内质网
核糖核酸
生物
转移
结直肠癌
癌症研究
细胞生物学
癌症
基因
遗传学
作者
Shuyang Wang,Lingjie Zhang,Guojun Chen,Qi-Qi Ni,Yuan Huang,Dan Zhang,Fangyi Han,Wenfeng He,Li-ling He,Yanqing Ding,Hong‐Li Jiao,Yaping Ye
出处
期刊:Cancer Letters
[Elsevier]
日期:2022-11-04
卷期号:553: 215995-215995
被引量:6
标识
DOI:10.1016/j.canlet.2022.215995
摘要
RNA editing is among the most common RNA level modifications for generating amino acid changes. We identified a COPA A-to-I RNA editing event in CRC metastasis. Our results showed that the COPA A-to-I RNA editing rate was significantly increased in metastatic CRC tissues and was closely associated with aggressive tumors in the T and N stages. The COPA I164V protein damaged the Golgi–ER reverse transport function, induced ER stress, promoted the translocation of the transcription factors ATF6, XBP1 and ATF4 into the nucleus, and activated the expression of MALAT1, MET, ZEB1, and lead to CRC cell invasion and metastasis. Moreover, the COPA A-to-I RNA editing rate was positively correlated with the immune infiltration score. Collectively, the COPA I164V protein hijacked ER stress to promote the metastasis of CRC, and the COPA A-to-I RNA editing rate may be a potential predictor for patient response to immune checkpoint inhibitor (ICIs) treatment.
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