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1.广西医科大学基础医学院组织学与胚胎学教研室,广西 南宁 530021
2.广西医学科学院·广西壮族自治区人民医院颅脑肿瘤创伤功能神经外科,广西 南宁 530021
谢小薰,E-mail:xiaoxunxie59@foxmail.com
李希圣,E-mail:lxssky@hotmail.com
纸质出版日期:2025-02-25,
收稿日期:2024-03-16,
移动端阅览
梁国, 赵振凯, 曾曌月, 等. miR-330-5p靶向调控OY-TES-1抑制胶质母细胞瘤的迁移[J]. 局解手术学杂志, 2025,34(2):98-103.
LIANG GUO, ZHAO ZHEN-KAI, ZENG ZHAO-YUE, et al. MiR-330-5p targets OY-TES-1 to inhibit the migration of glioblastoma. [J]. Journal of regional anatomy and operative surgery, 2025, 34(2): 98-103.
梁国, 赵振凯, 曾曌月, 等. miR-330-5p靶向调控OY-TES-1抑制胶质母细胞瘤的迁移[J]. 局解手术学杂志, 2025,34(2):98-103. DOI: 10.11659/jjssx.03E024085.
LIANG GUO, ZHAO ZHEN-KAI, ZENG ZHAO-YUE, et al. MiR-330-5p targets OY-TES-1 to inhibit the migration of glioblastoma. [J]. Journal of regional anatomy and operative surgery, 2025, 34(2): 98-103. DOI: 10.11659/jjssx.03E024085.
目的
2
探究胶质母细胞瘤中miR-330-5p对OY-TES-1的靶向调控关系以及miR-330-5p/OY-TES-1轴对胶质母细胞瘤的迁移能力的影响。
方法
2
生物信息学分析胶质母细胞瘤患者中miR-330-5p的表达水平及其对患者预后生存的影响。将胶质母细胞瘤细胞U251分为miR-330-5p minics组、minics-NC组和miR-330-5p+OY-TES-1过表达组(miR-330-5p minics+pcDNA3.1-OY-TES-1)。使用双荧光素酶报告基因实验检测miR-330-5p对OY-TES-1 3'UTR区域活性的影响;使用qRT-PCR检测OY-TES-1 mRNA表达;采用Transwell迁移实验检测miR-330-5p/OY-TES-1轴对胶质母细胞瘤细胞迁移能力的影响。
结果
2
胶质母细胞瘤组织中miR-330-5p的表达明显低于非瘤脑组织和低级别胶质瘤组织(
P
<
0.05)。高表达miR-330-5p的胶质母细胞瘤患者生存期显著长于低表达miR-330-5p患者(
P
<
0.05)。过表达miR-330-5p后OY-TES-1 3'UTR区域活性下降
(P
<
0.05)。与minics-NC组相比,miR-330-5p minics组U251和U87MG细胞中OY-TES-1 mRNA表达水平显著降低(
P
<
0.01)。与minics-NC组相比,miR-330-5p minics组及miR-330-5p+OY-TES-1过表达组迁移细胞数显著减少(
P
<
0.05);与miR-330-5p minics组相比,miR-330-5p+OY-TES-1过表达组迁移细胞数显著增加(
P
<
0.01)。
结论
2
miR-330-5p靶向调控OY-TES-1抑制胶质母细胞瘤的迁移。
Objective
2
To explore the targeted regulatory relationship of miR-330-5p on OY-TES-1 in glioblastoma and the effect of miR-330-5p/OY-TES-1 axis on the migration ability of glioblastoma.
Methods
2
Bioinformatics analysis was performed to analyze the expression level of miR-330-5p in patients with glioblastoma and its influence on prognosis and survival of patients. The glioblastoma cells U251 were divided into miR-330-5p minics group, minics-NC group, and miR-330-5p+OY-TES-1 overexpression group (miR-330-5p minics+pcDNA3.1-OY-TES-1). The effect of miR-330-5p on the activity of OY-TES-1 3'UTR region was detected by double luciferase reporter gene experiment. The expression of OY-TES-1 mRNA was detected by qRT-PCR. The effect of miR-330-5p/OY-TES-1 axis on the migration ability of glioblastoma cells was detected by Transwell migration assay.
Results
2
The expression of miR-330-5p in glioblastoma tissue was significant
ly lower than those in non-tumor brain tissue and low-grade glioma tissue (
P
<
0.05). The survival time of glioblastoma patients with high expression of miR-330-5p was significantly longer than that of patients with low expression of miR-330-5p (
P
<
0.05). After overexpression of miR-330-5p, the activity of OY-TES-1 3'UTR region was decreased (
P
<
0.05). Compared with minics-NC group, the expression levels of OY-TES-1 mRNA of U251 and U87MG cells in miR-330-5p minics group were significantly decreased (
P
<
0.01). Compared with minics-NC group, the numbers of migrating cells in miR-330-5p minics group and miR-330-5p+OY-TES-1 overexpression group were significantly decreased (
P
<
0.05). Compared with miR-330-5p minics group, the number of migrating cells in miR-330-5p+OY-TES-1 overexpression group was significantly increased (
P
<
0.01).
Conclusion
2
MiR-330-5p targets OY-TES-1 to inhibit the migration of glioblastoma.
miR-330-5pOY-TES-1胶质母细胞瘤细胞迁移
miR-330-5pOY-TES-1glioblastomacell migration
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