下调和上调
胶质母细胞瘤
细胞生长
癌症研究
U87型
小RNA
生物
C-Met公司
细胞生物学
神经科学
细胞培养
基因
受体
肝细胞生长因子
遗传学
作者
Xiaojiao Wang,Wei Tian,Liang Wu,Zhenqing Wei,Weihua Li,Yousong Xu,Li Yang
出处
期刊:Neuroreport
[Ovid Technologies (Wolters Kluwer)]
日期:2020-06-10
卷期号:31 (9): 657-662
被引量:9
标识
DOI:10.1097/wnr.0000000000001469
摘要
LncRNA SNHG4 has been reported to be an oncogenic lncRNA in osteosarcoma. Our preliminary analysis of the cancer genome atlas dataset revealed the upregulation of SNHG4 in glioblastoma (GBM). In this study, we confirmed the upregulation of SNHG4 in GBM tissues collected from GBM patients. In addition, lower survival rate of GBM patients was observed in patients with high SNHG4 expression level. SNHG4 can directly interact with miR-138, while SNHG4 expression was no altered after miR-138 overexpression. Interestingly, SNHG4 overexpression led to the upregulation of c-Met, a target of miR-138. Cell counting kit-8 assay showed that miR-138 overexpression resulted in decreased proliferation rate of GBM cells. SNHG4 and c-Met overexpression played opposite roles and reduced the effects of miR-138. Therefore, SNHG4 regulates miR-138/c-Met axis to promote the proliferation of GBM cells.
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