Evidence map›Paper›PMID 31382462›Full record

ArticleCancers2019

Coagulation Factor Xa Promotes Solid Tumor Growth, Experimental Metastasis and Endothelial Cell Activation.

Maximiliano Arce, Mauricio P Pinto, Macarena Galleguillos, Catalina Muñoz, Soledad Lange, Carolina Ramirez, Rafaela Erices, Pamela Gonzalez, Ethel Velasquez, Fabián Tempio and 20 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 14% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

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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

30 authors at 10 institutions in 3 countries.

Maximiliano ArceFaculty of Biological Sciences, Pontificia Universidad Católica de Chile, Santiago 8331150, Chile.
Mauricio P PintoFaculty of Medicine, Pontificia Universidad Católica de Chile, Santiago 8331150, Chile.ORCID 0000-0003-2484-8033
Macarena GalleguillosFaculty of Biological Sciences, Pontificia Universidad Católica de Chile, Santiago 8331150, Chile.
Catalina MuñozFaculty of Biological Sciences, Pontificia Universidad Católica de Chile, Santiago 8331150, Chile.
Soledad LangeFaculty of Biological Sciences, Pontificia Universidad Católica de Chile, Santiago 8331150, Chile.
Carolina RamirezFaculty of Biological Sciences, Pontificia Universidad Católica de Chile, Santiago 8331150, Chile.
Rafaela EricesFaculty of Biological Sciences, Pontificia Universidad Católica de Chile, Santiago 8331150, Chile.ORCID 0000-0002-8499-8968
Pamela GonzalezFaculty of Biological Sciences, Pontificia Universidad Católica de Chile, Santiago 8331150, Chile.
Ethel VelasquezFaculty of Biological Sciences, Pontificia Universidad Católica de Chile, Santiago 8331150, Chile.ORCID 0000-0002-8768-9458
Fabián TempioInstitute of Biomedical Sciences, Faculty of Medicine, University de Chile, Santiago 8380453, Chile.
Mercedes N LopezInstitute of Biomedical Sciences, Faculty of Medicine, University de Chile, Santiago 8380453, Chile.
Flavio Salazar-OnfrayInstitute of Biomedical Sciences, Faculty of Medicine, University de Chile, Santiago 8380453, Chile.
Kelly CautivoFaculty of Biological Sciences, Pontificia Universidad Católica de Chile, Santiago 8331150, Chile.ORCID 0000-0003-4434-2814
Alexis M KalergisFaculty of Biological Sciences, Pontificia Universidad Católica de Chile, Santiago 8331150, Chile.
Sebastián CruzLaboratory of Immunoncology, Fundación Ciencia & Vida, Santiago, Chile.
Álvaro LladserMillennium Institute on Immunology and Immunotherapy, Santiago 8331150, Chile.
Lorena Lobos-GonzálezAdvanced Center for Chronic Diseases (ACCDiS), Santiago, Chile.
Guillermo ValenzuelaFaculty of Medicine, Pontificia Universidad Católica de Chile, Santiago 8331150, Chile.
Nixa OlivaresFaculty of Medicine, Pontificia Universidad Católica de Chile, Santiago 8331150, Chile.ORCID 0000-0001-8702-0052
Claudia SáezFaculty of Medicine, Pontificia Universidad Católica de Chile, Santiago 8331150, Chile.
Tania KoningImmunology Institute, Faculty of Medicine, Universidad Austral de Chile, Valdivia 5110566, Chile.
Fabiola A SánchezImmunology Institute, Faculty of Medicine, Universidad Austral de Chile, Valdivia 5110566, Chile.
Patricia FuenzalidaFaculty of Biological Sciences, Pontificia Universidad Católica de Chile, Santiago 8331150, Chile.
Alejandro GodoyFaculty of Biological Sciences, Pontificia Universidad Católica de Chile, Santiago 8331150, Chile.
Pamela Contreras OrellanaAdvanced Center for Chronic Diseases (ACCDiS), Santiago, Chile.
Lisette LeytonAdvanced Center for Chronic Diseases (ACCDiS), Santiago, Chile.ORCID 0000-0001-9690-9638
Roberta LuganoDepartment of Immunology, Genetics and Pathology, Rudbeck Laboratory, Uppsala University, 751 85 Uppsala, Sweden.
Anna DimbergDepartment of Immunology, Genetics and Pathology, Rudbeck Laboratory, Uppsala University, 751 85 Uppsala, Sweden.
Andrew F G QuestAdvanced Center for Chronic Diseases (ACCDiS), Santiago, Chile.ORCID 0000-0001-8755-1590
Gareth I OwenFaculty of Biological Sciences, Pontificia Universidad Católica de Chile, Santiago 8331150, Chile. gowen@bio.puc.cl.ORCID 0000-0003-3807-6054
Pontificia Universidad Católica de Chile · CLAdvanced Center for Chronic Diseases · CLAustral University of Chile · CLFundación Ciencia and Vida · CLMillennium Institute on Immunology and Immunotherapy · CLUppsala University · SERoswell Park Comprehensive Cancer Center · USUniversidad del Desarrollo · CLUniversidad Mayor · CLUniversity of Chile · CL

Funding

Fondo Nacional de Desarrollo Científico, Tecnológico y de Innovación Tecnológica 1140970
6 · The paper itself

Abstract

Hypercoagulable state is linked to cancer progression; however, the precise role of the coagulation cascade is poorly described. Herein, we examined the contribution of a hypercoagulative state through the administration of intravenous Coagulation Factor Xa (FXa), on the growth of solid human tumors and the experimental metastasis of the B16F10 melanoma in mouse models. FXa increased solid tumor volume and lung, liver, kidney and lymph node metastasis of tail-vein injected B16F10 cells. Concentrating on the metastasis model, upon coadministration of the anticoagulant Dalteparin, lung metastasis was significantly reduced, and no metastasis was observed in other organs. FXa did not directly alter proliferation, migration or invasion of cancer cells in vitro. Alternatively, FXa upon endothelial cells promoted cytoskeleton contraction, disrupted membrane VE-Cadherin pattern, heightened endothelial-hyperpermeability, increased inflammatory adhesion molecules and enhanced B16F10 adhesion under flow conditions. Microarray analysis of endothelial cells treated with FXa demonstrated elevated expression of inflammatory transcripts. Accordingly, FXa treatment increased immune cell infiltration in mouse lungs, an effect reduced by dalteparin. Taken together, our results suggest that FXa increases B16F10 metastasis via endothelial cell activation and enhanced cancer cell-endothelium adhesion advocating that the coagulation system is not merely a bystander in the process of cancer metastasis.

Indexed as

blood coagulationcancerinflammationmelanomametastasisvascular endothelium

Identifiers

PMID31382462
PMCPMC6721564
OpenAlexW2966329577

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.