Evidence map›Paper›PMID 33912195›Full record

ReviewFrontiers in immunology2021

Targeting the Notch Signaling Pathway in Chronic Inflammatory Diseases.

Panagiotis F Christopoulos, Torleif T Gjølberg, Stig Krüger, Guttorm Haraldsen, Jan Terje Andersen, Eirik Sundlisæter

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed, 3 pooled it
12.3field-weighted citation impact, top 1% 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

61 citing papers in PubMed, 3 syntheses or guidelines pooled it, 110 citations in OpenAlex.

  1. Pooled it
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  14. Notch2-expressing CD4Cellular & molecular immunology · 2025
    Article
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1 more citing papers are in PubMed but not listed here.

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

6 authors at 2 institutions in 1 country.

Panagiotis F ChristopoulosDepartment of Pathology, University of Oslo and Oslo University Hospital, Oslo, Norway.
Torleif T GjølbergInstitute of Clinical Medicine and Department of Pharmacology, University of Oslo and Oslo University Hospital, Oslo, Norway.
Stig KrügerDepartment of Pathology, University of Oslo and Oslo University Hospital, Oslo, Norway.
Guttorm HaraldsenDepartment of Pathology, University of Oslo and Oslo University Hospital, Oslo, Norway.
Jan Terje AndersenInstitute of Clinical Medicine and Department of Pharmacology, University of Oslo and Oslo University Hospital, Oslo, Norway.
Eirik SundlisæterDepartment of Pathology, University of Oslo and Oslo University Hospital, Oslo, Norway.
University of Oslo · NOOslo University Hospital · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Notch signaling pathway regulates developmental cell-fate decisions and has recently also been linked to inflammatory diseases. Although therapies targeting Notch signaling in inflammation in theory are attractive, their design and implementation have proven difficult, at least partly due to the broad involvement of Notch signaling in regenerative and homeostatic processes. In this review, we summarize the supporting role of Notch signaling in various inflammation-driven diseases, and highlight efforts to intervene with this pathway by targeting Notch ligands and/or receptors with distinct therapeutic strategies, including antibody designs. We discuss this in light of lessons learned from Notch targeting in cancer treatment. Finally, we elaborate on the impact of individual Notch members in inflammation, which may lay the foundation for development of therapeutic strategies in chronic inflammatory diseases.

Indexed as

AntibodiesAnti-Inflammatory AgentsAutoimmune DiseasesAutoimmunityChronic DiseaseHumansInflammationMolecular Targeted TherapyReceptors, NotchSignal TransductionAntibodiesAnti-Inflammatory AgentsReceptors, Notchautoimmunitybiological therapeuticsgamma-secretase inhibitors (GSIs)inflammationneutralizing antibodiesnotch

Identifiers

PMID33912195
PMCPMC8071949
OpenAlexW3153313562

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.