Evidence map›Paper›PMID 27548722›Full record

ArticlePloS one2016

The Proprotein Convertase Furin Contributes to Rhabdomyosarcoma Malignancy by Promoting Vascularization, Migration and Invasion.

Patricia Jaaks, Valentina D'Alessandro, Nicole Grob, Sina Büel, Katarina Hajdin, Beat W Schäfer, Michele Bernasconi

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.5field-weighted citation impact, top 16% 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

13 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Article
  3. Prodomain processing controls BMP-10 bioactivity and targeting to fibrillin-1 in latent conformation.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
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  5. Inhibition of proprotein convertases activity results in repressed stemness and invasiveness of cancer stem cells in gastric cancer.Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association · 2024
    Article
  6. Article
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  8. Review
  9. miR-133a Replacement Attenuates Thoracic Aortic Aneurysm in Mice.Journal of the American Heart Association · 2021
    Article
  10. Article
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  12. Review
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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

7 authors at 1 institution in 1 country.

Patricia JaaksDepartment of Oncology, University Children's Hospital Zurich, Zurich, Switzerland.
Valentina D'AlessandroDepartment of Oncology, University Children's Hospital Zurich, Zurich, Switzerland.
Nicole GrobDepartment of Oncology, University Children's Hospital Zurich, Zurich, Switzerland.
Sina BüelDepartment of Oncology, University Children's Hospital Zurich, Zurich, Switzerland.
Katarina HajdinDepartment of Oncology, University Children's Hospital Zurich, Zurich, Switzerland.
Beat W SchäferDepartment of Oncology, University Children's Hospital Zurich, Zurich, Switzerland.
Michele BernasconiDepartment of Oncology, University Children's Hospital Zurich, Zurich, Switzerland.
University Children's Hospital Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The proprotein convertase (PC) furin cleaves precursor proteins, an important step in the activation of many cancer-associated proteins. Substrates of furin and furin-like PCs play a role in proliferation, metastasis and invasion. Some of them are involved in the progression of the pediatric soft tissue sarcoma rhabdomyosarcoma (RMS). In this study, we show that PCs, and in particular furin, are expressed in RMS cell lines. To investigate the functional role of furin, we generated RMS cell lines with modulated furin activity. Silencing or stable inhibition of furin delayed tumor growth in Rh30 and RD xenografts in vivo, and was correlated with lower microvessel density. Reduced furin activity also decreased migration and invasion abilities in vitro, and inhibition of furin in RMS cells diminished processing of IGF1R, VEGF-C, PDGF-B and MT1-MMP, leading to lower levels of mature proteins. Furthermore, we found that furin activity is required for proper IGF signaling in RMS cells, as furin silencing resulted in reduced phosphorylation of Akt upon IGF1 stimulation. Taken together, our results suggest that furin plays an important role in the malignant phenotype of RMS cells by activating proteins involved in tumor growth and vascularization, metastasis and invasion.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsCell Line, TumorCell MovementFurinHumansInsulin-Like Growth Factor IMatrix Metalloproteinase 14MiceMice, Inbred NODMice, SCIDNeoplasm InvasivenessNeoplasm TransplantationNeovascularization, PathologicPhosphorylationProto-Oncogene Proteins c-aktFurinFURIN protein, humanIGF1 protein, humanIGF1R protein, humanInsulin-Like Growth Factor IMatrix Metalloproteinase 14MMP14 protein, humanProto-Oncogene Proteins c-aktProto-Oncogene Proteins c-sisReceptor, IGF Type 1Receptors, SomatomedinRNA, Small InterferingVascular Endothelial Growth Factor CVEGFC protein, human

Identifiers

PMID27548722
PMCPMC4993484
OpenAlexW2511054234

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.