Evidence map›Paper›PMID 18515660›Full record

ArticleBlood2008

Angiostatic activity of the antitumor cytokine interleukin-21.

Karolien Castermans, Sebastien P Tabruyn, Rong Zeng, Judy R van Beijnum, Cheryl Eppolito, Warren J Leonard, Protul A Shrikant, Arjan W Griffioen

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
1.5field-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

31 citing papers in PubMed, 1 synthesis or guideline pooled it, 59 citations in OpenAlex.

  1. Pooled it
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  6. Review
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  17. TOWARDS THE DEVELOPMENT OF NOVEL THERAPEUTICS FOR PERIPHERAL ARTERY DISEASE.Transactions of the American Clinical and Climatological Association · 2016
    Review
  18. Article
  19. Article
  20. Th17 Cell Plasticity and Functions in Cancer Immunity.BioMed research international · 2015
    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 3 institutions in 2 countries.

Karolien CastermansAngiogenesis Laboratory, School for Oncology and Developmental Biology, Department of Pathology, Maastricht University and University Hospital, Maastricht, The Netherlands.
Sebastien P Tabruyn
Rong Zeng
Judy R van Beijnum
Cheryl Eppolito
Warren J Leonard
Protul A Shrikant
Arjan W Griffioen
Maastricht University · NLNational Heart Lung and Blood Institute · USRoswell Park Comprehensive Cancer Center · US

Funding

IL-2 Family Cytokines and their Receptors-- Biology of the IL-21 systemZIAHL005408 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI LEONARD, WARREN J · 2009 to 2025
$23.7M
IL-2 Family Cytokines and their Receptors-- Biology of the IL-21 systemZ01HL005408 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI LEONARD, WARREN J · 2008 to 2008
$668k
6 · The paper itself

Abstract

Interleukin-21 (IL-21) is a recently described immunoregulatory cytokine. It has been identified as a very potent immunotherapeutic agent in several cancer types in animal models, and clinical studies are ongoing. IL-21 belongs to the type I cytokine family of which other members, ie, IL-2, IL-15, and IL-4, have been shown to exert activities on vascular endothelial cells (ECs). We hypothesized that IL-21, in addition to inducing the antitumor immune response, also inhibits tumor angiogenesis. In vitro experiments showed a decrease of proliferation and sprouting of activated ECs after IL-21 treatment. We found that the IL-21 receptor is expressed on vascular ECs. Furthermore, in vivo studies in the chorioallantoic membrane of the chick embryo and in mouse tumors demonstrated that IL-21 treatment disturbs vessel architecture and negatively affects vessel outgrowth. Our results also confirm the earlier suggested angiostatic potential of IL-2 in vitro and in vivo. The angiostatic effect of IL-21 is confirmed by the decrease in expression of angiogenesis-related genes. Interestingly, IL-21 treatment of ECs leads to a decrease of Stat3 phosphorylation. Our research shows that IL-21 is a very powerful antitumor compound that combines the induction of an effective antitumor immune response with inhibition of tumor angiogenesis.

Indexed as

Angiogenesis InhibitorsAnimalsAntineoplastic AgentsAortaCell LineCell Line, TumorCell ProliferationChick EmbryoEndothelial CellsEndothelium, VascularHumansInterleukin-21InterleukinsMiceNeovascularization, PathologicNeovascularization, PhysiologicAngiogenesis InhibitorsAntineoplastic AgentsInterleukin-21InterleukinsReceptors, Interleukin-21STAT3 Transcription Factor

Identifiers

PMID18515660
PMCPMC6561391
OpenAlexW2042537813

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.