{"title":"Piezo1-related physiological and pathological processes in glioblastoma.","authors":"Weijia Fu, Xue Hou, Lijuan Ding, Jiaying Wei, Wei Hou","doi":"10.3389/fcell.2025.1536320","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Glioblastoma (GBM) is the most malignant of the astrocytomas, primarily involving the cerebral hemispheres and cerebral cortex. It is one of the fatal refractory solid tumors with a 5-year survival rate of only 5% in adults. Cells in biological tissues are subjected to mechanical forces, including hydrostatic pressure, shear stress, compression and tension. Cells can convert mechanomechanical signals into biological or electrical signals, a process known as mechanical signaling. Piezo1 channels, members of the Piezo family of mechanosensitive ion channels, can be directly activated by mechanical stimuli alone, mediating mechanosensitive cation currents that activate subsequent signaling pathways. Studies have shown that Piezo1 is largely unexpressed in normal brain tissues but is expressed at high levels in glioblastoma and can significantly contribute to glioblastoma development and progression, but its role in the pathogenesis of glioblastoma remains unclear.</p><p><strong>Methods: </strong>We reviewed the relevant literature and data in six major databases including PubMed, EMBASE, CINAHL, Scopus, Web of Science and TCGA. Finally, a total of 126 papers were selected for review and analysis (Search terms include: glioblastoma, piezo1, biomechanical, targeted therapy, mechanomechanical, extracellular matrix, radiation therapy and more). The role of piezo1 in the development of glioblastoma was summarized.</p><p><strong>Results: </strong>Piezo1 affects several fundamental pathophysiological processes in glioblastoma, such as tissue sclerosis, angiogenesis, energy supply, and immune cell infiltration, and can be used as an indicator of malignancy and prognosis in patients with glioblastoma, as well as a therapeutic target to control tumor progression.</p><p><strong>Discussion: </strong>The pathological mechanism of piezo1 in glioblastoma is very complex, and the aberrant expression of piezo1 plays a very important role in the development of glioblastoma. Specific mechanistic studies focusing on Piezo1 will help us understand the mechanobiology of glioblastoma and help us develop new therapeutic approaches for glioblastoma patients.</p>","PeriodicalId":12448,"journal":{"name":"Frontiers in Cell and Developmental Biology","volume":"13 ","pages":"1536320"},"PeriodicalIF":4.6000,"publicationDate":"2025-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11885286/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in Cell and Developmental Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.3389/fcell.2025.1536320","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Introduction: Glioblastoma (GBM) is the most malignant of the astrocytomas, primarily involving the cerebral hemispheres and cerebral cortex. It is one of the fatal refractory solid tumors with a 5-year survival rate of only 5% in adults. Cells in biological tissues are subjected to mechanical forces, including hydrostatic pressure, shear stress, compression and tension. Cells can convert mechanomechanical signals into biological or electrical signals, a process known as mechanical signaling. Piezo1 channels, members of the Piezo family of mechanosensitive ion channels, can be directly activated by mechanical stimuli alone, mediating mechanosensitive cation currents that activate subsequent signaling pathways. Studies have shown that Piezo1 is largely unexpressed in normal brain tissues but is expressed at high levels in glioblastoma and can significantly contribute to glioblastoma development and progression, but its role in the pathogenesis of glioblastoma remains unclear.
Methods: We reviewed the relevant literature and data in six major databases including PubMed, EMBASE, CINAHL, Scopus, Web of Science and TCGA. Finally, a total of 126 papers were selected for review and analysis (Search terms include: glioblastoma, piezo1, biomechanical, targeted therapy, mechanomechanical, extracellular matrix, radiation therapy and more). The role of piezo1 in the development of glioblastoma was summarized.
Results: Piezo1 affects several fundamental pathophysiological processes in glioblastoma, such as tissue sclerosis, angiogenesis, energy supply, and immune cell infiltration, and can be used as an indicator of malignancy and prognosis in patients with glioblastoma, as well as a therapeutic target to control tumor progression.
Discussion: The pathological mechanism of piezo1 in glioblastoma is very complex, and the aberrant expression of piezo1 plays a very important role in the development of glioblastoma. Specific mechanistic studies focusing on Piezo1 will help us understand the mechanobiology of glioblastoma and help us develop new therapeutic approaches for glioblastoma patients.
胶质母细胞瘤(GBM)是最恶性的星形细胞瘤,主要累及大脑半球和大脑皮层。它是一种致命的难治性实体瘤,成人5年生存率仅为5%。生物组织中的细胞受到机械力的作用,包括静水压力、剪切应力、压缩和张力。细胞可以将机械机械信号转化为生物或电子信号,这一过程被称为机械信号。Piezo1通道是机械敏感离子通道压电家族的成员,可以通过机械刺激直接激活,介导机械敏感阳离子电流激活随后的信号通路。研究表明,Piezo1在正常脑组织中基本不表达,但在胶质母细胞瘤中高水平表达,可以显著促进胶质母细胞瘤的发生和进展,但其在胶质母细胞瘤发病机制中的作用尚不清楚。方法:检索PubMed、EMBASE、CINAHL、Scopus、Web of Science、TCGA六大数据库的相关文献和数据。最后,共选取126篇论文进行综述和分析(检索词包括:胶质母细胞瘤、压电、生物力学、靶向治疗、机械力学、细胞外基质、放射治疗等)。综述了piezo1在胶质母细胞瘤发生发展中的作用。结果:Piezo1影响胶质母细胞瘤组织硬化、血管生成、能量供应、免疫细胞浸润等基本病理生理过程,可作为胶质母细胞瘤患者恶性程度和预后的指标,也是控制肿瘤进展的治疗靶点。讨论:piezo1在胶质母细胞瘤中的病理机制非常复杂,piezo1的异常表达在胶质母细胞瘤的发生发展中起着非常重要的作用。以Piezo1为重点的具体机制研究将有助于我们了解胶质母细胞瘤的力学生物学,并帮助我们为胶质母细胞瘤患者开发新的治疗方法。
期刊介绍:
Frontiers in Cell and Developmental Biology is a broad-scope, interdisciplinary open-access journal, focusing on the fundamental processes of life, led by Prof Amanda Fisher and supported by a geographically diverse, high-quality editorial board.
The journal welcomes submissions on a wide spectrum of cell and developmental biology, covering intracellular and extracellular dynamics, with sections focusing on signaling, adhesion, migration, cell death and survival and membrane trafficking. Additionally, the journal offers sections dedicated to the cutting edge of fundamental and translational research in molecular medicine and stem cell biology.
With a collaborative, rigorous and transparent peer-review, the journal produces the highest scientific quality in both fundamental and applied research, and advanced article level metrics measure the real-time impact and influence of each publication.