Evidence map›Paper›PMID 29449895›Full record

ArticleTherapeutic advances in medical oncology2017

DNM3, p65 and p53 from exosomes represent potential clinical diagnosis markers for glioblastoma multiforme.

Jian-Kai Yang, Jian Song, Hao-Ran Huo, Yin-Long Zhao, Guang-Yu Zhang, Zong-Mao Zhao, Guo-Zhu Sun, Bao-Hua Jiao

Open access · goldAbstract read
In one paragraph

Article in Therapeutic advances in medical oncology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

26 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
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  7. Relationship between exosomes and cancer: formation, diagnosis, and treatment.International journal of biological sciences · 2025
    Review
  8. Review
  9. Review
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  11. Exosomes as Novel Diagnostic Biomarkers and Therapeutic Tools in Gliomas.International journal of molecular sciences · 2023
    Review
  12. Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Review
  18. Role of Exosomes in the Progression, Diagnosis, and Treatment of Gliomas.Medical science monitor : international medical journal of experimental and clinical research · 2020
    Review
  19. Review
  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

8 authors at 2 institutions in 1 country.

Jian-Kai YangDepartment of Neurosurgery, The Second Hospital of Hebei Medical University, Shijiazhuang, China.
Jian SongDepartment of Neurosurgery, The Second Hospital of Hebei Medical University, Shijiazhuang, China.
Hao-Ran HuoDepartment of Neurosurgery, The Second Hospital of Hebei Medical University, Shijiazhuang, China.
Yin-Long ZhaoDepartment of Neurosurgery, The Second Hospital of Hebei Medical University, Shijiazhuang, China.
Guang-Yu ZhangDepartment of Neurosurgery, The Second Hospital of Hebei Medical University, Shijiazhuang, China.
Zong-Mao ZhaoDepartment of Neurosurgery, The Second Hospital of Hebei Medical University, Shijiazhuang, China.
Guo-Zhu SunDepartment of Neurosurgery, The Second Hospital of Hebei Medical University, Shijiazhuang, China.
Bao-Hua JiaoDepartment of Neurosurgery, The Second Hospital of Hebei Medical University, 215 Hepingxi Road, Shijiazhuang 050000, China.
Hebei Medical University · CNSecond Hospital of Hebei Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGlioblastoma multiforme (GBM) is the most aggressive and deadly primary brain cancer that arises from astrocytes and classified as grade IV. Recently, exosomes have been reported as an essential mediator in diverse cancer carcinogenesis and metastasis. However, their role in GBM is still unclear. In this study, we aimed to investigate whether blood exosomes can be potential clinical diagnostic markers for GBM.

methodsWe used a xenograft orthotopic mouse model to detect the differentially expressed genes in the brain and blood exosomes of original/recurrent GBM.

resultsWe found that recurrent GBM had stronger growth capacity and lethality than original GBM in the mouse model. A gene microarray of original tumors and blood exosomes from GBM orthotopic xenografts results showed that DNM3, p65 and CD117 expressions increased, whereas PTEN and p53 expressions decreased in both original tumors and blood exosomes. In the recurrent GBM tumor model, DNM3 and p65 showed increased expressions, whereas ST14 and p53 showed decreased expressions in tumor and blood exosomes of the recurrent GBM mouse model.

conclusionIn summary, we found that DNM3, p65 and p53 had a similar trend in brain and blood exosomes both for original and recurrent GBM, and could serve as potential clinical diagnostic markers for GBM.

Indexed as

DNM3exosomesglioblastoma multiforme (GBM)p53p65

Identifiers

PMID29449895
PMCPMC5808838
OpenAlexW2767256140

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.