转录组
竞争性内源性RNA
生物
N6-甲基腺苷
甲基化
小RNA
癌症研究
DNA甲基化
核糖核酸
微阵列分析技术
RNA甲基化
基因表达
基因
细胞
微阵列
平铺阵列
细胞生物学
遗传学
长非编码RNA
甲基转移酶
作者
Xiaoli Jia,Zhilong Zhang,Rongqiang Wei,Bin Li,Yiyang Chen,Jiang Li
标识
DOI:10.1016/j.prp.2022.154055
摘要
N6-Methyladenosine (m6A) RNA methylation is the most prevalent post-transcriptional modification mechanism in humans and plays an important role in the pathogenesis of various tumors. However, the investigation of m6A modification in Esophageal squamous cell carcinoma (ESCC) remains in its infancy. Transcriptome-wide m6A changes were profiled using human m6A epitranscriptomic microarrays in ESCC tissues and adjacent normal tissues. Differentially m6A-methylated mRNAs, lncRNAs and Mid-size ncRNAs were identified, followed by functional enrichment analysis. Moreover, we also establish a competing endogenous RNA (ceRNA) network based on the m6A-related lncRNA growth arrest specific 5 (GAS5) specific transcript(NR_152533). The results suggested that RALYL may be a target gene for miR-3912-5p, and that GAS5 regulated RALYL expression by binding to miR-3912-5p.
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