Evidence map›Paper›PMID 35968275›Full record

ArticleFrontiers in neurology2022

Construction and validation of a glioblastoma prognostic model based on immune-related genes.

Kate Huang, Changjun Rao, Qun Li, Jianglong Lu, Zhangzhang Zhu, Chengde Wang, Ming Tu, Chaodong Shen, Shuizhi Zheng, Xiaofang Chen and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neurology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Biomarkers of immunotherapy in glioblastoma.Neuro-oncology practice · 2024
    Review
  4. Article
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 at 2 institutions in 1 country.

Kate HuangDepartment of Pathology, First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Changjun RaoDepartment of Neurosurgery, First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Qun LiDepartment of Neurosurgery, First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Jianglong LuDepartment of Neurosurgery, First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Zhangzhang ZhuDepartment of Neurosurgery, First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Chengde WangDepartment of Neurosurgery, First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Ming TuDepartment of Neurosurgery, First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Chaodong ShenDepartment of Neurosurgery, First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Shuizhi ZhengDepartment of Neurosurgery, First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Xiaofang ChenDepartment of Neurosurgery, First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Fangfang LvDepartment of Pediatric Pulmonology, The Second Affiliated Hospital and Yuying Children's Hospital, Wenzhou Medical University, Wenzhou, China.
First Affiliated Hospital of Wenzhou Medical University · CNWenzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Glioblastoma multiforme (GBM) is a common malignant brain tumor with high mortality. It is urgently necessary to develop a new treatment because traditional approaches have plateaued. Purpose: Here, we identified an immune-related gene (IRG)-based prognostic signature to comprehensively define the prognosis of GBM. Methods: Glioblastoma samples were selected from the Chinese Glioma Genome Atlas (CGGA). We retrieved IRGs from the ImmPort data resource. Univariate Cox regression and LASSO Cox regression analyses were used to develop our predictive model. In addition, we constructed a predictive nomogram integrating the independent predictive factors to determine the one-, two-, and 3-year overall survival (OS) probabilities of individuals with GBM. Additionally, the molecular and immune characteristics and benefits of ICI therapy were analyzed in subgroups defined based on our prognostic model. Finally, the proteins encoded by the selected genes were identified with liquid chromatography-tandem mass spectrometry and western blotting (WB). Results: Six IRGs were used to construct the predictive model. The GBM patients were categorized into a high-risk group and a low-risk group. High-risk group patients had worse survival than low-risk group patients, and stronger positive associations with multiple tumor-related pathways, such as angiogenesis and hypoxia pathways, were found in the high-risk group. The high-risk group also had a low IDH1 mutation rate, high PTEN mutation rate, low 1p19q co-deletion rate and low MGMT promoter methylation rate. In addition, patients in the high-risk group showed increased immune cell infiltration, more aggressive immune activity, higher expression of immune checkpoint genes, and less benefit from immunotherapy than those in the low-risk group. Finally, the expression levels of TNC and SSTR2 were confirmed to be significantly associated with patient prognosis by protein mass spectrometry and WB. Conclusion: Herein, a robust predictive model based on IRGs was developed to predict the OS of GBM patients and to aid future clinical research.

Indexed as

glioblastomaimmune-related genesmass spectrometrynomogramprognostic modelTNC

Identifiers

PMID35968275
PMCPMC9366078
OpenAlexW4288436494

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.