Evidence map›Paper›PMID 32365084›Full record

ArticlePloS one2020

Role of trypsin and protease-activated receptor-2 in ovarian cancer.

Kyu Kwang Kim, Rachael Turner, Negar Khazan, Arif Kodza, Aaron Jones, Rakesh K Singh, Richard G Moore

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.5field-weighted citation impact, top 9% 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

21 citing papers in PubMed, 40 citations in OpenAlex.

  1. Review
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  8. New Target(s) for RNF43 Regulation: Implications for Therapeutic Strategies.International journal of molecular sciences · 2024
    Review
  9. Article
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  11. Article
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  14. The Proteolytic Landscape of Ovarian Cancer: Applications in Nanomedicine.International journal of molecular sciences · 2022
    Review
  15. Article
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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.

Kyu Kwang KimThe Wilmot Cancer Institute at the University of Rochester Medical Center, Rochester, NY, United States of America.ORCID 0000-0002-0386-3712
Rachael TurnerThe Wilmot Cancer Institute at the University of Rochester Medical Center, Rochester, NY, United States of America.
Negar KhazanThe Wilmot Cancer Institute at the University of Rochester Medical Center, Rochester, NY, United States of America.
Arif KodzaThe Wilmot Cancer Institute at the University of Rochester Medical Center, Rochester, NY, United States of America.ORCID 0000-0003-1415-3334
Aaron JonesThe Wilmot Cancer Institute at the University of Rochester Medical Center, Rochester, NY, United States of America.
Rakesh K SinghThe Wilmot Cancer Institute at the University of Rochester Medical Center, Rochester, NY, United States of America.
Richard G MooreThe Wilmot Cancer Institute at the University of Rochester Medical Center, Rochester, NY, United States of America.
University of Rochester Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Proteases have been implicated in the tumorigenesis and aggressiveness of a variety of cancer types. In fact, proteases have proven to be very clinically useful as tumor biomarkers in the blood of patients. Proteases are typically involved in complex systems of substrates, activators, and inhibitors, thus making our ability to establish their exact function in cancer more difficult. Trypsin, perhaps the most famous of proteases, has been shown to play a role in cancer progression, but its functional role in ovarian cancer has not been much studied. PAR2, a transmembrane receptor that is known to be activated by trypsin, has been reported to be associated with ovarian cancer. Here, we found that stimulation of ovarian cancer cell lines with trypsin or PAR2 activating peptide markedly increased MAPK signaling and cell proliferation. Additionally, HE4, a WAP-family glycoprotein and ovarian cancer biomarker, was found to inhibit trypsin degradation, thereby retaining its activity. Patient data seemed to support this phenomenon, as the serum of ovarian cancer patients with high HE4 expression, revealed significantly elevated trypsin levels. These data support the hypothesis that trypsin plays a tumorigenic role in ovarian cancer, which can be mediated by its receptor PAR2, and potentiated by HE4.

Indexed as

Carcinoma, Ovarian EpithelialCell Line, TumorCell ProliferationFemaleGene Expression Regulation, NeoplasticHumansMAP Kinase Signaling SystemOvarian NeoplasmsProteolysisReceptor, PAR-2TrypsinUp-RegulationWAP Four-Disulfide Core Domain Protein 2F2RL1 protein, humanReceptor, PAR-2TrypsinWAP Four-Disulfide Core Domain Protein 2WFDC2 protein, human

Identifiers

PMID32365084
PMCPMC7197761
OpenAlexW3021920840

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.