Department of Orthopaedics, Minhang Hospital, Fudan University, 170 Xin-Song Road, Shanghai 201199, China.
Comput Math Methods Med. 2020 Sep 9;2020:7236245. doi: 10.1155/2020/7236245. eCollection 2020.
Long noncoding RNAs (lncRNAs) played a crucial role in a number of biological processes. lncRNA HAGLROS was demonstrated to facilitate cell proliferation and migration in various cancers. However, the functions and molecular mechanisms of HAGLROS in osteosarcoma remained to be elucidated.
qRT-PCR assay was used to detect the relative expression of HAGLROS in osteosarcoma tissue samples and cells. CCK-8 and Transwell assays were performed to assess the effects of HAGLROS on OS cells proliferation and invasion. Luciferase reporter assay verified the interaction between ROCK1 and miR-152.
In our study, we found that the expression of HAGLROS increased osteosarcoma samples and cell lines compared with normal tissues and cells. HAGLROS knockdown inhibited certain functions of U2OS and SW1353 cells in vitro. Moreover, HAGLROS depletion inhibited tumor growth and metastasis in vivo. Mechanically, we found that HAGLROS sponged miR-152 to promote ROCK1 expression in U2OS and SW1353 cells.
In summary, our study indicated that HAGLROS could promote osteosarcoma progression by sponging miR-152 to promote ROCK1 expression. The results showed HAGLROS/miR-152/ROCK1 axis might act as a novel therapeutic strategy for osteosarcoma.
长链非编码 RNA(lncRNA)在许多生物学过程中发挥着关键作用。lncRNA HAGLROS 被证明可促进多种癌症中的细胞增殖和迁移。然而,HAGLROS 在骨肉瘤中的功能和分子机制仍有待阐明。
qRT-PCR 检测骨肉瘤组织样本和细胞中 HAGLROS 的相对表达。CCK-8 和 Transwell 检测用于评估 HAGLROS 对 OS 细胞增殖和侵袭的影响。荧光素酶报告实验验证了 ROCK1 和 miR-152 之间的相互作用。
在本研究中,我们发现 HAGLROS 在骨肉瘤样本和细胞系中的表达高于正常组织和细胞。HAGLROS 敲低抑制了 U2OS 和 SW1353 细胞在体外的某些功能。此外,HAGLROS 耗竭抑制了体内肿瘤的生长和转移。从机制上讲,我们发现 HAGLROS 可通过海绵吸附 miR-152 促进 U2OS 和 SW1353 细胞中的 ROCK1 表达。
综上所述,本研究表明 HAGLROS 可通过海绵吸附 miR-152 促进 ROCK1 表达来促进骨肉瘤的进展。结果表明 HAGLROS/miR-152/ROCK1 轴可能成为骨肉瘤的一种新的治疗策略。