Evidence map›Paper›PMID 34198733›Full record

ReviewPharmaceutics2021

Cathepsin D-Managing the Delicate Balance.

Olja Mijanovic, Anastasiia I Petushkova, Ana Brankovic, Boris Turk, Anna B Solovieva, Angelina I Nikitkina, Sergey Bolevich, Peter S Timashev, Alessandro Parodi, Andrey A Zamyatnin

Open access · goldAbstract readReview
In one paragraph

Review in Pharmaceutics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
4.4field-weighted citation impact, top 4% 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

48 citing papers in PubMed, 81 citations in OpenAlex.

  1. Article
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  8. The miR-214-3p/Biology · 2026
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  17. Design and Preclinical Evaluation of FirstJournal of medicinal chemistry · 2025
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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

10 authors at 4 institutions in 3 countries.

Olja MijanovicInstitute for Regenerative Medicine, Sechenov First Moscow State Medical University, 119991 Moscow, Russia.
Anastasiia I PetushkovaInstitute of Molecular Medicine, Sechenov First Moscow State Medical University, 119991 Moscow, Russia.
Ana BrankovicDepartment of Forensic Engineering, University of Criminal Investigation and Police Studies, 11080 Belgrade, Serbia.
Boris TurkInstitute for Regenerative Medicine, Sechenov First Moscow State Medical University, 119991 Moscow, Russia.ORCID 0000-0002-9007-5764
Anna B SolovievaSemenov Institute of Chemical Physics, Russian Academy of Sciences, 119991 Moscow, Russia.
Angelina I NikitkinaInstitute for Regenerative Medicine, Sechenov First Moscow State Medical University, 119991 Moscow, Russia.
Sergey BolevichDepartment of Human Pathology, Sechenov University, 119991 Moscow, Russia.
Peter S TimashevInstitute for Regenerative Medicine, Sechenov First Moscow State Medical University, 119991 Moscow, Russia.ORCID 0000-0001-7773-2435
Alessandro ParodiInstitute of Molecular Medicine, Sechenov First Moscow State Medical University, 119991 Moscow, Russia.
Andrey A ZamyatninInstitute of Molecular Medicine, Sechenov First Moscow State Medical University, 119991 Moscow, Russia.ORCID 0000-0002-3046-4565
Sechenov University · RUMinistry of Interior of the Republic of Serbia · RSSemenov Institute of Chemical Physics · RUUniversity of Ljubljana · SI

Funding

Ministry of Science and Higher Education of the Russian Federation 075-15-2020-926
6 · The paper itself

Abstract

Lysosomal proteases play a crucial role in maintaining cell homeostasis. Human cathepsin D manages protein turnover degrading misfolded and aggregated proteins and favors apoptosis in the case of proteostasis disruption. However, when cathepsin D regulation is affected, it can contribute to numerous disorders. The down-regulation of human cathepsin D is associated with neurodegenerative disorders, such as neuronal ceroid lipofuscinosis. On the other hand, its excessive levels outside lysosomes and the cell membrane lead to tumor growth, migration, invasion and angiogenesis. Therefore, targeting cathepsin D could provide significant diagnostic benefits and new avenues of therapy. Herein, we provide a brief overview of cathepsin D structure, regulation, function, and its role in the progression of many diseases and the therapeutic potentialities of natural and synthetic inhibitors and activators of this protease.

Indexed as

cathepsin Ddiabetesinhibitorslysosomemalignant tumorneurodegenerative diseaseregulated cell death

Identifiers

PMID34198733
PMCPMC8229105
OpenAlexW3166118562

What OpenQuestion holds

Textmetadata
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.