Evidence map›Paper›PMID 27278519›Full record

ArticleJournal of neuro-oncology2016

Inhibition of pentraxin 3 in glioma cells impairs proliferation and invasion in vitro and in vivo.

Jai-Nien Tung, Chung-Po Ko, Shun-Fa Yang, Chun-Wen Cheng, Pei-Ni Chen, Chia-Yu Chang, Chia-Liang Lin, Te-Fang Yang, Yi-Hsien Hsieh, Kun-Chung Chen

Abstract read
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In one paragraph

Article in Journal of neuro-oncology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

22 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
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  4. Review
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  6. Article
  7. Role of long pentraxin PTX3 in cancer.Clinical and experimental medicine · 2023
    Review
  8. The evaluation of six genes combined value in glioma diagnosis and prognosis.Journal of cancer research and clinical oncology · 2023
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. STAT3 Activates the Pentraxin 3 Gene in Chronic Lymphocytic Leukemia Cells.Journal of immunology (Baltimore, Md. : 1950) · 2022
    Article
  14. Article
  15. Review
  16. Article
  17. Article
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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

10 authors at 3 institutions in 1 country.

Jai-Nien TungDepartment of Neurosurgery, Tungs' Taichung MetroHarbor Hospital, Taichung, Taiwan.
Chung-Po KoDepartment of Neurosurgery, Tungs' Taichung MetroHarbor Hospital, Taichung, Taiwan.
Shun-Fa YangInstitute of Medicine, Chung Shan Medical University, Taichung, Taiwan.
Chun-Wen ChengInstitute of Biochemistry, Microbiology and Immunology, Chung Shan Medical University, Taichung, Taiwan.
Pei-Ni ChenInstitute of Biochemistry, Microbiology and Immunology, Chung Shan Medical University, Taichung, Taiwan.
Chia-Yu ChangInstitute of Biochemistry, Microbiology and Immunology, Chung Shan Medical University, Taichung, Taiwan.
Chia-Liang LinInstitute of Biochemistry, Microbiology and Immunology, Chung Shan Medical University, Taichung, Taiwan.
Te-Fang YangInstitute of Biochemistry, Microbiology and Immunology, Chung Shan Medical University, Taichung, Taiwan.
Yi-Hsien HsiehInstitute of Biochemistry, Microbiology and Immunology, Chung Shan Medical University, Taichung, Taiwan. hyhsien@csmu.edu.tw.
Kun-Chung ChenPhysical Therapy Room, Chung Shan Medical University Hospital, Taichung, Taiwan. kunchung@seed.net.tw.
Chung Shan Medical University · TWChung Shan Medical University Hospital · TWTungs' Taichung MetroHarbor Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pentraxin 3 (PTX3) is an inflammatory molecule that is involved in immune responses, inflammation, and cancer. Recent evidence suggests that PTX3 plays a critical role in tumor progression; however, its impact on the biological function of gliomas remains unknown. In the present study, immunohistochemical staining showed that patients with high-grade gliomas exhibited increased expression levels of PTX3 compared to those with low-grade gliomas (P < 0.001). Furthermore, knockdown of PTX3 in GBM8401 cells inhibits proliferation, increases p21 protein levels, and decreases cyclin D1 protein levels, resulting in cell cycle arrest at the G0/G1 phase. In addition, knockdown of PTX3 significantly decreases GBM8401 cell migration and invasion through the downregulation of matrix metalloproteinase-1 and -2 (MMP-1 and MMP-2) expression. In a GBM8401 xenograft animal model, PTX3 knockdown decreases tumor growth in vivo. In conclusion, PTX3 plays an important role in glioma cell proliferation and invasion, and may thus serve as a novel potential therapeutic target in the treatment of gliomas.

Indexed as

AdultAgedAnimalsBrain NeoplasmsCell CycleCell Cycle CheckpointsCell Line, TumorCell MovementCell ProliferationC-Reactive ProteinDisease Models, AnimalFemaleGene Expression Regulation, NeoplasticGliomaHumansMatrix Metalloproteinase 1C-Reactive ProteinMatrix Metalloproteinase 1Matrix Metalloproteinase 9PentraxinsRNA, Small InterferingSerum Amyloid P-ComponentGliomasInvasionMigrationPentraxin 3Proliferation

Identifiers

PMID27278519
OpenAlexW2414669011

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.