Evidence map›Paper›PMID 41013661›Full record

ReviewMolecular neurodegeneration2025

The Hippo signaling pathway as a therapeutic target in Alzheimer's disease.

Doris Chen, Stella Wigglesworth-Littlewood, Frank J Gunn-Moore

Abstract readReview
In one paragraph

Review in Molecular neurodegeneration, 2025. 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
  6. Article
  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

3 authors.

Doris ChenSchool of Biology, University of St Andrews, St Andrews, KY16 9TF, UK.ORCID 0009-0004-8649-6736
Stella Wigglesworth-LittlewoodSchool of Biology, University of St Andrews, St Andrews, KY16 9TF, UK.ORCID 0000-0002-7610-9462
Frank J Gunn-MooreSchool of Biology, University of St Andrews, St Andrews, KY16 9TF, UK. fjg1@st-andrews.ac.uk.ORCID 0000-0003-3422-3387

Funding

Alzheimer's Research UK Alzheimer's Research UKUniversity of St Andrews University of St Andrews
6 · The paper itself

Abstract

The Hippo signaling pathway is well-known for its regulation of organ size, cell proliferation, apoptosis, and cell migration and differentiation. Recent studies have demonstrated that Hippo signaling also plays important roles in the nervous system, being involved in neuroinflammation, neuronal differentiation, and neuronal death and degeneration. As such, dysregulation of Hippo signaling, particularly of its core kinases MST1/2 and LATS1/2, has begun to attract attention in the Alzheimer's disease (AD) field. Here, we discuss the therapeutic potential of targeting the Hippo pathway in AD by providing an overview of Hippo signaling with regards to its function in the nervous system, evidence for its dysregulation in AD patients and models, and recent studies involving genetic or pharmacological modulation of this pathway in AD.

Indexed as

Alzheimer DiseaseProtein Serine-Threonine KinasesSignal TransductionAnimalsHippo Signaling PathwayHumansProtein Serine-Threonine KinasesAlzheimer’s diseaseHippo signalingNeuronal death

Identifiers

PMID41013661
PMCPMC12465945

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.