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

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...

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Autores principales: Li, Botai, Zhu, Lili, Lu, Chunlai, Wang, Cun, Wang, Hui, Jin, Haojie, Ma, Xuhui, Cheng, Zhuoan, Yu, Chengtao, Wang, Siying, Zuo, Qiaozhu, Zhou, Yangyang, Wang, Jun, Yang, Chen, Lv, Yuanyuan, Jiang, Liyan, Qin, Wenxin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7804955/
https://www.ncbi.nlm.nih.gov/pubmed/33436560
http://dx.doi.org/10.1038/s41467-020-20527-z
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author Li, Botai
Zhu, Lili
Lu, Chunlai
Wang, Cun
Wang, Hui
Jin, Haojie
Ma, Xuhui
Cheng, Zhuoan
Yu, Chengtao
Wang, Siying
Zuo, Qiaozhu
Zhou, Yangyang
Wang, Jun
Yang, Chen
Lv, Yuanyuan
Jiang, Liyan
Qin, Wenxin
author_facet Li, Botai
Zhu, Lili
Lu, Chunlai
Wang, Cun
Wang, Hui
Jin, Haojie
Ma, Xuhui
Cheng, Zhuoan
Yu, Chengtao
Wang, Siying
Zuo, Qiaozhu
Zhou, Yangyang
Wang, Jun
Yang, Chen
Lv, Yuanyuan
Jiang, Liyan
Qin, Wenxin
author_sort Li, Botai
collection PubMed
description 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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spelling pubmed-78049552021-01-21 circNDUFB2 inhibits non-small cell lung cancer progression via destabilizing IGF2BPs and activating anti-tumor immunity Li, Botai Zhu, Lili Lu, Chunlai Wang, Cun Wang, Hui Jin, Haojie Ma, Xuhui Cheng, Zhuoan Yu, Chengtao Wang, Siying Zuo, Qiaozhu Zhou, Yangyang Wang, Jun Yang, Chen Lv, Yuanyuan Jiang, Liyan Qin, Wenxin Nat Commun Article 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. Nature Publishing Group UK 2021-01-12 /pmc/articles/PMC7804955/ /pubmed/33436560 http://dx.doi.org/10.1038/s41467-020-20527-z Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Li, Botai
Zhu, Lili
Lu, Chunlai
Wang, Cun
Wang, Hui
Jin, Haojie
Ma, Xuhui
Cheng, Zhuoan
Yu, Chengtao
Wang, Siying
Zuo, Qiaozhu
Zhou, Yangyang
Wang, Jun
Yang, Chen
Lv, Yuanyuan
Jiang, Liyan
Qin, Wenxin
circNDUFB2 inhibits non-small cell lung cancer progression via destabilizing IGF2BPs and activating anti-tumor immunity
title circNDUFB2 inhibits non-small cell lung cancer progression via destabilizing IGF2BPs and activating anti-tumor immunity
title_full circNDUFB2 inhibits non-small cell lung cancer progression via destabilizing IGF2BPs and activating anti-tumor immunity
title_fullStr circNDUFB2 inhibits non-small cell lung cancer progression via destabilizing IGF2BPs and activating anti-tumor immunity
title_full_unstemmed circNDUFB2 inhibits non-small cell lung cancer progression via destabilizing IGF2BPs and activating anti-tumor immunity
title_short circNDUFB2 inhibits non-small cell lung cancer progression via destabilizing IGF2BPs and activating anti-tumor immunity
title_sort circndufb2 inhibits non-small cell lung cancer progression via destabilizing igf2bps and activating anti-tumor immunity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7804955/
https://www.ncbi.nlm.nih.gov/pubmed/33436560
http://dx.doi.org/10.1038/s41467-020-20527-z
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