基因敲除
生物
下调和上调
基因沉默
细胞生长
核糖核酸
癌症研究
RNA干扰
细胞凋亡
基因
细胞
长非编码RNA
遗传学
作者
Shun Ke,Jing Wang,Lu Jun,Minghao Fang,Ruichao Li
出处
期刊:Genomics
[Elsevier BV]
日期:2023-03-01
卷期号:115 (3): 110593-110593
被引量:6
标识
DOI:10.1016/j.ygeno.2023.110593
摘要
We aimed at probing impact of LINC00858 on esophageal squamous cell carcinoma (ESCC) progression via ZNF184-FTO-m6A-MYC axis.Expression of related genes (LINC00858, ZNF184, FTO, and MYC) was detected in ESCC tissues or cells and their relationships were assessed. After expression alterations in ESCC cells, cell proliferation, invasion, migration, and apoptosis were detected. Tumor formation in nude mice was conducted.LINC00858, ZNF184, FTO, and MYC were overexpressed in ESCC tissues and cells. LINC00858 enhanced ZNF184 expression to upregulate FTO, which augmented MYC expression. LINC00858 knockdown diminished ESCC cell proliferative, migratory, and invasive properties while elevating apoptosis, which was negated by FTO overexpression. FTO knockdown exerted similar functions of LINC00858 knockdown on ESCC cell movements, which was annulled by MYC upregulation. Silencing LINC00858 repressed tumor growth and related gene expression in nude mice.LINC00858 modulated MYC m6A modification via FTO by recruiting ZNF184, thus facilitating ESCC progression.
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