong Medical College · CNInner Mongolia People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor necrosis factor-α (TNF-α) is a pluripotent signaling molecule. The biological effect of TNF-α includes slowing down osteogenic differentiation, which can lead to bone dysplasia in long-term inflammatory microenvironments. Signal transducer and activator of transcription 3 (STAT3)-interacting protein 1 (StIP1, also known as elongator complex protein 2, ELP2) play a role in inhibiting TNF-α-induced osteoblast differentiation. In the present study, we investigated whether and how ELP2 activation mediates the effects of TNF-α on osteoblastic differentiation. Using in vitro cell cultures of preosteoblastic MC3T3-E1 cells, we found that TNF-α inhibited osteoblastic differentiation accompanied by an increase in ELP2 expression and STAT3 activation. Forced ELP2 expression inhibited osteogenic differentiation of MC3T3-E1 cells, with a decrease in the expression of osteoblast marker genes, alkaline phosphatase activity, and matrix mineralization capacity. In contrast, ELP2 silencing ameliorated osteogenic differentiation in MC3T3-E1 cells, even after TNF-α stimulation. The TNF-α-induced inhibitory effect on osteoblastic differentiation was therefore mediated by ELP2, which was associated with Janus kinase 2 (JAK2)/STAT3 activation. These results suggest that ELP2 is upregulated at the differentiation of MC3T3-E1 cells into osteoblasts and inhibits osteogenic differentiation in response to TNF-α through STAT3 activation.

Indexed as

3T3 CellsAnimalsCell DifferentiationIntracellular Signaling Peptides and ProteinsJanus Kinase 2MiceOsteoblastsOsteogenesisSignal TransductionSTAT3 Transcription FactorTumor Necrosis Factor-alphaELP2 protein, humanElp2 protein, mouseIntracellular Signaling Peptides and ProteinsJak2 protein, mouseJanus Kinase 2Stat3 protein, mouseSTAT3 Transcription FactorTNF protein, humanTumor Necrosis Factor-alphaELP2osteoblastic differentiationsignal transducer and activator of transcription 3tumor necrosis factor-α

Identifiers

PMID30847950
PMCPMC6618314
OpenAlexW2921630389

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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.