Evidence map›Paper›PMID 40595030›Full record

ArticleScientific reports2025

TMBIM6 promotes glioma progression according to integrated bioinformatics and experimental evidence.

Mst Sahida Khatun, Mohammad Mamun Ur Rashid, Ahsan Ullah, Hyung-Ryong Kim

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. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

4 authors.

Mst Sahida Khatun *Department of Pharmacology, College of Dentistry, Jeonbuk National University, Jeonju, Republic of Korea.
Mohammad Mamun Ur Rashid *Department of Pharmacology, Institute of New Drug Development, Jeonbuk National University Medical School, Jeonju, Republic of Korea.
Ahsan UllahSchool of Pharmacy and Institute of New Drug Development, Jeonbuk National University, Jeonju, Republic of Korea.
Hyung-Ryong KimDepartment of Pharmacology, College of Dentistry, Jeonbuk National University, Jeonju, Republic of Korea. hrkimdp@gmail.com.

Funding

National Research Foundation of Korea 2023R1A2C2003446
6 · The paper itself

Abstract

TMBIM6, a transmembrane BAX inhibitor motif containing 6, located in the endoplasmic reticulum, is linked to various cellular processes and cancer progression. Previous investigations showed a substantial association between TMBIM6 and survival in patients diagnosed with various cancer types. However, the lack of extensive studies addressing the correlation between TMBIM6 and gliomas necessitates a comprehensive investigation to explore its potential as a prognosis marker for glioma. This study investigates TMBIM6's prognostic value by using data from TCGA (The Cancer Genome Atlas), GEO (Gene Expression Omnibus), and CGGA (Chinese Glioma Genome Atlas) databases, along with histopathological analysis of tissue microarray slide. Survival analysis confirmed the prognostic significance of TMBIM6 in glioma, while co-expression analysis identified positively and negatively correlated genes with TMBIM6, and Enrichment analysis suggested TMBIM6's association with protein processing in the ER and NOD-like receptor signaling pathways. A strong correlation was observed between TMBIM6 expression and immune infiltration, especially with M2 macrophages. Additionally, hsa-miR-128-3p was identified as an upstream regulator of TMBIM6. These findings highlight TMBIM6's potential as a prognostic biomarker for glioma, offering new insights into its role in glioma progression.

Indexed as

Apoptosis Regulatory ProteinsBrain NeoplasmsComputational BiologyGliomaMembrane ProteinsBiomarkers, TumorDisease ProgressionFemaleGene Expression Regulation, NeoplasticHumansMaleMicroRNAsPrognosisSignal TransductionApoptosis Regulatory ProteinsBiomarkers, TumorMembrane ProteinsMicroRNAsBax inhibitor-1BI-1BiomarkerGBMGliomaLGGTMBIM6

Identifiers

PMID40595030
PMCPMC12219401

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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.