circNDUFB2 inhibits non-small cell lung cancer progression via destabilizing IGF2BPs and activating anti-tumor immunity

Botai Li(Shanghai Jiao Tong University), Lili Zhu(Shanghai Jiao Tong University), Chunlai Lu(Sun Yat-sen University), Cun Wang(Shanghai Jiao Tong University), Hui Wang(Shanghai Jiao Tong University), Haojie Jin(Shanghai Jiao Tong University), Xuhui Ma(Shanghai Jiao Tong University), Zhuoan Cheng(Shanghai Jiao Tong University), Chengtao Yu(Shanghai Jiao Tong University), Siying Wang(Shanghai Jiao Tong University), Qiaozhu Zuo(Shanghai Jiao Tong University), Yangyang Zhou(Shanghai Jiao Tong University), Jun Wang(Shanghai Jiao Tong University), Chen Yang(Shanghai Jiao Tong University), Yuanyuan Lv(Shanghai Jiao Tong University), Liyan Jiang(Shanghai Jiao Tong University), Wenxin Qin(Shanghai Jiao Tong University)
Nature Communications
January 12, 2021
Cited by 858Open Access
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Abstract

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 N 6 -methyladenosine (m 6 A) 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.


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