Evidence map›Paper›PMID 20980681›Full record

ArticleBlood2011

Angiostatic and chemotactic activities of the CXC chemokine CXCL4L1 (platelet factor-4 variant) are mediated by CXCR3.

Sofie Struyf, Laura Salogni, Marie D Burdick, Jo Vandercappellen, Mieke Gouwy, Sam Noppen, Paul Proost, Ghislain Opdenakker, Marc Parmentier, Craig Gerard and 3 more

Abstract read
In one paragraph

Article in Blood, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

53 citing papers in PubMed, 106 citations in OpenAlex.

  1. Trial
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  3. Atypical chemokine receptors in the immune system.Nature reviews. Immunology · 2024
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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

13 authors at 6 institutions in 3 countries.

Sofie StruyfRega Institute, K.U. Leuven, Leuven, Belgium.
Laura Salogni
Marie D Burdick
Jo Vandercappellen
Mieke Gouwy
Sam Noppen
Paul Proost
Ghislain Opdenakker
Marc Parmentier
Craig Gerard
Silvano Sozzani
Robert M Strieter
Jo Van Damme
KU Leuven · BERega Institute for Medical Research · BEUniversity of Brescia · ITUniversity of Virginia · USBoston Children's Museum · USUniversité Libre de Bruxelles · BE

Funding

UCLA SPORE IN LUNG CANCERP50CA090388 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI DUBINETT, STEVEN M. · 2001 to 2008
$13.0M
CXC Chemokines in CancerR01CA087879 · NCI · UNIVERSITY OF VIRGINIA · PI STRIETER, ROBERT M · 2000 to 2010
$3.4M
Chemokines and Fibrocytes in Acute Lung InjuryR01HL066027 · NHLBI · UNIVERSITY OF VIRGINIA · PI STRIETER, ROBERT M · 2001 to 2009
$3.2M
NCI NIH HHS CA87879NCI NIH HHS P50 CA090388NCI NIH HHS P50CA90388NCI NIH HHS R01 CA087879NHLBI NIH HHS HL66027NHLBI NIH HHS R01 HL066027
6 · The paper itself

Abstract

We investigated possible cellular receptors for the human CXC chemokine platelet factor-4 variant/CXCL4L1, a potent inhibitor of angiogenesis. We found that CXCL4L1 has lower affinity for heparin and chondroitin sulfate-E than platelet factor-4 (CXCL4) and showed that CXCL10 and CXCL4L1 could displace each other on microvascular endothelial cells. Labeled CXCL4L1 also bound to CXCR3A- and CXCR3B-transfectants and was displaced by CXCL4L1, CXCL4, and CXCL10. The CXCL4L1 anti-angiogenic activity was blocked by anti-CXCR3 antibodies (Abs) in the Matrigel and cornea micropocket assays. CXCL4L1 application in CXCR3(-/-) or in wild-type mice treated with neutralizing anti-CXCR3 Abs, resulted in reduced inhibitory activity of CXCL4L1 on tumor growth and vascularization of Lewis lung carcinoma. Furthermore, CXCL4L1 and CXCL4 chemoattracted activated T cells, human natural killer cells, and human immature dendritic cells (DCs). Migration of DCs toward CXCL4 and CXCL4L1 was desensitized by preincubation with CXCL10 and CXCL11, inhibited by pertussis toxin, and neutralized by anti-CXCR3 Abs. Chemotaxis of T cells, natural killer cells, and DCs is likely to contribute to the antitumoral action. However, the in vivo data indicate that the angiostatic property of CXCL4L1 is equally important in retarding tumor growth. Thus, both CXCR3A and CXCR3B are implicated in the chemotactic and vascular effects of CXCL4L1.

Indexed as

Angiogenesis InhibitorsAnimalsAntineoplastic AgentsChemotactic FactorsChemotaxis, LeukocyteDendritic CellsEndothelial CellsHumansMiceMice, Inbred C57BLNeoplasms, ExperimentalPlatelet Factor 4RatsReceptors, CXCR3TransfectionXenograft Model Antitumor AssaysAngiogenesis InhibitorsAntineoplastic AgentsChemotactic FactorsCXCR3 protein, humanPF4V1 protein, humanPlatelet Factor 4Receptors, CXCR3

Identifiers

PMID20980681
PMCPMC3031477
OpenAlexW1983634321

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.