Evidence map›Paper›PMID 37759516›Full record

ArticleCells2023

Anti-Inflammatory Effects of Synthetic Peptides Based on Glucocorticoid-Induced Leucine Zipper (GILZ) Protein for the Treatment of Inflammatory Bowel Diseases (IBDs).

Musetta Paglialunga, Sara Flamini, Raffaele Contini, Marta Febo, Erika Ricci, Simona Ronchetti, Oxana Bereshchenko, Graziella Migliorati, Carlo Riccardi, Stefano Bruscoli

Open access · goldAbstract read
In one paragraph

Article in Cells, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
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  3. Review
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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 1 institution in 1 country.

Musetta PaglialungaDepartment of Medicine and Surgery, Section of Pharmacology, University of Perugia, 06132 Perugia, Italy.ORCID 0000-0002-9133-8095
Sara FlaminiDepartment of Medicine and Surgery, Section of Pharmacology, University of Perugia, 06132 Perugia, Italy.
Raffaele ContiniDepartment of Medicine and Surgery, Section of Pharmacology, University of Perugia, 06132 Perugia, Italy.
Marta FeboDepartment of Medicine and Surgery, Section of Pharmacology, University of Perugia, 06132 Perugia, Italy.
Erika RicciDepartment of Medicine and Surgery, Section of Pharmacology, University of Perugia, 06132 Perugia, Italy.
Simona RonchettiDepartment of Medicine and Surgery, Section of Pharmacology, University of Perugia, 06132 Perugia, Italy.ORCID 0000-0002-5639-4243
Oxana BereshchenkoDepartment of Philosophy, Social Sciences and Education, University of Perugia, 06123 Perugia, Italy.
Graziella MiglioratiDepartment of Medicine and Surgery, Section of Pharmacology, University of Perugia, 06132 Perugia, Italy.ORCID 0000-0002-9475-6399
Carlo RiccardiDepartment of Medicine and Surgery, Section of Pharmacology, University of Perugia, 06132 Perugia, Italy.
Stefano BruscoliDepartment of Medicine and Surgery, Section of Pharmacology, University of Perugia, 06132 Perugia, Italy.ORCID 0000-0003-0313-1615
University of Perugia · IT

Funding

CCF 504854
6 · The paper itself

Abstract

Glucocorticoids (GCs) are commonly used to treat autoimmune and inflammatory diseases, but their clinical effects and long-term use can lead to serious side effects. New drugs that can replace GCs are needed. Glucocorticoid-induced leucine zipper (GILZ) is induced by GCs and mediates many of their anti-inflammatory effects, such as inhibiting the pro-inflammatory molecule NF-κB. The GILZ C-terminal domain (PER region) is responsible for GILZ/p65NF-κB interaction and consequent inhibition of its transcriptional activity. A set of five short peptides spanning different parts of the PER region of GILZ protein was designed, and their anti-inflammatory activity was tested, both in vitro and in vivo. We tested the biological activity of GILZ peptides in human lymphocytic and monocytic cell lines to evaluate their inhibitory effect on the NF-κB-dependent expression of pro-inflammatory cytokines. Among the tested peptides, the peptide named PEP-1 demonstrated the highest efficacy in inhibiting cell activation in vitro. Subsequently, PEP-1 was further evaluated in two in vivo experimental colitis models (chemically induced by DNBS administration and spontaneous colitis induced in IL-10 knock-out (KO) mice (to assess its effectiveness in counteracting inflammation. Results show that PEP-1 reduced disease severity in both colitis models associated with reduced NF-κB pro-inflammatory activity in colon lamina propria lymphocytes. This study explored GILZ-based 'small peptides' potential efficacy in decreasing lymphocyte activation and inflammation associated with experimental inflammatory bowel diseases (IBDs). Small peptides have several advantages over the entire protein, including higher selectivity, better stability, and bioavailability profile, and are easy to synthesize and cost-effective. Thus, identifying active GILZ peptides could represent a new class of drugs for treating IBD patients.

Indexed as

Anti-Inflammatory AgentsInflammatory Bowel DiseasesPeptidesTranscription FactorsAnimalsColitisCytokinesDisease Models, AnimalHumansLeucine ZippersMaleMiceMice, Inbred C57BLNF-kappa BAnti-Inflammatory AgentsCytokinesDsip1 protein, mouseNF-kappa BPeptidesTranscription FactorsTSC22D3 protein, humanGILZglucocorticoidsIBDsinflammationNF-κB

Identifiers

PMID37759516
PMCPMC10528232
OpenAlexW4386814775

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.