Fischell Department of Bioengineering, University of Maryland, 3110 A. James Clark Hall, 8278 Paint Branch Drive, College Park, MD, 20742, USA.
Marlene and Stewart Greenebaum Comprehensive Cancer Center, University of Maryland, Baltimore, MD, 21201, USA.
Cell Mol Life Sci. 2023 Jan 22;80(2):48. doi: 10.1007/s00018-022-04665-9.
Dysregulated cell migration and invasion are hallmarks of many disease states. This dysregulated migratory behavior is influenced by the changes in expression of aquaporins (AQPs) that occur during pathogenesis, including conditions such as cancer, endometriosis, and arthritis. The ubiquitous function of AQPs in migration of diseased cells makes them a crucial target for potential therapeutics; this possibility has led to extensive research into the specific mechanisms underlying AQP-mediated diseased cell migration. The functions of AQPs depend on a diverse set of variables including cell type, AQP isoform, disease state, cell microenvironments, and even the subcellular localization of AQPs. To consolidate the considerable work that has been conducted across these numerous variables, here we summarize and review the last decade's research covering the role of AQPs in the migration and invasion of cells in diseased states.
细胞迁移和侵袭失调是许多疾病状态的特征。这种失调的迁移行为受 Aquaporins(AQPs)表达变化的影响,这些变化发生在发病过程中,包括癌症、子宫内膜异位症和关节炎等疾病。AQPs 在病变细胞迁移中的普遍功能使其成为潜在治疗药物的关键靶点;这一可能性促使人们对 AQP 介导的病变细胞迁移的具体机制进行了广泛的研究。AQPs 的功能取决于一系列不同的变量,包括细胞类型、AQP 同工型、疾病状态、细胞微环境,甚至 AQPs 的亚细胞定位。为了整合在这些众多变量中进行的大量工作,我们在这里总结和回顾了过去十年的研究,涵盖了 AQPs 在病变状态下细胞迁移和侵袭中的作用。