Department of Orthopedics, The Central Hospital of Wuhan, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430016, China.
Acta Biochim Pol. 2021 Oct 25;68(4):725-732. doi: 10.18388/abp.2020_5631.
MicroRNA (miR)-21 has been found to be overexpressed in osteosarcoma (OS). The aim of the present study was to investigate the effect of miR-21-5p on the Warburg effect and stemness maintenance in OS cells and its potential molecular mechanism. Herein, miR-21-5p was overexpressed or inhibited in MG-63 cells via transfection with mimics or inhibitors. The effect of miR-21-5p on cell viability, apoptosis, Warburg effect and stemness maintenance were explored in OS cells. The results demonstrated that miR-21-5p inhibition suppressed MG-63 cell viability and enhanced their apoptosis. Additionally, miR-21-5p inhibition attenuated the stemness maintenance of MG-63 cells, as demonstrated by the reduced proportion of CD133-positive MG-63 cells, the decrease in tumorsphere formation capacity, and the downregulation of Sox2, Oct4, and Nanog proteins. Moreover, miR-21-5p inhibition suppressed the Warburg effect in MG-63 cells, as indicated by the decrease in glucose uptake, lactic acid production, and ATP level and the downregulation of proteins involved in the Warburg effect (GLUT1, LDHA, HK2, and PKM2). Furthermore, the results suggested that the effect of miR-21-5p suppression on stemness and the Warburg effect may be associated with the decreased activity of the Wnt/β-catenin pathway in OS cells. Our findings suggest a novel potential biomarker for OS therapy.
微小 RNA(miR)-21 在骨肉瘤(OS)中被发现过度表达。本研究旨在探讨 miR-21-5p 对 OS 细胞的瓦伯格效应和干性维持的影响及其潜在的分子机制。在此,通过转染 mimics 或抑制剂,在 MG-63 细胞中过表达或抑制 miR-21-5p。探讨 miR-21-5p 对 OS 细胞活力、凋亡、瓦伯格效应和干性维持的影响。结果表明,miR-21-5p 抑制抑制 MG-63 细胞活力并增强其凋亡。此外,miR-21-5p 抑制降低了 MG-63 细胞的干性维持,表现为 CD133 阳性 MG-63 细胞的比例降低、肿瘤球形成能力下降以及 Sox2、Oct4 和 Nanog 蛋白表达下调。此外,miR-21-5p 抑制抑制了 MG-63 细胞的瓦伯格效应,表现为葡萄糖摄取、乳酸生成和 ATP 水平降低以及瓦伯格效应相关蛋白(GLUT1、LDHA、HK2 和 PKM2)表达下调。此外,结果表明 miR-21-5p 抑制对干性和瓦伯格效应的影响可能与 OS 细胞中 Wnt/β-catenin 通路活性降低有关。我们的研究结果为 OS 治疗提供了一个新的潜在生物标志物。