Evidence map›Paper›PMID 40263417›Full record

ArticleScientific reports2025

Periostin-mediated activation of NF-κB signaling promotes tumor progression and chemoresistance in glioblastoma.

Yu Shang, Yuxia Liang, Beichen Zhang, Wei Wu, Yihao Peng, Jin Wang, Ming Zhang, Chen Niu

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 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Therapeutic Potential ofInternational journal of general medicine · 2026
    Article
  6. 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

8 authors.

Yu Shang *PET-CT Center, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, 710061, Shaanxi, China.
Yuxia Liang *Department of Physical Examination, The First Hospital Affiliated to Xi'an Jiao Tong University, Xi'an, 710061, Shaanxi, China.
Beichen ZhangDepartment of Neurosurgery, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, 710061, Shaanxi, China.
Wei WuDepartment of Neurosurgery, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, 710061, Shaanxi, China.
Yihao PengFuture Technology Institute, Xi'an Jiaotong University, Xi'an, 710049, Shaanxi, China.
Jin WangFuture Technology Institute, Xi'an Jiaotong University, Xi'an, 710049, Shaanxi, China.
Ming ZhangDepartment of Radiology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, 710061, Shaanxi, China. zhangming01@xjtu.edu.cn.
Chen NiuPET-CT Center, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, 710061, Shaanxi, China. niuchen1984@163.com.

Funding

the Clinical Research Program of the First Affiliated Hospital of Xi'an Jiaotong University of China XJTU1AF-CRF-2018-006the National Natural Science Foundation of China 82102014the Shaanxi Provincial Key Industrial Innovation Chain Project 2024SF-ZDCYL-02-10
6 · The paper itself

Abstract

Glioblastoma (GBM) is the most aggressive form of diffuse glioma, characterized by high lethality. Temozolomide (TMZ)-based chemotherapy is a standard treatment for GBM, but development of chemoresistance poses a significant therapeutic challenge. Despite advances in understanding GBM biology, the mechanisms driving TMZ resistance remain unclear. Identifying vital molecular players involved in this resistance is crucial for developing new therapies. Our results indicated that periostin (POSTN) was significantly upregulated in GBM cell lines and patient samples, correlating with poorer clinical outcomes. POSTN overexpression enhanced GBM cell proliferation, migration, invasion, and chemoresistance, while lentiviral suppression of POSTN significantly reduced these behaviors. In vivo, bioluminescence imaging further confirmed the enhanced tumor growth associated with POSTN overexpression. Bioinformatics analysis was performed to explore the underlying molecular mechanism. The results revealed a strong correlation between POSTN and epithelial-mesenchymal transition (EMT) process and the tumor necrosis factor α (TNFα)-NF-κB signaling pathway. Moreover, exogenous POSTN silencing reduced IκB-kinase α (IKKα) phosphorylation, thereby decreasing NF-κB expression by limiting IκBα degradation. Collectively, our study demonstrated that POSTN-induced activation of NF-κB signaling and EMT processes promoted the malignancy and chemoresistance of GBM, suggesting that POSTN may serve as a reliable prognostic biomarker and potential therapeutic target for GBM.

Indexed as

Brain NeoplasmsCell Adhesion MoleculesDrug Resistance, NeoplasmGlioblastomaNF-kappa BSignal TransductionAnimalsCell Line, TumorCell MovementCell ProliferationDisease ProgressionEpithelial-Mesenchymal TransitionGene Expression Regulation, NeoplasticHumansMicePeriostinCell Adhesion MoleculesNF-kappa BPeriostinPOSTN protein, humanTemozolomideEMT-related phenotypesGlioblastomaNF-κB signalingPOSTNTMZ resistance

Identifiers

PMID40263417
PMCPMC12015317

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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.