Evidence map›Paper›PMID 40155506›Full record

ArticleScientific reports2025

Bioinformatics analysis to identify key invasion related genes and construct a prognostic model for glioblastoma.

Jintao Tian, Jinxi Zhao, Zhixing Xu, Bohu Liu, Jun Pu, Hongwen Li, Qingchun Lei, Yu Zhao, Weilin Zhou, Xuhui Li and 1 more

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

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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

1 citing paper in PubMed.

  1. 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

11 authors.

Jintao Tian *Department of Neurosurgery, The Second Affiliated Hospital of Kunming Medical University, Kunming, 650101, China.
Jinxi Zhao *Department of Neurosurgery, The Second Affiliated Hospital of Kunming Medical University, Kunming, 650101, China.
Zhixing XuDepartment of Neurosurgery, The Pu'er People's Hospital, Puer, 665000, China.
Bohu LiuDepartment of Neurosurgery, The Kunming First People's Hospital, Kunming, 650011, China.
Jun PuDepartment of Neurosurgery, The Second Affiliated Hospital of Kunming Medical University, Kunming, 650101, China.
Hongwen LiDepartment of Neurosurgery, The Dali People's Hospital, Dali, 671000, China.
Qingchun LeiDepartment of Neurosurgery, The Pu'er People's Hospital, Puer, 665000, China.
Yu ZhaoDepartment of Neurosurgery, The Second Affiliated Hospital of Kunming Medical University, Kunming, 650101, China.
Weilin ZhouDepartment of Neurosurgery, The Second Affiliated Hospital of Kunming Medical University, Kunming, 650101, China.
Xuhui LiDepartment of Neurosurgery, The Second Affiliated Hospital of Kunming Medical University, Kunming, 650101, China. 529316932@qq.com.
Xiaobin HuangDepartment of Neurosurgery, The Second Affiliated Hospital of Kunming Medical University, Kunming, 650101, China. hxbynyx@163.com.

Funding

National Clinical Medical Research Center for Neurological diseases GF2020001National Natural Science Foundation of China 82160512
6 · The paper itself

Abstract

Glioblastoma (GBM) is the most common and lethal brain tumor with limited therapeutic strategies and incomplete studies on its progression and mechanisms. This study aims to reveal potential prognostic marker genes associated with GBM cell invasion, and establish an effective prognostic model for GBM patients. Differentially expressed genes (DEGs) were screened from The Cancer Genome Atlas (TCGA) and the Chinese Glioma Genome Atlas (CGGA), differentially invasive-related genes was obtained, qRT-PCR was used to verify gene expression. The risk scores of individual patients, univariate and multivariate Cox regression were analyzed to investigate the correlation between risk values and glioblastoma, Finally, the risk scores with the prognostic clinical characteristics of the patients, such as PFS, OS were used to build a comprehensive GBM prognostic model. Five DEGs (GZMB, COL22A1, MSTN, CRYGN and OSMR) were significantly associated with GBM prognosis. Pseudotemporal analysis, risk scores (PFS, OS) based on tumor cells revealed that prognostic genes were associated with tumor proliferation and progression. The final prognostic model was developed and validated with good performance with higher accuracy(C-index: 0.675), and it was found that the risk value can serve as an independent prognostic factor for patients with glioblastoma (p < 0.05). We constructed a comprehensive prognostic model related to invasion in GBM patients using genetic profiles, survival curves, immune infiltration, and radiotherapy face susceptibility. The model has good predictive ability.

Indexed as

Biomarkers, TumorBrain NeoplasmsComputational BiologyGlioblastomaFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHumansMaleMiddle AgedNeoplasm InvasivenessPrognosisBiomarkers, TumorGlioblastomaImmunotherapyInvasion-related genePrognostic model

Identifiers

PMID40155506
PMCPMC11953321

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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.