Khatun Mst Sahida, Rashid Mohammad Mamun Ur, Ullah Ahsan, Kim Hyung-Ryong
Department of Pharmacology, College of Dentistry, Jeonbuk National University, Jeonju, Republic of Korea.
Department of Pharmacology, Institute of New Drug Development, Jeonbuk National University Medical School, Jeonju, Republic of Korea.
Sci Rep. 2025 Jul 1;15(1):21422. doi: 10.1038/s41598-025-06799-9.
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.
TMBIM6是一种位于内质网的含跨膜BAX抑制基序6的蛋白,与多种细胞过程和癌症进展相关。先前的研究表明,TMBIM6与多种癌症类型患者的生存率之间存在显著关联。然而,由于缺乏针对TMBIM6与胶质瘤之间相关性的广泛研究,因此有必要进行全面调查,以探索其作为胶质瘤预后标志物的潜力。本研究通过使用来自TCGA(癌症基因组图谱)、GEO(基因表达综合数据库)和CGGA(中国胶质瘤基因组图谱)数据库的数据,以及组织微阵列玻片的组织病理学分析,研究了TMBIM6的预后价值。生存分析证实了TMBIM6在胶质瘤中的预后意义,共表达分析确定了与TMBIM6正相关和负相关的基因,富集分析表明TMBIM6与内质网中的蛋白质加工和NOD样受体信号通路有关。观察到TMBIM6表达与免疫浸润之间存在强烈相关性,尤其是与M2巨噬细胞。此外,hsa-miR-128-3p被确定为TMBIM6的上游调节因子。这些发现突出了TMBIM6作为胶质瘤预后生物标志物的潜力,为其在胶质瘤进展中的作用提供了新的见解。