Evidence map›Paper›PMID 36598826›Full record

ReviewIUBMB life2023

The roles of proteases in prostate cancer.

Hannu Koistinen, Ruusu-Maaria Kovanen, Morley D Hollenberg, Antoine Dufour, Evette S Radisky, Ulf-Håkan Stenman, Jyotsna Batra, Judith Clements, John D Hooper, Eleftherios Diamandis and 3 more

Open access · hybridAbstract readReview
In one paragraph

Review in IUBMB life, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
8.4field-weighted citation impact, top 2% 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

20 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. From Hypoxia to Bone: Reprogramming the Prostate Cancer Metastatic Cascade.International journal of molecular sciences · 2025
    Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Androgen Signaling in Prostate Cancer: When a Friend Turns Foe.Endocrine, metabolic & immune disorders drug targets · 2025
    Review
  13. Proteases: Role in Various Human Diseases.Current pharmaceutical biotechnology · 2025
    Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. 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

13 authors at 7 institutions in 5 countries.

Hannu KoistinenDepartment of Clinical Chemistry and Haematology, Faculty of Medicine, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.ORCID 0000-0003-0926-3109
Ruusu-Maaria KovanenDepartment of Clinical Chemistry and Haematology, Faculty of Medicine, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.ORCID 0000-0001-5817-890X
Morley D HollenbergDepartment of Physiology & Pharmacology and Department of Medicine, Cumming School of Medicine, University of Calgary, Calgary, Canada.ORCID 0000-0003-4070-8786
Antoine DufourDepartment of Physiology & Pharmacology and Department of Medicine, Cumming School of Medicine, University of Calgary, Calgary, Canada.ORCID 0000-0002-3429-4188
Evette S RadiskyDepartment of Cancer Biology, Mayo Clinic, Jacksonville, Florida, USA.ORCID 0000-0003-3121-109X
Ulf-Håkan StenmanDepartment of Clinical Chemistry and Haematology, Faculty of Medicine, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.ORCID 0000-0002-2695-3454
Jyotsna BatraSchool of Biomedical Sciences, Faculty of Health, Queensland University of Technology, Brisbane, Australia.ORCID 0000-0003-4646-6247
Judith ClementsSchool of Biomedical Sciences, Faculty of Health, Queensland University of Technology, Brisbane, Australia.ORCID 0000-0001-6026-1964
John D HooperMater Research Institute, The University of Queensland, Brisbane, Australia.ORCID 0000-0003-1054-8486
Eleftherios DiamandisDepartment of Pathology and Laboratory Medicine, Mount Sinai Hospital, Toronto, Canada.ORCID 0000-0002-1589-820X
Oliver SchillingFaculty of Medicine, Institute for Surgical Pathology, Medical Center - University of Freiburg, University of Freiburg, Freiburg, Germany.ORCID 0000-0001-7678-7653
Antti RannikkoResearch Program in Systems Oncology, Faculty of Medicine, University of Helsinki, Helsinki, Finland.ORCID 0000-0002-4261-3484
Tuomas MirttiResearch Program in Systems Oncology, Faculty of Medicine, University of Helsinki, Helsinki, Finland.ORCID 0000-0003-0455-9891
University of Helsinki · FITranslational Research Institute · AUUniversity of Calgary · CAJacksonville College · USMount Sinai Hospital · CAThe University of Queensland · AUUniversity of Freiburg · DE

Funding

Engineering tissue inhibitor of metalloproteinases-2 (TIMP-2) for triple negative breast cancer therapyR01CA258274 · NCI · MAYO CLINIC JACKSONVILLE · PI RADISKY, EVETTE S · 2021 to 2025
$1.6M
Exploiting new approaches for selective inhibition of trypsinsR01GM144393 · NIGMS · MAYO CLINIC JACKSONVILLE · PI Evette S Radisky · 2022 to 2026
$1.5M
Engineering selective inhibition of metalloproteinases by tissue inhibitors of metalloproteinases (R01 GM132100 RESUB - *TIMPs)R01GM132100 · NIGMS · MAYO CLINIC JACKSONVILLE · PI RADISKY, EVETTE S · 2020 to 2023
$1.3M
NCI NIH HHS R01 CA258274NIGMS NIH HHS R01 GM132100NIGMS NIH HHS R01 GM144393NIH HHS R01 CA258274NIH HHS R01 GM132100NIH HHS R01GM144393
6 · The paper itself

Abstract

Since the proposition of the pro-invasive activity of proteolytic enzymes over 70 years ago, several roles for proteases in cancer progression have been established. About half of the 473 active human proteases are expressed in the prostate and many of the most well-characterized members of this enzyme family are regulated by androgens, hormones essential for development of prostate cancer. Most notably, several kallikrein-related peptidases, including KLK3 (prostate-specific antigen, PSA), the most well-known prostate cancer marker, and type II transmembrane serine proteases, such as TMPRSS2 and matriptase, have been extensively studied and found to promote prostate cancer progression. Recent findings also suggest a critical role for proteases in the development of advanced and aggressive castration-resistant prostate cancer (CRPC). Perhaps the most intriguing evidence for this role comes from studies showing that the protease-activated transmembrane proteins, Notch and CDCP1, are associated with the development of CRPC. Here, we review the roles of proteases in prostate cancer, with a special focus on their regulation by androgens.

Indexed as

Peptide HydrolasesProstatic NeoplasmsAnimalsBiomarkers, TumorHumansProtein Kinase InhibitorsBiomarkers, TumorPeptide HydrolasesProtein Kinase Inhibitorsandrogenandrogen receptorARCDCP1CUB domain-containing protein 1FAPfibroblast activation proteinhepsinkallikrein-related peptidasesKLKmatriptasematrix metalloproteinaseMMPNotchPARpeptidasesprostate cancerprotease-activated receptorproteasesTMPRSS2trypsinuPAurokinase-type plasminogen activator

Identifiers

PMID36598826
PMCPMC10159896
OpenAlexW4313543655

What OpenQuestion holds

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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.