Harich Octavia-Oana, Gavriliuc Oana-Isabella, Ordodi Valentin-Laurentiu, Tirziu Alexandru, Paunescu Virgil, Panaitescu Carmen, Bojin Maria-Florina
Department of Functional Sciences, Immuno-Physiology and Biotechnologies Center, "Victor Babes" University of Medicine and Pharmacy, No. 2 Eftimie Murgu Square, 300041 Timisoara, Romania.
Faculty of Industrial Chemistry and Environmental Engineering, "Politehnica" University Timisoara, No 2 Victoriei Square, 300006 Timisoara, Romania.
Biomedicines. 2023 Aug 5;11(8):2205. doi: 10.3390/biomedicines11082205.
Na/K ATPase is a protein involved in the active transport of ions across the cellular membrane. Ouabain is a cardiotonic glycoside that, by inhibiting the Na/K pump, interferes with cell processes mediated directly by the pump, but also indirectly influences other cellular processes such as cell cycle and proliferation, growth, cell differentiation, angiogenesis, migration, adhesion, and invasion. We used the SK-BR-3 breast cancer cell line, mesenchymal stem cells (MSCs), and tumor-associated fibroblasts (TAFs) in vitro to determine the effects of ouabain exposure on these cellular types. The results showed a multi-level effect of ouabain mainly on tumor cells, in a dose-dependent manner, while the TAFs and their normal counterparts were not significantly influenced. Following exposure to ouabain, the SK-BR-3 cells changed their morphologic appearance, decreased the expression of immunophenotypic markers (CD29, Her2, VEGF), the proliferation rate was significantly decreased (Ki67 index), the cells were blocked in the G phase of the cell cycle and suffered necrosis. These data were correlated with the variable expression of α and β Na/K pump subunits in tumor cells, resulting in decreased ability to adhere to the VCAM-1 substrate in functional flow chamber studies. Being indicative of the pro-apoptotic and inhibitory effect of ouabain on tumor invasion and metastasis, the results support the addition of ouabain to the oncological therapeutic arsenal, trailing the "repurposing drugs" approach.
钠钾ATP酶是一种参与离子跨细胞膜主动转运的蛋白质。哇巴因是一种强心苷,它通过抑制钠钾泵,不仅干扰由该泵直接介导的细胞过程,还间接影响其他细胞过程,如细胞周期、增殖、生长、细胞分化、血管生成、迁移、黏附和侵袭。我们在体外使用SK-BR-3乳腺癌细胞系、间充质干细胞(MSC)和肿瘤相关成纤维细胞(TAF)来确定哇巴因暴露对这些细胞类型的影响。结果显示,哇巴因主要对肿瘤细胞有多层次的影响,且呈剂量依赖性,而TAF及其正常对应物未受到显著影响。暴露于哇巴因后,SK-BR-3细胞改变了形态外观,免疫表型标志物(CD29、Her2、VEGF)的表达降低,增殖率显著下降(Ki67指数),细胞在细胞周期的G期被阻滞并发生坏死。这些数据与肿瘤细胞中α和β钠钾泵亚基的可变表达相关,导致在功能性流动腔研究中细胞黏附于VCAM-1底物的能力下降。这些结果表明哇巴因对肿瘤侵袭和转移具有促凋亡和抑制作用,支持将哇巴因添加到肿瘤治疗药物库中,遵循“药物重新利用”的方法。