Evidence map›Paper›PMID 41787612›Full record

ReviewMini reviews in medicinal chemistry2026

New Therapeutic Options Against Clinically Relevant Proteases in Cancer Progression.

Anastasia O Syrocheva, Darya S Volkova, Evgenya R Denisova, Valeria V Streltsova, Polina S Marukhina, Alessandro Parodi, Andrey A Zamyatnin

Abstract readReview
PubMed Publisher
In one paragraph

Review in Mini reviews in medicinal chemistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Anastasia O SyrochevaResearch Center for Translational Medicine, Sirius University of Science and Technology, 354340, Sochi, Russia.ORCID 0009-0008-5035-8445
Darya S VolkovaResearch Center for Translational Medicine, Sirius University of Science and Technology, 354340, Sochi, Russia.
Evgenya R DenisovaResearch Center for Translational Medicine, Sirius University of Science and Technology, 354340, Sochi, Russia.
Valeria V StreltsovaResearch Center for Translational Medicine, Sirius University of Science and Technology, 354340, Sochi, Russia.
Polina S MarukhinaResearch Center for Translational Medicine, Sirius University of Science and Technology, 354340, Sochi, Russia.
Alessandro ParodiResearch Center for Translational Medicine, Sirius University of Science and Technology, 354340, Sochi, Russia.
Andrey A ZamyatninFaculty of Bioengineering and Bioinformatics, Lomonosov Moscow State University, 119234, Moscow, Russia.

Funding

state program of the "Sirius" Federal Territory "Scientific and technological development of the "Sirius" Federal Territory" 3-03
6 · The paper itself

Abstract

Proteases are key regulators in cancer progression and metastasis, representing promising therapeutic targets. This review underscores the critical role of diverse proteases-encompassing cell surface ectoproteases, extracellular proteases, and intracellular proteases-in tumor biology, with a focus on the most significant and clinically relevant ones. Their overexpression in tumors reflects their importance in cancer development, invasion, and drug resistance. Emerging research has unveiled novel strategies to target proteases for cancer therapy, offering hope for improved treatment outcomes. However, challenges, such as selectivity, drug delivery, and toxicity remain significant hurdles to overcome. This article discusses current advancements, challenges, and future opportunities in targeting proteases for cancer therapy.

Indexed as

Antineoplastic AgentsNeoplasmsPeptide HydrolasesProtease InhibitorsAnimalsDisease ProgressionHumansAntineoplastic AgentsPeptide HydrolasesProtease InhibitorsCancercathepsinsectoproteasesextracellular proteasesmatrix metalloproteinasesoncogenesisprotease inhibitorsproteasessecreted proteasestargeting drug delivery

Identifiers

What OpenQuestion holds

Textmetadata
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.