TMCO1 expression promotes cell proliferation and induces epithelial-mesenchymal transformation in human gliomas.
Lun GaoZhang YeJun-Hui LiuJi-An YangYong LiJia-Yang CaiYi-Xuan WangShi-Ao TongGang DengShenqi ZhangQian-Xue ChenPublished in: Medical oncology (Northwood, London, England) (2022)
Transmembrane and coiled-coil domains 1 (TMCO1) is a recently discovered transmembrane protein of endoplasmic reticulum (ER), which plays a critical role in maintaining calcium homeostasis. TMCO1 dysfunction has been proved to be closely related to a variety of human diseases, including glaucoma, deformities, mental retardation and tumorigenesis. However, the role of TMCO1 in gliomas remains unclear. The purpose of this study was to detect the role of TMCO1 in the pathogenesis and progression of gliomas. This study demonstrated that TMCO1 was upregulated in gliomas and its overexpression predicted poor prognosis. We also revealed that the expression of TMCO1 was associated with the World Health Organization (WHO) grade of gliomas. Knockdown of TMCO1 inhibited the proliferation and induced apoptosis of U87 and U251 cells. In addition, TMCO1 induced GBM cell migration and invasion by promoting epithelial-mesenchymal transition (EMT). These date collectively proved the crucial role of TMCO1 as a novel prognostic factor and underlying therapeutic target for glioma patients.
Keyphrases
- poor prognosis
- induced apoptosis
- high grade
- epithelial mesenchymal transition
- prognostic factors
- cell proliferation
- signaling pathway
- endoplasmic reticulum
- long non coding rna
- endothelial cells
- endoplasmic reticulum stress
- oxidative stress
- stem cells
- ejection fraction
- single cell
- mental health
- newly diagnosed
- induced pluripotent stem cells
- high glucose
- drug induced
- chronic kidney disease
- small molecule
- diabetic rats
- amino acid
- pluripotent stem cells
- cell cycle
- stress induced
- optic nerve