Liang Rui, Zhang Guofeng, Xu Wenhua, Liu Weibing, Tang Youjia
Department of Neurosurgery, The First Hospital of Jiujiang City, Jiujiang, Jiangxi 332000, China.
Evid Based Complement Alternat Med. 2022 Aug 22;2022:5261285. doi: 10.1155/2022/5261285. eCollection 2022.
This work aims to investigate the effects of tetramethylpyrazine (TMP) on the proliferation, migration, and invasion of glioma cells and to analyze the regulation mechanism of TMP on the long noncoding RNA UBL7-AS1/miR-144-3p pathway. Glioma cell line and normal astrocytes were collected. The expression of UBL7-AS1 was detected by real-time PCR. The glioma cells were overexpressed with UBL7-AS1. CCK-8 and Transwell assays were used to detect cell proliferation and cell invasion ability, respectively. Bioinformatics was adopted to predict the possible regulatory mechanisms of UBL7-AS1. The dual luciferase reporter gene was applied to verify the regulatory effect of RNA UBL7-AS1 with miR-144-3p. TMP inhibited the proliferation and invasion of glioma cells. UBL7-AS1 was highly expressed in glioma tissues and cells. The overexpression of UBL7-AS1 promotes the cell proliferation and invasion of glioma. UBL7-AS1 can act as a sponge for miR-144-3p in glioma cells. The overexpression of UBL7-AS1 can reverse the inhibition of TMP on proliferation, migration, and invasion of glioma cells. TMP inhibits the proliferation, migration, and invasion of glioma cells by regulating the UBL7-AS1/miR-144-3p pathway.
本研究旨在探讨川芎嗪(TMP)对胶质瘤细胞增殖、迁移和侵袭的影响,并分析TMP对长链非编码RNA UBL7-AS1/miR-144-3p通路的调控机制。收集胶质瘤细胞系和正常星形胶质细胞。采用实时PCR检测UBL7-AS1的表达。使胶质瘤细胞过表达UBL7-AS1。分别采用CCK-8和Transwell实验检测细胞增殖和细胞侵袭能力。采用生物信息学预测UBL7-AS1可能的调控机制。应用双荧光素酶报告基因验证RNA UBL7-AS1与miR-144-3p的调控作用。TMP抑制胶质瘤细胞的增殖和侵袭。UBL7-AS1在胶质瘤组织和细胞中高表达。UBL7-AS1的过表达促进胶质瘤细胞的增殖和侵袭。UBL7-AS1在胶质瘤细胞中可作为miR-144-3p的海绵。UBL7-AS1的过表达可逆转TMP对胶质瘤细胞增殖、迁移和侵袭的抑制作用。TMP通过调控UBL7-AS1/miR-144-3p通路抑制胶质瘤细胞的增殖、迁移和侵袭。