Evidence map›Paper›PMID 38786097›Full record

ArticleCells2024

A Proteomic Approach Identified TFEB as a Key Player in the Protective Action of Novel CB2R Bitopic Ligand FD22a against the Deleterious Effects Induced by β-Amyloid in Glial Cells.

Beatrice Polini, Lorenzo Zallocco, Francesca Gado, Rebecca Ferrisi, Caterina Ricardi, Mariachiara Zuccarini, Vittoria Carnicelli, Clementina Manera, Maurizio Ronci, Antonio Lucacchini and 3 more

Abstract read
In one paragraph

Article in Cells, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
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  7. Review
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

13 authors.

Beatrice PoliniDepartment of Pathology, University of Pisa, 56100 Pisa, Italy.ORCID 0000-0002-2664-6091
Lorenzo ZalloccoDepartment of Translational Research and New Technologies in Medicine and Surgery, University of Pisa, 56126 Pisa, Italy.ORCID 0000-0001-6385-4116
Francesca GadoDepartment of Pharmaceutical Sciences, University of Milan, 20133 Milano, Italy.ORCID 0000-0003-2971-0834
Rebecca FerrisiDepartment of Pharmaceutical Sciences, University of Milan, 20133 Milano, Italy.
Caterina RicardiDepartment of Pathology, University of Pisa, 56100 Pisa, Italy.
Mariachiara ZuccariniDepartment of Medical, Oral and Biotechnological Sciences, University G. D'Annunzio of Chieti-Pescara, 66100 Chieti, Italy.
Vittoria CarnicelliDepartment of Pathology, University of Pisa, 56100 Pisa, Italy.
Clementina ManeraDepartment of Pharmacy, University of Pisa, 56126 Pisa, Italy.
Maurizio RonciDepartment of Medical, Oral and Biotechnological Sciences, University G. D'Annunzio of Chieti-Pescara, 66100 Chieti, Italy.ORCID 0000-0002-0797-6087
Antonio LucacchiniDepartment of Clinical and Experimental Medicine, University of Pisa, 56126 Pisa, Italy.
Riccardo ZucchiDepartment of Pathology, University of Pisa, 56100 Pisa, Italy.
Laura GiustiSchool of Pharmacy, University of Camerino, 62032 Camerino, Italy.ORCID 0000-0001-7366-1932
Grazia ChielliniDepartment of Pathology, University of Pisa, 56100 Pisa, Italy.ORCID 0000-0001-6703-5820

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neurodegenerative diseases (NDDs) are progressive multifactorial disorders of the nervous system sharing common pathogenic features, including intracellular misfolded protein aggregation, mitochondrial deficit, and inflammation. Taking into consideration the multifaceted nature of NDDs, development of multitarget-directed ligands (MTDLs) has evolved as an attractive therapeutic strategy. Compounds that target the cannabinoid receptor type II (CB2R) are rapidly emerging as novel effective MTDLs against common NDDs, such as Alzheimer's disease (AD). We recently developed the first CB2R bitopic/dualsteric ligand, namely FD22a, which revealed the ability to induce neuroprotection with fewer side effects. To explore the potential of FD22a as a multitarget drug for the treatment of NDDs, we investigated here its ability to prevent the toxic effect of β-amyloid (Aβ

Indexed as

Amyloid beta-PeptidesAutophagyBasic Helix-Loop-Helix Leucine Zipper Transcription FactorsProteomicsReceptor, Cannabinoid, CB2Cell Line, TumorHumansLigandsNeurogliaAmyloid beta-PeptidesBasic Helix-Loop-Helix Leucine Zipper Transcription FactorsLigandsReceptor, Cannabinoid, CB2TFEB protein, humanautophagycannabinoid receptor type II (CBR2)neuroinflammationproteomicTFEBβ-amyloid

Identifiers

PMID38786097
PMCPMC11119469

What Socratic 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 Socratic graph.