Evidence map›Paper›PMID 20823154›Full record

ArticleCancer research2010

Angiopoietin-4 promotes glioblastoma progression by enhancing tumor cell viability and angiogenesis.

Melissa K Brunckhorst, Hui Wang, Rong Lu, Qin Yu

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 10% 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

42 citing papers in PubMed, 1 synthesis or guideline pooled it, 63 citations in OpenAlex.

  1. Dynamic Remodeling of Oocyte-Granulosa Cell Communication During Bovine Folliculogenesis Revealed by Transcriptomic Meta-Analyses.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Pooled it
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  6. Flavonoid-Mediated Suppression of Tumor Angiogenesis: Roles of Ang-Tie/PI3K/AKT.Pathophysiology : the official journal of the International Society for Pathophysiology · 2024
    Review
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  10. Article
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  13. Tumor Vessels Fuel the Fire in Glioblastoma.International journal of molecular sciences · 2021
    Review
  14. Angiopoietins as Potential Targets in Management of Retinal Disease.Clinical ophthalmology (Auckland, N.Z.) · 2021
    Review
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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

4 authors at 2 institutions in 1 country.

Melissa K BrunckhorstDepartment of Oncological Sciences, Mount Sinai School of Medicine, New York, New York, USA.
Hui Wang
Rong Lu
Qin Yu
University of Pennsylvania · USIcahn School of Medicine at Mount Sinai · US

Funding

Angiopoietins in AngiogenesisR01HL074117 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI YU, QIN · 2003 to 2006
$1.3M
NHLBI NIH HHS R01 HL074117NHLBI NIH HHS R01HL074117
6 · The paper itself

Abstract

Glioblastoma multiforme (GBM) is a highly invasive and vascularized aggressive brain tumor. Less than 10% of GBM patients survive >5 years after diagnosis. Angiogenesis plays an important role in GBM growth, and antiangiogenesis-based therapies have shown clinical efficacy for GBM patients. Unfortunately, therapeutic resistance often develops in these patients, suggesting that GBM cells are capable of switching their dependency on one proangiogenic signaling pathway to an alternative one. Therefore, it is important to identify novel angiogenic factors that play essential roles in tumor angiogenesis and GBM progression. Angiopoietins (Ang-1, Ang-2, and Ang-4) are the ligands of the Tie-2 receptor tyrosine kinase (RTK). The roles of Ang-1 and Ang-2 in tumor angiogenesis have been established. However, little is known about how Ang-4 affects tumor angiogenesis and GBM progression and the mechanism underlying its effects. In our current study, we establish that Ang-4 is upregulated in human GBM tissues and cells. We show that, like endothelial cells, human GBM cells express Tie-2 RTK. We first establish that Ang-4 promotes in vivo growth of human GBM cells by promoting tumor angiogenesis and directly activating extracellular signal-regulated kinase 1/2 (Erk1/2) in GBM cells. Our results establish the novel effects of Ang-4 on tumor angiogenesis and GBM progression and suggest that this pro-GBM effect of Ang-4 is mediated by promoting tumor angiogenesis and activating Erk1/2 kinase in GBM cells. Together, our results suggest that the Ang-4-Tie-2 functional axis is an attractive therapeutic target for GBM.

Indexed as

AngiopoietinsBrain NeoplasmsCell Growth ProcessesCell SurvivalDisease ProgressionGene Expression Regulation, NeoplasticGlioblastomaHumansMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Neovascularization, PathologicReceptor, TIE-2RNA, MessengerUp-Regulationangiopoietin 4AngiopoietinsMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Receptor, TIE-2RNA, Messenger

Identifiers

PMID20823154
PMCPMC2940950
OpenAlexW2151970171

What OpenQuestion holds

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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.