Evidence map›Paper›PMID 30796968›Full record

ReviewCancer letters2019

Cathepsin B: A sellsword of cancer progression.

Olja Mijanović, Ana Branković, Alexander N Panin, Solomiia Savchuk, Peter Timashev, Ilya Ulasov, Maciej S Lesniak

Open access · greenAbstract readReview
In one paragraph

Review in Cancer letters, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 84 papers.

0numbers the graph read from it
0cells of the map it votes in
84citing papers in PubMed
6.1field-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

84 citing papers in PubMed, 196 citations in OpenAlex.

  1. Dual-target carbonic anhydrase inhibitors in cancer therapy: progress, challenges, and opportunities.Medicinal chemistry research : an international journal for rapid communications on design and mechanisms of action of biologically active agents · 2026
    Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Review
  13. Article
  14. Redirecting the Peptide Cleavage Causes Protease Inactivation.Angewandte Chemie (International ed. in English) · 2025
    Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

24 more citing papers are in PubMed but not listed here.

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 5 institutions in 4 countries.

Olja MijanovićInstitute of Regenerative Medicine, Sechenov First Moscow State Medical University, Moscow, 119991, Russia.
Ana BrankovićDepartment of Forensics, Academy of Criminalistic and Police Studies, Belgrade, Serbia.
Alexander N PaninMoscow State University of Food Production, 11, Volokolamskoe Shosse, Moscow, 125080, Russia.
Solomiia SavchukThe University of Illinois at Chicago (UIC), Chicago, IL, USA; Northwestren University, Chicago, IL, 60611, USA.
Peter TimashevInstitute of Regenerative Medicine, Sechenov First Moscow State Medical University, Moscow, 119991, Russia.
Ilya UlasovInstitute of Regenerative Medicine, Sechenov First Moscow State Medical University, Moscow, 119991, Russia.
Maciej S LesniakThe University of Illinois at Chicago (UIC), Chicago, IL, USA; Northwestren University, Chicago, IL, 60611, USA. Electronic address: maciej.lesniak@northwestern.edu.
Sechenov University · RUMinistry of Interior of the Republic of Serbia · RSMoscow State University of Food Production · RUNorthwestern University · USNorthwest University · US

Funding

STINGing GBM: A First-in- Man Clinical Trial in Surgical Resectable Recurrent GBMP50CA221747 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Pouya Jamshidi · 2018 to 2026
$21.4M
Therapeutic Targeting of Malignant Glioma Stem CellsR35CA197725 · NCI · UNIVERSITY OF CHICAGO · PI LESNIAK, MACIEJ S · 2015 to 2021
$6.2M
NCI NIH HHS P50 CA221747NCI NIH HHS R35 CA197725
6 · The paper itself

Abstract

Clinical, biochemical and molecular biology studies have identified lysosome-encapsulated cellular proteases as critical risk factors for cancer progression. Cathepsins represent a group of such proteases aimed at maintenance of cellular homeostasis. Nevertheless, recent reports suggest that Cathepsin B executes other cellular programs such as controlling tumor growth, migration, invasion, angiogenesis, and metastases development. In fact, elevated levels of Cathepsins are found under different pathological conditions including inflammation, infection, neurodegenerative disease, and cancer. Furthermore, the discovery of Cathepsin B secretion and function as an extracellular matrix protein has broadened our appreciation for the impact of Cathepsin B on cancer progression. Underneath a façade of an intracellular protease with limited therapeutic potential hides a central role of cathepsins in extracellular functions. Moreover, this role is incredibly diverse from one condition to the next - from driving caspase-dependent apoptosis to facilitating tumor neovascularization and metastasis. Here we discuss the role of Cathepsin B in the oncogenic process and perspective the use of Cathepsin B for diagnostic and therapeutic applications.

Indexed as

AnimalsAntineoplastic AgentsApoptosisAutophagyBiomarkers, TumorCathepsin BCell MovementHumansNeoplasm InvasivenessNeoplasmsProtease InhibitorsRNAi TherapeuticsSignal TransductionAntineoplastic AgentsBiomarkers, TumorCathepsin BCTSB protein, humanProtease InhibitorsAutophagyCathepsin BMigrationTumor

Identifiers

PMID30796968
PMCPMC6488514
OpenAlexW2916664436

What OpenQuestion holds

Textmetadata
LicenceTDM
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.