Evidence map›Paper›PMID 7543496›Full record

ArticleThe Journal of clinical investigation1995

Platelet activating factor produced in vitro by Kaposi's sarcoma cells induces and sustains in vivo angiogenesis.

F Bussolino, M Arese, G Montrucchio, L Barra, L Primo, R Benelli, F Sanavio, M Aglietta, D Ghigo, M R Rola-Pleszczynski

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

29 citing papers in PubMed, 101 citations in OpenAlex.

  1. Review
  2. Physiology of chemokines in the cancer microenvironment.American journal of physiology. Cell physiology · 2023
    Review
  3. Article
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  17. Emerging roles of PAR-1 and PAFR in melanoma metastasis.Cancer microenvironment : official journal of the International Cancer Microenvironment Society · 2008
    Article
  18. G-protein coupled chemoattractant receptors and cancer.Frontiers in bioscience : a journal and virtual library · 2008
    Review
  19. Article
  20. Article
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

10 authors at 3 institutions in 1 country.

F BussolinoDipartimento di Genetica, Biologia e Chimica Medica, University of Torino, Italy.
M Arese
G Montrucchio
L Barra
L Primo
R Benelli
F Sanavio
M Aglietta
D Ghigo
M R Rola-Pleszczynski
Candiolo Cancer Institute · ITAlleanza Contro il Cancro · ITUniversity of Turin · IT

Funding

Telethon 582
6 · The paper itself

Abstract

Imbalance in the network of soluble mediators may play a pivotal role in the pathogenesis of Kaposi's sarcoma (KS). In this study, we demonstrated that KS cells grown in vitro produced and in part released platelet activating factor (PAF), a powerful lipid mediator of inflammation and cell-to-cell communication. IL-1, TNF, and thrombin enhanced the synthesis of PAF. PAF receptor mRNA and specific, high affinity binding site for PAF were present in KS cells. Nanomolar concentration of PAF stimulated the chemotaxis and chemokinesis of KS cells, endothelial cells, and vascular smooth muscle cells. The migration response to PAF was inhibited by WEB 2170, a hetrazepinoic PAF receptor antagonist. Because neoangiogenesis is essential for the growth and progression of KS and since PAF can activate vascular endothelial cells, we examined the potential role of PAF as an instrumental mediator of angiogenesis associated with KS. Conditioned medium (CM) from KS cells (KS-CM) or KS cells themselves induced angiogenesis and macrophage recruitment in a murine model in which Matrigel was injected subcutaneously. These effects were inhibited by treating mice with WEB 2170. Synthetic PAF or natural PAF extracted from plasma of patients with classical KS also induced angiogenesis, which in turn was inhibited by WEB 2170. The action of PAF was amplified by expression of other angiogenic factors and chemokines: these included basic and acidic fibroblast growth factor, placental growth factor, vascular endothelial growth factor and its specific receptor flk-1, hepatocyte growth factor, KC, and macrophage inflammatory protein-2. Treatment with WEB 2170 abolished the expression of the transcripts of these molecules within Matrigel containing KS-CM. These results indicate that PAF may cooperate with other angiogenic molecules and chemokines in inducing vascular development in KS.

Indexed as

Receptors, Cell SurfaceReceptors, G-Protein-CoupledAgedAnimalsAzepinesBase SequenceCell LineChemotaxisChoriocarcinomaCollagenCulture Media, ConditionedCytokinesDogsDrug CombinationsEndothelium, VascularFemaleAzepinesbepafantCollagenCulture Media, ConditionedCytokinesDrug CombinationsGrowth SubstancesInterleukin-1LamininmatrigelNeoplasm ProteinsO-deacetyl platelet activating factorPlatelet Activating Factorplatelet activating factor receptorPlatelet Membrane GlycoproteinsProteoglycansReceptors, Cell SurfaceReceptors, G-Protein-CoupledThrombinTriazolesTumor Necrosis Factor-alpha

Identifiers

PMID7543496
PMCPMC185282
OpenAlexW2114188952

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.