Evidence map›Paper›PMID 26617938›Full record

ArticleInternational journal of clinical and experimental pathology2015

TRAF4 enhances oral squamous cell carcinoma cell growth, invasion and migration by Wnt-β-catenin signaling pathway.

Jianbin Yang, Dongyi Wei, Weixin Wang, Baohong Shen, Suling Xu, Yuan Cao

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

27 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. About a Possible Impact of Endodontic Infections byInternational journal of molecular sciences · 2024
    Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. MicroRNA-31 Regulates Expression ofInternational journal of molecular sciences · 2020
    Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Expression and Association of Tumor Necrosis Factor Receptor Associated Factor 4 (TRAF4) in Esophageal Squamous Cell Carcinoma.Medical science monitor : international medical journal of experimental and clinical research · 2019
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
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 1 institution in 1 country.

Jianbin YangDepartment of Oral and Maxillofacial Surgery, The First Affiliated Hospital of Xinxiang Medial University Weihui 453100, China.
Dongyi WeiDepartment of Oral and Maxillofacial Surgery, The First Affiliated Hospital of Xinxiang Medial University Weihui 453100, China.
Weixin WangDepartment of Oral and Maxillofacial Surgery, The First Affiliated Hospital of Xinxiang Medial University Weihui 453100, China.
Baohong ShenDepartment of Oral and Maxillofacial Surgery, The First Affiliated Hospital of Xinxiang Medial University Weihui 453100, China.
Suling XuDepartment of Oncology, The First Affiliated Hospital of Xinxiang Medial University Weihui 453100, China.
Yuan CaoDepartment of Oral and Maxillofacial Surgery, The First Affiliated Hospital of Xinxiang Medial University Weihui 453100, China.
First Affiliated Hospital of Xinxiang Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oral squamous cell carcinoma (OSCC) ranks as the fifth most common cancer worldwide with poor prognosis. Recently, tumor necrosis factor receptor-associated factor 4 (TRAF4) has attracted increasing attenuation due to its overexpression in certain cancers. However, its function and underlying mechanism in OSCC remains elusive. In this study, the high expression of TRAF4 mRNA and protein levels was noted in OSCC cell lines. Its overexpression with pcDNA3.1-TRAF4 vector transfection dramatically promoted cell proliferation and inhibited cell apoptosis, indicating a pivotal role of TRAF4 in OSCC cell growth. Simultaneously, TRAF4 elevation also increased cell invasion and migration. Mechanism analysis confirmed that TRAF4 up-regulation induced the expression of β-catenin and the downstream target molecules of cyclinD1, c-myc, Bcl-2, MMP-9 and MMP-2, indicating that TRAF4 could induce the activation of Wnt/β-catenin pathway. After pretreatment with β-catenin siRNA, the pathway was remarkably silenced. Simultaneously, cell growth, invasion and migration induced by TRAF4 were strikingly abrogated, suggesting that TRAF4 may promote OSCC cell growth, invasion and migration by Wnt/β-catenin pathway. Together, this study confirmed that TRAF4 acts as an oncogene for the development and progression of OSCC. Therefore, our study may support a promising therapeutic target for the treatment of OSCC.

Indexed as

Cell MovementCell ProliferationWnt Signaling PathwayApoptosisbeta CateninCarcinoma, Squamous CellCell Line, TumorCyclin D1Head and Neck NeoplasmsHumansMatrix Metalloproteinase 2Matrix Metalloproteinase 9Neoplasm InvasivenessProto-Oncogene Proteins c-bcl-2Proto-Oncogene Proteins c-mycRNA InterferenceBCL2 protein, humanbeta CateninCCND1 protein, humanCTNNB1 protein, humanCyclin D1Matrix Metalloproteinase 2Matrix Metalloproteinase 9MMP2 protein, humanMMP9 protein, humanMYC protein, humanProto-Oncogene Proteins c-bcl-2Proto-Oncogene Proteins c-mycTNF Receptor-Associated Factor 4TRAF4 protein, humancell growthcell invasioncell migrationOral squamous cell carcinomaTRAF4Wnt/β-catenin pathway

Identifiers

PMID26617938
PMCPMC4637754
OpenAlexW2225969945

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.