Evidence map›Paper›PMID 24466366›Full record

ArticleTranslational oncology2013

Ionizing radiation and glioblastoma exosomes: implications in tumor biology and cell migration.

W Tris Arscott, Anita T Tandle, Shuping Zhao, Jacob E Shabason, Ira K Gordon, Cody D Schlaff, Guofeng Zhang, Philip J Tofilon, Kevin A Camphausen

Open access · goldAbstract read
In one paragraph

Article in Translational oncology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 137 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
137citing papers in PubMed, 1 pooled it
3.9field-weighted citation impact, top 6% 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

137 citing papers in PubMed, 1 synthesis or guideline pooled it, 231 citations in OpenAlex.

  1. Pooled it
  2. Thbs1Journal of advanced research · 2026
    Article
  3. Blood derived extracellular vesicles in patients with glioblastoma: preliminary experience from a monoinstitutional series.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Review
  11. HIG-2 promotes glioma stemness and radioresistance mediated by IGFBP2-rich microparticles in hypoxia.Apoptosis : an international journal on programmed cell death · 2025
    Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Review

77 more citing papers are in PubMed but not listed here.

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 3 institutions in 1 country.

W Tris ArscottRadiation Oncology Branch, National Cancer Institute, Bethesda, MD ; University of Vermont College of Medicine, Burlington, VT ; Howard Hughes Medical Institute-National Institutes of Health Research Scholars Program, Bethesda, MD.
Anita T TandleRadiation Oncology Branch, National Cancer Institute, Bethesda, MD.
Shuping ZhaoRadiation Oncology Branch, National Cancer Institute, Bethesda, MD.
Jacob E ShabasonRadiation Oncology Branch, National Cancer Institute, Bethesda, MD ; Howard Hughes Medical Institute-National Institutes of Health Research Scholars Program, Bethesda, MD ; Department of Radiation Oncology, University of Pennsylvania School of Medicine, Philadelphia, PA.
Ira K GordonRadiation Oncology Branch, National Cancer Institute, Bethesda, MD.
Cody D SchlaffRadiation Oncology Branch, National Cancer Institute, Bethesda, MD.
Guofeng ZhangBiomedical Engineering and Physical Science Shared Resource, National Institute of Biomedical Imaging and Bioengineering, Bethesda, MD.
Philip J TofilonRadiation Oncology Branch, National Cancer Institute, Bethesda, MD.
Kevin A CamphausenRadiation Oncology Branch, National Cancer Institute, Bethesda, MD.
National Cancer Institute · USNational Institute of Biomedical Imaging and Bioengineering · USNational Institutes of Health · US

Funding

Electron MicroscopyZICEB000080 · NIBIB · NATIONAL INSTITUTE OF BIOMEDICAL IMAGING AND BIOENGINEERING · PI ZHANG, GUOFENG · 2011 to 2025
$8.2M
6 · The paper itself

Abstract

Exosomes are nanometer-sized lipid vesicles released ubiquitously by cells, which have been shown to have a normal physiological role, as well as influence the tumor microenvironment and aid metastasis. Recent studies highlight the ability of exosomes to convey tumor-suppressive and oncogenic mRNAs, microRNAs, and proteins to a receiving cell, subsequently activating downstream signaling pathways and influencing cellular phenotype. Here, we show that radiation increases the abundance of exosomes released by glioblastoma cells and normal astrocytes. Exosomes derived from irradiated cells enhanced the migration of recipient cells, and their molecular profiling revealed an abundance of molecules related to signaling pathways important for cell migration. In particular, connective tissue growth factor (CTGF) mRNA and insulin-like growth factor binding protein 2 (IGFBP2) protein levels were elevated, and coculture of nonirradiated cells with exosomes isolated from irradiated cells increased CTGF protein expression in the recipient cells. Additionally, these exosomes enhanced the activation of neurotrophic tyrosine kinase receptor type 1 (TrkA), focal adhesion kinase, Paxillin, and proto-oncogene tyrosine-protein kinase Src (Src) in recipient cells, molecules involved in cell migration. Collectively, our data suggest that radiation influences exosome abundance, specifically alters their molecular composition, and on uptake, promotes a migratory phenotype.

Identifiers

PMID24466366
PMCPMC3890698
OpenAlexW1994878006

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.