Evidence map›Paper›PMID 36071287›Full record

ArticleMedical oncology (Northwood, London, England)2022

Exploring the inverse association of glioblastoma multiforme and Alzheimer's disease via bioinformatics analysis.

Jiayang Cai, Liguo Ye, Yuanyuan Hu, Zhang Ye, Lun Gao, Yixuan Wang, Qian Sun, Shiao Tong, Ji'an Yang, Qianxue Chen

Abstract read
PubMed Publisher
In one paragraph

Article in Medical oncology (Northwood, London, England), 2022. 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
1.2field-weighted citation impact, top 22% 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, 11 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Pericytes Are Immunoregulatory Cells in Glioma Genesis and Progression.International journal of molecular sciences · 2024
    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

10 authors at 2 institutions in 1 country.

Jiayang Cai *Department of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, 430060, Hubei, China.
Liguo Ye *Department of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, 430060, Hubei, China.
Yuanyuan HuDepartment of Ophthalmology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.
Zhang YeDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, 430060, Hubei, China.
Lun GaoDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, 430060, Hubei, China.
Yixuan WangDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, 430060, Hubei, China.
Qian SunDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, 430060, Hubei, China.
Shiao TongDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, 430060, Hubei, China.
Ji'an YangDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, 430060, Hubei, China. jayang@whu.edu.cn.
Qianxue ChenDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, 430060, Hubei, China. chenqx666@whu.edu.cn.ORCID http://orcid.org/0000-0002-5287-8240
Wuhan University · CNTongji Hospital · CN

Funding

Innovative Research Group Project of the National Natural Science Foundation of China 82072764Natural Science Foundation of Hubei Province 2020CFB256
6 · The paper itself

Abstract

Glioblastoma multiforme (GBM) and Alzheimer's disease (AD) are two major diseases in the nervous system with a similar peak age of onset, which has the typical characteristics of high cost, difficult treatment, and poor prognosis. Epidemiological studies and a few molecular biological studies have hinted at an opposite relationship between AD and GBM. However, there are few studies on their reverse relationship, and the regulatory mechanism is still unclear, indicating that further systematic research is urgently needed. Our study firstly employs advanced bioinformatics methods to explore the inverse relationship between them and find various target drugs. We obtained the gene expression dataset from public databases (GEO, TCGA, and GTEx). Then, we identified 122 differentially expressed genes (DEGs) of AD and GBM. Four significant gene modules were identified through protein-protein interaction (PPI) and module construction, and 13 hub genes were found using cytoHubba. We constructed co-expression networks and found various target drugs through these hub genes. Functional enrichment analysis revealed that the AMPK pathway, cell cycle, and cellular senescence play important roles in AD and GBM. Our study may provide a potential direction for studying the opposite molecular mechanism of AD and GBM in the future.

Indexed as

Alzheimer DiseaseGlioblastomaComputational BiologyGene Expression ProfilingGene Expression Regulation, NeoplasticHumansAlzheimer’s diseaseBioinformaticsGlioblastoma multiformeHub genes

Identifiers

PMID36071287
OpenAlexW4294884496

What Socratic holds

Textmetadata
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 Socratic graph.