Evidence map›Paper›PMID 35203374›Full record

ReviewCells2022

Antiplatelet Agents Affecting GPCR Signaling Implicated in Tumor Metastasis.

Gianenrico Rovati, Annalisa Contursi, Annalisa Bruno, Stefania Tacconelli, Patrizia Ballerini, Paola Patrignani

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 30% 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

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Article
  3. Exploiting the 2-(1,3,4,9-tetrahydropyrano[3,4-Journal of medicinal chemistry · 2025
    Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. 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

6 authors at 2 institutions in 1 country.

Gianenrico RovatiDepartment of Pharmaceutical Sciences, University of Milan, 20122 Milan, Italy.ORCID 0000-0002-8788-9783
Annalisa ContursiLaboratory of Systems Pharmacology and Translational Therapies, Center for Advanced Studies and Technology (CAST), School of Medicine, "G. d'Annunzio" University, 66100 Chieti, Italy.
Annalisa BrunoLaboratory of Systems Pharmacology and Translational Therapies, Center for Advanced Studies and Technology (CAST), School of Medicine, "G. d'Annunzio" University, 66100 Chieti, Italy.ORCID 0000-0002-6167-7141
Stefania TacconelliLaboratory of Systems Pharmacology and Translational Therapies, Center for Advanced Studies and Technology (CAST), School of Medicine, "G. d'Annunzio" University, 66100 Chieti, Italy.
Patrizia BalleriniLaboratory of Systems Pharmacology and Translational Therapies, Center for Advanced Studies and Technology (CAST), School of Medicine, "G. d'Annunzio" University, 66100 Chieti, Italy.
Paola PatrignaniLaboratory of Systems Pharmacology and Translational Therapies, Center for Advanced Studies and Technology (CAST), School of Medicine, "G. d'Annunzio" University, 66100 Chieti, Italy.ORCID 0000-0003-1419-2691
University of Chieti-Pescara · ITUniversity of Milan · IT

Funding

Cancer Research UK 24991
6 · The paper itself

Abstract

Metastasis requires that cancer cells survive in the circulation, colonize distant organs, and grow. Despite platelets being central contributors to hemostasis, leukocyte trafficking during inflammation, and vessel stability maintenance, there is significant evidence to support their essential role in supporting metastasis through different mechanisms. In addition to their direct interaction with cancer cells, thus forming heteroaggregates such as leukocytes, platelets release molecules that are necessary to promote a disseminating phenotype in cancer cells via the induction of an epithelial-mesenchymal-like transition. Therefore, agents that affect platelet activation can potentially restrain these prometastatic mechanisms. Although the primary adhesion of platelets to cancer cells is mainly independent of G protein-mediated signaling, soluble mediators released from platelets, such as ADP, thromboxane (TX) A

Indexed as

NeoplasmsPlatelet Aggregation InhibitorsBlood PlateletsHumansPlatelet ActivationReceptors, G-Protein-CoupledThromboxane A2Platelet Aggregation InhibitorsReceptors, G-Protein-CoupledThromboxane A2antithrombotic agentsaspirincancer metastasiscyclooxygenasesepithelial–mesenchymal transitionG protein-coupled receptorsP2Y12 antagonistsPGE2 receptor antagonistsplateletsTXA2 receptor antagonists

Identifiers

PMID35203374
PMCPMC8870128
OpenAlexW4213260752

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.