Evidence map›Paper›PMID 24398980›Full record

ArticleInternational journal of molecular sciences2014

Syk/JNK/AP-1 signaling pathway mediates interleukin-6-promoted cell migration in oral squamous cell carcinoma.

Jing-Yuan Chuang, Yuan-Li Huang, Wei-Lin Yen, I-Ping Chiang, Ming-Hsui Tsai, Chih-Hsin Tang

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 1 pooled it
4.3field-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, 1 synthesis or guideline pooled it, 67 citations in OpenAlex.

  1. Pooled it
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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

6 authors at 2 institutions in 1 country.

Jing-Yuan ChuangDepartment of Medical Laboratory Science and Biotechnology, China Medical University, Taichung 402, Taiwan. alise9042@yahoo.com.tw.
Yuan-Li HuangDepartment of Medical Laboratory Science and Biotechnology, China Medical University, Taichung 402, Taiwan. yuanli@asia.edu.tw.
Wei-Lin YenDepartment of Medical Laboratory Science and Biotechnology, China Medical University, Taichung 402, Taiwan. wielin@pchome.com.tw.
I-Ping ChiangDepartment of Medical Laboratory Science and Biotechnology, China Medical University, Taichung 402, Taiwan. d6868@mail.cmuh.org.tw.
Ming-Hsui TsaiDepartment of Medical Laboratory Science and Biotechnology, China Medical University, Taichung 402, Taiwan. minghsui@mail.cmuh.org.tw.
Chih-Hsin TangDepartment of Medical Laboratory Science and Biotechnology, China Medical University, Taichung 402, Taiwan. chtang@mail.cmu.edu.tw.
China Medical University · TWAsia University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oral squamous cell carcinoma (OSCC) typically migrates and metastasizes. Interleukin-6 (IL-6) is a multifunctional cytokine associated with disease status and cancer outcomes. The effect of IL-6 on human OSCC cells, however, is unknown. Here, we showed that IL-6 increased cell migration and Intercellular adhesion molecule-1 (ICAM-1) expression in OSCC cells. Pretreatment of OSCC cells with IL-6R monoclonal antibody (mAb) significantly abolished IL-6-induced cell migration and ICAM-1 expression. By contrast, IL-6-mediated cell motility and ICAM-1 upregulation were attenuated by the Syk and c-Jun N-terminal kinase (JNK) inhibitors. Stimulation of OSCC cells with IL-6 promoted Syk and JNK phosphorylation. Furthermore, IL-6 enhanced AP-1 activity, and the IL-6R mAb, Syk inhibitor, or JNK inhibitor all reduced IL-6-mediated c-Jun phosphorylation, c-Jun binding to the ICAM-1 promoter, and c-Jun translocation into the nucleus. Our results indicate that IL-6 enhances the migration of OSCC cells by increasing ICAM-1 expression through the IL-6R receptor and the Syk, JNK, and AP-1 signal transduction pathways.

Indexed as

AnthracenesAntibodies, MonoclonalCarcinoma, Squamous CellCell Line, TumorCell MovementHumansIntercellular Adhesion Molecule-1Interleukin-6Interleukin-6 InhibitorsJNK Mitogen-Activated Protein KinasesMouth NeoplasmsPhosphorylationReceptor Protein-Tyrosine KinasesReceptors, Interleukin-6RNA InterferenceRNA, Small InterferingAnthracenesAntibodies, MonoclonalIntercellular Adhesion Molecule-1Interleukin-6Interleukin-6 InhibitorsJNK Mitogen-Activated Protein KinasespyrazolanthroneReceptor Protein-Tyrosine KinasesReceptors, Interleukin-6RNA, Small InterferingTranscription Factor AP-1TYRO3 protein, human

Identifiers

PMID24398980
PMCPMC3907824
OpenAlexW2012729913

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.