Evidence map›Paper›PMID 37920383›Full record

ArticleFrontiers in aging neuroscience2023

Systematic analysis of cuproptosis-related genes in immunological characterization and predictive drugs in Alzheimer's disease.

Bin Nie, Yefen Duan, Xuelong Xie, Lihua Qiu, Shaorui Shi, Zhili Fan, Xuxiang Zheng, Ling Jiang

Open access · goldAbstract read
In one paragraph

Article in Frontiers in aging neuroscience, 2023. 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
0.9field-weighted citation impact, top 26% 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

7 citing papers in PubMed, 5 citations in OpenAlex.

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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

8 authors at 1 institution in 1 country.

Bin NieDepartment of Clinical Laboratory, The Second People's Hospital of Yibin·West China Yibin Hospital, Sichuan University, Yibin, China.
Yefen DuanDepartment of Clinical Laboratory, Yibin No. 4 People's Hospital, Yibin, China.
Xuelong XieDepartment of Clinical Laboratory, The Second People's Hospital of Yibin·West China Yibin Hospital, Sichuan University, Yibin, China.
Lihua QiuImaging Department, The Second People's Hospital of Yibin·West China Yibin Hospital, Sichuan University, Yibin, China.
Shaorui ShiDepartment of Clinical Laboratory, The Second People's Hospital of Yibin·West China Yibin Hospital, Sichuan University, Yibin, China.
Zhili FanDepartment of Clinical Laboratory, The Second People's Hospital of Yibin·West China Yibin Hospital, Sichuan University, Yibin, China.
Xuxiang ZhengDepartment of Clinical Laboratory, The Second People's Hospital of Yibin·West China Yibin Hospital, Sichuan University, Yibin, China.
Ling JiangDepartment of Neurology, The Second People's Hospital of Yibin·West China Yibin Hospital, Sichuan University, Yibin, China.
Second People’s Hospital of Yibin · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: This study aimed to make a systematic analysis of cuproptosis-related genes (CRGs) in immunological characterization and predictive drugs in Alzheimer's disease (AD) through bioinformatics and biological experiments. Methods: The molecular clusters related to CRGs and associated immune cell infiltrations in AD were investigated. The diagnostic models were constructed for AD and different AD subtypes. Moreover, drug prediction and molecular docking were also performed. Subsequently, a molecular dynamics (MD) simulation was conducted to further verify the findings. Finally, RT-qPCR validation was performed. Results: The characterization of 12 AD-related CRGs was evaluated in AD, and a diagnostic model for AD showed a satisfying discrimination power based on five CRGs by LASSO regression analysis. The dysregulated CRGs and activated immune responses partially differed between patients with AD and healthy subjects. Furthermore, two molecular subtypes (clusters A and B) with different immune infiltration characteristics in AD were identified. Similarly, a diagnostic model for different AD subtypes was built with nine CRGs, which achieved a good performance. Molecular docking revealed the optimum conformation of CHEMBL261454 and its target gene CSNK1D, which was further validated by MD simulation. The RT-qPCR results were consistent with those of the comprehensive analysis. Conclusion: This study systematically elucidated the complex relationship between cuproptosis and AD, providing novel molecular targets for treatment and diagnosis biomarkers of AD.

Indexed as

Alzheimer’s diseasecuproptosisdiagnostic modelimmune microenvironmentmolecular docking

Identifiers

PMID37920383
PMCPMC10618683
OpenAlexW4387741665

What OpenQuestion holds

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LicenceCC BY
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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.