Department of Microrepair and Reconstruction, the First Affiliated Hospital of Xinjiang Medical University, Xinjiang, P.R China.
Department of Operation Room, the First Affiliated Hospital of Xinjiang Medical University, Xinjiang, P.R China.
J Recept Signal Transduct Res. 2022 Feb;42(1):71-79. doi: 10.1080/10799893.2020.1850784. Epub 2020 Dec 6.
Osteosarcoma (OS), a prevalent aggressive malignancy in the bone, has limited therapeutic targets and diagnostic biomarkers. In the current investigation, RT-qPCR showed that CDKN2B-AS1 was enhanced in OS samples and cells. This research was set to examine the modulation of CDKN2B-AS1 in OS. The expression of CDKN2B-AS1 and downstream molecules was analyzed by RT-qPCR method. CCK8, EdU staining along with Transwell assays were applied to evaluate cell proliferation and invasion. Those investigations specified that silencing of CDKN2B-AS1 with shRNAs obviously impeded the proliferation and invasion of MG63 cells. To authenticate the relationships between CDKN2B-AS1 and microRNA-122-5p (miR-122-5p) or cyclin G1 (CCNG1) and miR-122-5p, we next employed luciferase reporter assay. We displayed that CDKN2B-AS1 repressed miR-122-5p to restore CCNG1 expression. All in all, our findings substantiated the indispensable function of CDKN2B-AS1 in OS progression and the possible molecular mechanism.
骨肉瘤(OS)是一种常见的侵袭性骨恶性肿瘤,其治疗靶点和诊断生物标志物有限。在本研究中,实时定量 PCR 显示 CDKN2B-AS1 在 OS 样本和细胞中增强。本研究旨在研究 CDKN2B-AS1 在 OS 中的调节作用。通过 RT-qPCR 方法分析 CDKN2B-AS1 和下游分子的表达。CCK8、EdU 染色和 Transwell 实验用于评估细胞增殖和侵袭。这些研究表明,shRNA 沉默 CDKN2B-AS1 明显抑制了 MG63 细胞的增殖和侵袭。为了验证 CDKN2B-AS1 与 microRNA-122-5p(miR-122-5p)或细胞周期蛋白 G1(CCNG1)和 miR-122-5p 之间的关系,我们接下来进行了荧光素酶报告基因实验。我们显示 CDKN2B-AS1 通过抑制 miR-122-5p 来恢复 CCNG1 的表达。总之,我们的研究结果证实了 CDKN2B-AS1 在 OS 进展中的重要作用及其可能的分子机制。