Evidence map›Paper›PMID 40394049›Full record

ArticleScientific reports2025

TMBIM1 promotes epithelial mesenchymal transition by accelerating autophagic degradation of E-cadherin in glioblastoma.

Lun Gao, Junhui Liu, Yong Li, Ji'an Yang, Jiayang Cai, Long Wang, Zhang Ye, Shi'ao Tong, Gang Deng, Qianxue Chen 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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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.

Lun Gao *Department of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, 430060, China.
Junhui Liu *Department of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, 430060, China.
Yong LiDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, 430060, China.
Ji'an YangDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, 430060, China.
Jiayang CaiDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, 430060, China.
Long WangDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, 430060, China.
Zhang YeDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, 430060, China.
Shi'ao TongDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, 430060, China.
Gang DengDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, 430060, China. gang.deng@whu.edu.cn.
Qianxue ChenDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, 430060, China. chenqx666@whu.edu.cn.
Qiang CaiDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, 430060, China. caiqno@whu.edu.cn.

Funding

Fundamental Research Funds for the Central Universities 2042021kf0090National Natural Science Foundation of China 81671306National Natural Science Foundation of China 81971158National Natural Science Foundation of China 82001311National Natural Science Foundation of China 82072764Wuhan Science and Technology Plan Project 2019020701011470
6 · The paper itself

Abstract

Glioblastoma (GBM; WHO grade IV) is well known for its highly aggressive and recurrent nature and accounts for approximately 50% of all gliomas. Dysregulation of epithelial-mesenchymal transition (EMT) can lead to malignant progression of GBM. Therefore, it is an urgent need to delineate the mechanisms by which molecular drivers affect EMT in GBM. We found for the first time that transmembrane BAX inhibitor motif-containing 1 (TMBIM1) was overexpressed in GBM tissues compared with nontumor brain tissues and that its expression level was correlated with the degree of malignancy of glioma. Patients with high TMBIM1 expression had shorter overall survival times than those with low TMBIM1 expression. Importantly, TMBIM1 induced EMT and autophagy, and inhibition of autophagy reversed TMBIM1-induced EMT in both in vitro and in vivo assays. TMBIM1 induced EMT by downregulating E-cadherin expression, which mediated by in-habitation of autophagic degradation of E-cadherin. Inhibition of TMBIM1 expression dramatically decreased the levels of p-AMPKα Thr172 and p-ULK1 Ser317 in U87 and U251 cells and increased the level of p-mTOR Ser2448. In addition, inhibition of AMPK (adenosine monophosphate-activated protein kinase)/mTOR (mammalian target of rapamycin)/ULK1 (unc-51-like autophagy-activating kinase 1) axis partially attenuated TMBIM1-induced autophagy. Our study provides a novel mechanism for the regulation of EMT in the process of GBM invasion and migration, indicating that suppression of TMBIM1 activity to attenuate autophagy may be a potential strategy for the treatment of GBM.

Indexed as

Antigens, CDAutophagyBrain NeoplasmsCadherinsEpithelial-Mesenchymal TransitionGlioblastomaMembrane ProteinsAnimalsAutophagy-Related Protein-1 HomologCell Line, TumorFemaleGene Expression Regulation, NeoplasticHumansIntracellular Signaling Peptides and ProteinsMaleMiceAntigens, CDAutophagy-Related Protein-1 HomologCadherinsCDH1 protein, humanIntracellular Signaling Peptides and ProteinsMembrane ProteinsTOR Serine-Threonine KinasesULK1 protein, humanAMPK-mTOR-ULK1 axisAutophagyEpithelial-mesenchymal transitionGlioblastomaTMBIM1

Identifiers

PMID40394049
PMCPMC12092792

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.