Evidence map›Paper›PMID 38891048›Full record

ReviewCells2024

Unveiling the Roles of Cysteine Proteinases F and W: From Structure to Pathological Implications and Therapeutic Targets.

Kristina Zdravkova, Olja Mijanovic, Ana Brankovic, Polina M Ilicheva, Aleksandra Jakovleva, Jelena Karanovic, Milena Pualic, Dusan Pualic, Aleksandr A Rubel, Lyudmila V Savvateeva and 2 more

Abstract readReview
In one paragraph

Review in Cells, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. 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

12 authors.

Kristina ZdravkovaAD Alkaloid Skopje, Boulevard Alexander the Great 12, 1000 Skopje, North Macedonia.ORCID 0009-0001-5825-5570
Olja MijanovicDia-M, LCC, 7 b.3 Magadanskaya Str., 129345 Moscow, Russia.
Ana BrankovicDepartment of Forensic Sciences, Faculty of Forensic Sciences and Engineering, University of Criminal Investigation and Police Studies, Cara Dusana 196, 11000 Belgrade, Serbia.ORCID 0000-0002-3197-118X
Polina M IlichevaInstitute of Chemistry, Saratov State University, Astrakhanskaya Street 83, 410012 Saratov, Russia.ORCID 0000-0002-5825-0032
Aleksandra JakovlevaHoxLife Science GmbH, Gutleutstraße 169-171, 60327 Frankfurt am Main, Germany.ORCID 0009-0008-0494-9674
Jelena KaranovicLaboratory for Molecular Biology, Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Vojvode Stepe 444A, 11000 Belgrade, Serbia.
Milena PualicInstitute Cardiovascular Diseases Dedinje, Heroja Milana Tepica 1, 11000 Belgrade, Serbia.
Dusan PualicMilitary Medical Academy, Crnotravska 17, 11000 Belgrade, Serbia.
Aleksandr A RubelLaboratory of Amyloid Biology, St. Petersburg State University, 199034 St. Petersburg, Russia.ORCID 0000-0001-6203-2006
Lyudmila V SavvateevaInstitute of Translational Medicine and Biotechnology, Sechenov First Moscow State Medical University, 119991 Moscow, Russia.
Alessandro ParodiResearch Center for Translational Medicine, Sirius University of Science and Technology, 354340 Sochi, Russia.ORCID 0000-0003-0985-6545
Andrey A ZamyatninFaculty of Bioengineering and Bioinformatics, Lomonosov Moscow State University, 119234 Moscow, Russia.ORCID 0000-0002-3046-4565

Funding

Russian Science Foundation 21-75-30020
6 · The paper itself

Abstract

Cysteine cathepsins F and W are members of the papain-like cysteine protease family, which have distinct structural features and functional roles in various physiological and pathological processes. This review provides a comprehensive overview of the current understanding of the structure, biological functions, and pathological implications of cathepsins F and W. Beginning with an introduction to these proteases, we delve into their structural characteristics and elucidate their unique features that dictate their enzymatic activities and substrate specificity. We also explore the intricate involvement of cathepsins F and W in malignancies, highlighting their role as potential biomarkers and therapeutic targets in cancer progression. Furthermore, we discuss the emerging roles of these enzymes in immune response modulation and neurological disorders, shedding light on their implications in autoimmune and neurodegenerative diseases. Finally, we review the landscape of inhibitors targeting these proteases, highlighting their therapeutic potential and challenges in clinical translation. This review brings together the diverse facets of cysteine cathepsins F and W, providing insights into their roles in health and disease and guiding future investigations for therapeutic advances.

Indexed as

Cathepsin FAnimalsCathepsinsCysteine ProteasesHumansNeoplasmsSubstrate SpecificityCathepsin FCathepsinsCysteine Proteasescysteine cathepsinsinhibitorspathologytherapy

Identifiers

PMID38891048
PMCPMC11171618

What OpenQuestion holds

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LicenceCC BY
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.