Evidence map›Paper›PMID 42797398›Full record

ReviewPharmaceuticals (Basel, Switzerland)2026

PROTAC-Based Strategies in Neurodegenerative Diseases: Challenges and Perspectives.

Pasquale Degennaro, Imane Ghafir El Idrissi, Rosa Purgatorio, Annalisa Fanizzi, Mariagrazia Rullo, Leonardo Pisani, Eleonora Macchia, Luisa Torsi, Angela Stefanachi, Francesco Leonetti

Abstract readReview
In one paragraph

Review in Pharmaceuticals (Basel, Switzerland), 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

10 authors.

Pasquale DegennaroDepartment of Pharmacy and Pharmaceutical Science, University of Bari Aldo Moro, 70125 Bari, Italy.
Imane Ghafir El IdrissiDepartment of Pharmacy and Pharmaceutical Science, University of Bari Aldo Moro, 70125 Bari, Italy.ORCID 0000-0001-6388-6265
Rosa PurgatorioDepartment of Pharmacy and Pharmaceutical Science, University of Bari Aldo Moro, 70125 Bari, Italy.ORCID 0000-0003-1002-5087
Annalisa FanizziDepartment of Pharmacy and Pharmaceutical Science, University of Bari Aldo Moro, 70125 Bari, Italy.
Mariagrazia RulloDepartment of Pharmacy and Pharmaceutical Science, University of Bari Aldo Moro, 70125 Bari, Italy.ORCID 0000-0001-5304-6764
Leonardo PisaniDepartment of Pharmacy and Pharmaceutical Science, University of Bari Aldo Moro, 70125 Bari, Italy.ORCID 0000-0002-4198-3897
Eleonora MacchiaDepartment of Pharmacy and Pharmaceutical Science, University of Bari Aldo Moro, 70125 Bari, Italy.
Luisa TorsiDepartment of Chemistry, University of Bari Aldo Moro, 70125 Bari, Italy.
Angela StefanachiDepartment of Pharmacy and Pharmaceutical Science, University of Bari Aldo Moro, 70125 Bari, Italy.ORCID 0000-0002-9430-7972
Francesco LeonettiDepartment of Pharmacy and Pharmaceutical Science, University of Bari Aldo Moro, 70125 Bari, Italy.ORCID 0000-0003-2043-7464

Funding

Ministry of Health Italian network of excellence for advanced diagnosis (INNOVA), Ministero della Salute -code PNC-E3-2022-23683266 PNC-HLS-DA, CUP: C43C22001630001
6 · The paper itself

Abstract

Proteolysis-Targeting Chimeras (PROTACs) are heterobifunctional molecules that induce the selective degradation of a protein of interest by recruiting an E3 ubiquitin ligase, thereby triggering ubiquitination and proteasomal clearance. As part of the broader targeted protein degradation (TPD) paradigm, PROTACs offer a powerful strategy to eliminate pathogenic proteins that are difficult to modulate with traditional occupancy-based inhibitors. However, their clinical translation is often limited by poor aqueous solubility, suboptimal cellular permeability, and off-target effects. Notably, some PROTACs retain potent biological activity despite limited membrane permeability, owing to their catalytic mechanism of action, which allows even a small number of molecules reaching the target site to drive substantial protein degradation and produce important pharmacological effects. Growing evidence supports the application of PROTAC-based approaches in neurodegenerative diseases, where the selective removal of toxic or misfolded proteins is particularly attractive. This review summarizes recent advances in chemical protein degradation strategies for neurodegenerative disorders and highlights potential future perspectives of multifunctional PROTACs for therapeutic development.

Indexed as

multi-target strategiesneurodegenerative diseasesProteolysis-Targeting Chimeras (PROTACs)targeted protein degradation (TPD)

Identifiers

PMID42797398
PMCPMC13610033

What OpenQuestion holds

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Registered trials

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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.