Evidence map›Paper›PMID 25839324›Full record

ArticleCancer biology & therapy2015

The expression of P2X₇ receptors in EPCs and their potential role in the targeting of EPCs to brain gliomas.

Jingqin Fang, Xiao Chen, Shunan Wang, Tian Xie, Xuesong Du, Heng Liu, Sumei Wang, Xue Li, Jinhua Chen, Bo Zhang and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer biology & therapy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.4field-weighted citation impact, top 9% 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

18 citing papers in PubMed, 26 citations in OpenAlex.

  1. The Significance of CXCL1 in Cancer: An Overview of Molecular Mechanisms.International journal of molecular sciences · 2026
    Review
  2. Review
  3. Article
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  6. Article
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  8. Review
  9. Article
  10. Article
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  12. Endothelial CaInternational journal of molecular sciences · 2018
    Review
  13. Article
  14. ATP-induced CaCellular and molecular life sciences : CMLS · 2017
    Review
  15. Review
  16. Purinergic Signalling: Therapeutic Developments.Frontiers in pharmacology · 2017
    Review
  17. Article
  18. 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

13 authors at 4 institutions in 2 countries.

Jingqin Fanga Department of Radiology; Institute of Surgery Research; Daping Hospital; Third Military Medical University ; Chongqing , China.
Xiao Chen
Shunan Wang
Tian Xie
Xuesong Du
Heng Liu
Sumei Wang
Xue Li
Jinhua Chen
Bo Zhang
Huaping Liang
Yizeng Yang
Weiguo Zhang
Army Medical University · CNDaping Hospital · CNPhiladelphia University · USUniversity Gastroenterology · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In order to use endothelial progenitor cells (EPCs) as a therapeutic and imaging probe to overcome antiangiogenic resistance for gliomas, how to enhance proliferation and targeting ability of transplanted EPCs is a high priority. Here, we confirmed, for the first time, the expression of P2X7 receptors in rat spleen-derived EPCs. Activation of P2X7 receptors in EPCs by BzATP promoted cells proliferation and migration, rather than apoptosis. In vivo, the homing of transplanted EPCs after long-term suppression of P2X7 receptors by persistent BBG stimulation was evaluated by MRI, immunohistochemistry and flow cytometry. Compared to the group without BBG treatment, less transplanted EPCs homed to gliomas in the group with BBG treatment, especially integrated into the vessels containing tumor-derived endothelial cells in gliomas. Moreover, western blot showed that CXCL1 expression was downregulated in gliomas with BBG treatment, which meant P2X7 receptors suppression inhibited the homing of EPCs to gliomas through down-regulation of CXCLl expression. Further, effects of P2X7 receptors on C6 glioma cells or gliomas were evaluated at the same dose of BzATP or BBG used in EPCs experiments in vitro and in vivo. MTT assay and MRI revealed that P2X7 receptors exerted no significant promoting effect on C6 glioma cells proliferation, gliomas growth and angiogenesis. Taken together, our findings imply the possibility of promoting proliferation and targeting ability of transplanted EPCs to brain gliomas in vivo through P2X7 receptors, which may provide new perspectives on application of EPCs as a therapeutic and imaging probe to overcome antiangiogenic resistance for gliomas.

Indexed as

AnimalsBrain NeoplasmsCell Line, TumorCell MovementCell ProliferationChemokine CXCL1Down-RegulationEndothelial Progenitor CellsGliomaHumansMaleNeovascularization, PathologicRatsRats, Sprague-DawleyReceptors, Purinergic P2X7Chemokine CXCL1CXCL1 protein, humanP2RX7 protein, humanReceptors, Purinergic P2X7C6 glioma cellsDCE, dynamic contrast enhancedECs, endothelial cellsendothelial progenitor cellsEPCs, endothelial progenitor cellsgliomaGSCs, glioma stem-like cellsHSCs, hematopoietic stem cellsmagnetic resonance imagingMRI, magnetic resonance imagingP2X7 receptorsSDF-1α, Stromal derived factor 1αVEGF, vascular endothelial growth factor

Identifiers

PMID25839324
PMCPMC4623375
OpenAlexW1594956518

What Socratic 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 Socratic graph.