Evidence map›Paper›PMID 41255833›Full record

ArticleIranian journal of biotechnology2025

Single-Cell RNA-Seq Dissects Specific Marker in Glioblastoma Based on Gene Regulatory Networks.

Shenglan Li, Yanjie Lan, Jiachen Wang, Zhuang Kang, Mengqian Huang, Rong Zhang, Wenbin Li

Abstract read
In one paragraph

Article in Iranian journal of biotechnology, 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

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

1 citing paper in PubMed.

  1. 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

7 authors.

Shenglan LiDepartment of Neuro-oncology, Cancer Center, Beijing Tiantan Hospital, Capital Medical University, Beijing, 100071, China.
Yanjie LanDepartment of Neuro-oncology, Cancer Center, Beijing Tiantan Hospital, Capital Medical University, Beijing, 100071, China.
Jiachen WangDepartment of Neuro-oncology, Cancer Center, Beijing Tiantan Hospital, Capital Medical University, Beijing, 100071, China.
Zhuang KangDepartment of Neuro-oncology, Cancer Center, Beijing Tiantan Hospital, Capital Medical University, Beijing, 100071, China.
Mengqian HuangDepartment of Neuro-oncology, Cancer Center, Beijing Tiantan Hospital, Capital Medical University, Beijing, 100071, China.
Rong ZhangDepartment of Neuro-oncology, Cancer Center, Beijing Tiantan Hospital, Capital Medical University, Beijing, 100071, China.
Wenbin LiDepartment of Neuro-oncology, Cancer Center, Beijing Tiantan Hospital, Capital Medical University, Beijing, 100071, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Glioblastoma (GBM) is one of the most aggressive and common tumors of the central nervous system (CNS), distinguished by its significant intratumoral heterogeneity and poor prognosis, with a median overall survival of approximately 15 months. Recent advances in single-cell RNA sequencing (scRNA-seq) have provided deeper insights into the molecular subtypes and heterogeneity of GBM, which include the proneural (PN), classical (CL), and mesenchymal (MES) subtypes. Objectives: This study hypothesizes that constructing gene regulatory networks (GRNs) using single-cell RNA sequencing (scRNA-seq) data can elucidate the complex regulatory mechanisms underlying glioblastoma (GBM) heterogeneity. The primary aim is to identify key regulators and subtype-specific markers in GBM through the integration of scRNA-seq and GRNs, with the ultimate goal of discovering novel prognostic biomarkers that can improve patient stratification and treatment outcomes. Materials and Methods: Malignant cells were identified based on inferred copy number variations (CNVs) from scRNA-seq data. Consensus clustering of expression profiles was used to assign GBM subtypes. Analyses of differential gene expression, ligand-receptor interactions, pathway activities, and responses to immune checkpoint inhibitors were conducted. GRNs were constructed by retaining co-expressed transcription factor (TF)-gene pairs with enriched transcription-binding motifs. Bulk RNA-seq data were then used to validate marker expression and assess prognostic value. Results: Distinct functional roles and molecular characteristics were observed across GBM subtypes. Subtype-specific GRNs revealed both unique and shared regulatory features. GATA binding protein 3 (GATA3) emerged as a potential prognostic marker, showing correlation with homologous recombination deficiency (HRD) and patient outcomes. Conclusions: Subtype-resolved GRN analysis of GBM provides valuable insights into intratumoral heterogeneity and regulatory mechanisms. GATA3 may serve as a novel biomarker for prognosis and therapeutic stratification in GBM patients.

Indexed as

CNVs InferenceGene Regulatory NetworkGlioblastomaHeterogeneitySingle Cell Subtype

Identifiers

PMID41255833
PMCPMC12620859

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