癌变
结直肠癌
癌症研究
生物
免疫系统
肽
信号转导
癌症
机制(生物学)
细胞生物学
核糖核酸
免疫
长非编码RNA
打开阅读框
胞浆
DNA损伤
细胞信号
翻译(生物学)
小RNA
肽序列
磷酸化
线粒体
DNA
病态的
作者
Qi Wu,Zhun Li,Xinxin He,Shuhui Yu,Mengrou Zhang,Hui Mo,Saiqi He,Jianming Li,Wen Ni
出处
期刊:Carcinogenesis
[Oxford University Press]
日期:2025-12-16
卷期号:47 (1)
被引量:2
标识
DOI:10.1093/carcin/bgaf092
摘要
Long non-coding RNAs (lncRNAs) serve as pivotal regulators of diverse physiological activities through their interactions with different biomolecules, and their aberrant expression frequently contributes to tumorigenesis and malignant progression. Emerging evidence has demonstrated that certain lncRNAs contain open reading frames that can generate useful short peptides, which influence cancer-related physiological and pathological pathways via diverse mechanisms. In this research, we identified that the lncRNA LRRC75A-AS1 encodes a conserved peptide consisting of 102 amino acids, designated as LRRC75A-AS1-ORF3. Notably, this peptide acts independently of the non-coding RNA itself to suppress anti-tumor immune responses and promote colorectal cancer progression. Mechanistically, LRRC75A-AS1-ORF3 is localized in the mitochondria, where it induces mitophagy, thereby eliminating cytosolic mitochondrial DNA (mtDNA) and downregulating the cGAS-STING signaling pathway. Our findings reveal a previously uncharacterized mechanism by which LRRC75A-AS1-ORF3 impairs anti-tumor immunity, thereby presenting a novel immunotherapeutic target for colorectal cancer treatment.
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