Sui Cong, Liu Debao, Hu Yong, Zhang Linlin
Department of Orthopedics, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui 230032, P.R. China.
Department of Orthopaedics, The First Affiliated Hospital of University of Science and Technology of China, Hefei, Anhui 230001, P.R. China.
Exp Ther Med. 2019 Mar;17(3):2235-2241. doi: 10.3892/etm.2019.7171. Epub 2019 Jan 15.
Osteosarcoma is an aggressive cancer of the skeletal system which remains a challenge for the current therapeutic strategies due to unclear etiology and molecular mechanisms of pathogenesis. The current study aimed to determine the expression levels, role and molecular mechanism of microRNA-708-5p (miR-708-5p) in the development of osteosarcoma. The expression level of miR-708-5p was detected using reverse transcription-quantitative polymerase chain reaction. miR-708-5p was overexpressed in SaOS-2 cells using miR-708-5p mimics. Cell viability, apoptosis, migration and invasion were determined using Cell Counting kit-8 assay, flow cytometry, wound healing and transwell assays, respectively. The results indicated that miR-708-5p was significantly downregulated in osteosarcoma tissues and cells, and its overexpression significantly inhibited cell viability, invasion and migration and induced apoptosis of SaOS-2 cells. Furthermore, the present results indicated that miR-708-5p directly targeted the 3'-untranslated region of up-regulator of cell proliferation (URGCP) and negatively regulated its expression in SaOS-2 cells. Taken together, the current study suggested that miR-708-5p may inhibit the growth and invasion of osteosarcoma cells via regulating the URGCP/NF-κB signaling pathway. Further research on these molecules in osteosarcoma may provide novel insights into the target therapy for this disease.
骨肉瘤是一种侵袭性的骨骼系统癌症,由于其发病原因和分子机制尚不清楚,目前的治疗策略仍面临挑战。本研究旨在确定微小RNA-708-5p(miR-708-5p)在骨肉瘤发生发展中的表达水平、作用及分子机制。采用逆转录-定量聚合酶链反应检测miR-708-5p的表达水平。使用miR-708-5p模拟物在SaOS-2细胞中过表达miR-708-5p。分别使用细胞计数试剂盒-8法、流式细胞术、伤口愈合试验和Transwell试验测定细胞活力、凋亡、迁移和侵袭能力。结果表明,miR-708-5p在骨肉瘤组织和细胞中显著下调,其过表达显著抑制SaOS-2细胞的活力、侵袭和迁移,并诱导其凋亡。此外,本研究结果表明,miR-708-5p直接靶向细胞增殖上调因子(URGCP)的3'-非翻译区,并在SaOS-2细胞中负调控其表达。综上所述,本研究提示miR-708-5p可能通过调节URGCP/NF-κB信号通路抑制骨肉瘤细胞的生长和侵袭。对骨肉瘤中这些分子的进一步研究可能为该疾病的靶向治疗提供新的见解。