| Literature DB >> 33436560 |
Botai Li1, Lili Zhu1, Chunlai Lu2, Cun Wang3, Hui Wang3, Haojie Jin3, Xuhui Ma3, Zhuoan Cheng1, Chengtao Yu1, Siying Wang3, Qiaozhu Zuo3, Yangyang Zhou3, Jun Wang3, Chen Yang3, Yuanyuan Lv3, Liyan Jiang4, Wenxin Qin5,6.
Abstract
Circular RNAs (circRNA) are a class of covalently closed single-stranded RNAs that have been implicated in cancer progression. Here we identify circNDUFB2 to be downregulated in non-small cell lung cancer (NSCLC) tissues, and to negatively correlate with NSCLC malignant features. Elevated circNDUFB2 inhibits growth and metastasis of NSCLC cells. Mechanistically, circNDUFB2 functions as a scaffold to enhance the interaction between TRIM25 and IGF2BPs, a positive regulator of tumor progression and metastasis. This TRIM25/circNDUFB2/IGF2BPs ternary complex facilitates ubiquitination and degradation of IGF2BPs, with this effect enhanced by N6-methyladenosine (m6A) modification of circNDUFB2. Moreover, circNDUFB2 is also recognized by RIG-I to activate RIG-I-MAVS signaling cascades and recruit immune cells into the tumor microenvironment (TME). Our data thus provide evidences that circNDUFB2 participates in the degradation of IGF2BPs and activation of anti-tumor immunity during NSCLC progression via the modulation of both protein ubiquitination and degradation, as well as cellular immune responses.Entities:
Year: 2021 PMID: 33436560 DOI: 10.1038/s41467-020-20527-z
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919