Evidence map›Paper›PMID 39040060›Full record

ArticleiScience2024

The role of m6A modification in the risk prediction and Notch1 pathway of Alzheimer's disease.

Yingdan Qiao, Yingna Mei, Minqi Xia, Deng Luo, Ling Gao

Abstract read
In one paragraph

Article in iScience, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. The Role of the Notch1 Signaling Pathway in the Pathogenesis and Treatment of Diabetic Foot: A Review.Diabetes therapy : research, treatment and education of diabetes and related disorders · 2026
    Review
  2. Article
  3. mNature reviews. Neuroscience · 2026
    Review
  4. Article
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  6. Article
  7. Article
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  9. The mCells · 2025
    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

5 authors.

Yingdan QiaoDepartment of Endocrinology & Metabolism, Renmin Hospital of Wuhan University, Wuhan, P.R. China.
Yingna MeiDepartment of Endocrinology & Metabolism, Renmin Hospital of Wuhan University, Wuhan, P.R. China.
Minqi XiaDepartment of Endocrinology & Metabolism, Renmin Hospital of Wuhan University, Wuhan, P.R. China.
Deng LuoDepartment of Endocrinology & Metabolism, Renmin Hospital of Wuhan University, Wuhan, P.R. China.
Ling GaoDepartment of Endocrinology & Metabolism, Renmin Hospital of Wuhan University, Wuhan, P.R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

N6-methyladenosine (m6A) methylation and abnormal immune responses are implicated in neurodegenerative diseases, yet their relationship in Alzheimer's disease (AD) remains unclear. We obtained AD datasets from GEO databases and used AD mouse and cell models, observing abnormal expression of m6A genes in the AD group, alongside disruptions in the immune microenvironment. Key m6A genes (YTHDF2, LRPPRC, and FTO) selected by machine learning were associated with the Notch pathway, with FTO and Notch1 displaying the strongest correlation. Specifically, FTO expression decreased and m6A methylation of Notch1 increased in AD mouse and cell models. We further silenced FTO expression in HT22 cells, resulting in upregulation of the Notch1 signaling pathway. Additionally, increased Notch1 expression in dendritic cells heightened inflammatory cytokine secretion

Indexed as

Biological sciencesMolecular neuroscienceNeuroscience

Identifiers

PMID39040060
PMCPMC11261416

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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.