小核仁RNA
甲基化
自噬
转移
癌症研究
长非编码RNA
生物
肺癌
细胞生长
PI3K/AKT/mTOR通路
DNA甲基化
核糖体RNA
细胞生物学
癌症
核糖核酸
基因
基因表达
信号转导
细胞凋亡
遗传学
医学
肿瘤科
作者
Kangyu Wang,Shiwen Wang,Yue Zhang,Li Xie,Xingguo Song,Xianrang Song
标识
DOI:10.1038/s41418-022-01087-9
摘要
Small nucleolar RNAs (snoRNAs) have been shown to play critical regulatory roles in cancer development. SNORD88C, which located at the intronic region of C19orf48 in chromosome 19q.33 with a 97-nt length was screened through database and snoRNA-sequencing. We firstly verified this snoRNA was up-regulated in tissue and plasma and served as a non-invasive diagnostic biomarker; then confirmed that SNORD88C promoted proliferation and metastasis of NSCLC in vitro and in vivo. Mechanistically, SNORD88C promoted 2′-O-methylation modification at the C3680 site on 28S rRNA and in turn enhanced downstream SCD1 translation, a central lipogenic enzyme for the synthesis of MUFA that can inhibit autophagy by regulating lipid peroxidation and mTOR, providing the novel insight into the regulation of SNORD88C in NSCLC.
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