Radiotherapy Center, Xi'an International Medical Center Hospital, Xi'an, Shaanxi Province, China 710100.
Department of Geriatric Endocrinology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi Province, China 710100.
Comput Math Methods Med. 2021 Oct 18;2021:7952922. doi: 10.1155/2021/7952922. eCollection 2021.
Far less has been unveiled about the functions of lncRNAs on cancers yet. Here, we reported that lncRNA FAM87A, as a ceRNA of miR-424-5p, played a vital role in glioma development. qRT-PCR result indicated that FAM87A was abnormally downregulated in glioma tissue and cells. Survival analysis suggested that the FAM87A expression was negatively correlated with the survival rate. Effects of FAM87A on human glioma cell lines were also analyzed by MTT, Edu, and transwell assays. FAM87A hastened proliferation and migration of glioma cells. MiR-424-5p, predicted target of FAM87A, was fostered in glioma, which was examined by qRT-PCR. A negative correlation was indicated between FAM87A and miR-424-5p. Results of bioinformatics, dual luciferase, and RIP assays unveiled that FAM87A and miR-424-5p act upon each other. In addition, miR-424-5p targeted 3'-UTR of PPM1H. Also, effects of miR-424-5p/FAM87A on glioma cells were identified via the cell function experiments. FAM87A suppressed PPM1H by binding to miR-424-5p competitively, thereby restraining cell proliferation, migration, and invasion. Collectively, these findings illuminated a new mechanism for glioma progression. Therefore, FAM87A may act as a feasible target for glioma treatment.
关于 lncRNAs 在癌症中的功能,人们了解得还很少。在这里,我们报道 lncRNA FAM87A 作为 miR-424-5p 的 ceRNA,在胶质瘤的发展中起着至关重要的作用。qRT-PCR 结果表明 FAM87A 在胶质瘤组织和细胞中异常下调。生存分析表明 FAM87A 的表达与存活率呈负相关。通过 MTT、Edu 和 Transwell 测定分析 FAM87A 对人胶质瘤细胞系的影响。FAM87A 加速了神经胶质瘤细胞的增殖和迁移。通过 qRT-PCR 检测到 miR-424-5p,即 FAM87A 的预测靶点,在神经胶质瘤中得到了促进。FAM87A 和 miR-424-5p 之间存在负相关。生物信息学、双荧光素酶和 RIP 测定的结果揭示了 FAM87A 和 miR-424-5p 相互作用。此外,miR-424-5p 靶向 PPM1H 的 3'-UTR。同样,通过细胞功能实验确定了 miR-424-5p/FAM87A 对神经胶质瘤细胞的影响。FAM87A 通过与 miR-424-5p 竞争结合来抑制 PPM1H,从而抑制细胞增殖、迁移和侵袭。综上所述,这些发现为胶质瘤的进展提供了一个新的机制。因此,FAM87A 可能成为治疗神经胶质瘤的一个可行靶点。