Evidence map›Paper›PMID 39409132›Full record

ReviewInternational journal of molecular sciences2024

The Complex Interplay of TGF-β and Notch Signaling in the Pathogenesis of Fibrosis.

Nadezhda Bakalenko, Evdokiya Kuznetsova, Anna Malashicheva

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing 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

27 citing papers in PubMed.

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  13. Biliary atresia-related liver fibrosis.Frontiers in cell and developmental biology · 2026
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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

3 authors.

Nadezhda BakalenkoInstitute of Cytology, Russian Academy of Sciences, St-Petersburg 194064, Russia.ORCID 0000-0002-1134-1711
Evdokiya KuznetsovaInstitute of Cytology, Russian Academy of Sciences, St-Petersburg 194064, Russia.
Anna MalashichevaInstitute of Cytology, Russian Academy of Sciences, St-Petersburg 194064, Russia.ORCID 0000-0002-0820-2913

Funding

Ministry of Science and Higher Education of the Russian Federation No. 075-15-2021-1075 dated 09/28/2021
6 · The paper itself

Abstract

Fibrosis is a major medical challenge, as it leads to irreversible tissue remodeling and organ dysfunction. Its progression contributes significantly to morbidity and mortality worldwide, with limited therapeutic options available. Extensive research on the molecular mechanisms of fibrosis has revealed numerous factors and signaling pathways involved. However, the interactions between these pathways remain unclear. A comprehensive understanding of the entire signaling network that drives fibrosis is still missing. The TGF-β and Notch signaling pathways play a key role in fibrogenesis, and this review focuses on their functional interplay and molecular mechanisms. Studies have shown synergy between TGF-β and Notch cascades in fibrosis, but antagonistic interactions can also occur, especially in cardiac fibrosis. The molecular mechanisms of these interactions vary depending on the cell context. Understanding these complex and context-dependent interactions is crucial for developing effective strategies for treating fibrosis.

Indexed as

FibrosisReceptors, NotchSignal TransductionTransforming Growth Factor betaAnimalsHumansReceptors, NotchTransforming Growth Factor betafibrosisNICDNotch signalingsignaling crosstalkSMADTGF-β pathway

Identifiers

PMID39409132
PMCPMC11477142

What OpenQuestion holds

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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.