Title：TRIB3 promotes MYC-associated lymphoma development through suppression of UBE3B-mediated MYC degradation

Author：Ke Li, Feng Wang, Zhao-Na Yang, Ting-Ting Zhang, Yu-Fen Yuan, Chen-Xi Zhao , Zaiwuli Yeerjiang , Bing Cui, Fang Hua, Xiao-Xi Lv, Xiao-Wei Zhang, Jiao-Jiao Yu, Shan-Shan Liu, Jin-Mei Yu, Shuang Shang, Yang Xiao, Zhuo-Wei Hu

Journal：Nat Commun

IF：12.121

Year：2020

Volume/Issue/Page：11(1):6316

The transcription factor MYC is deregulated in almost all human cancers, especially in aggressive lymphomas, through chromosomal translocation, amplification, and transcription hyperactivation. Here, we report that high expression of tribbles homologue 3 (TRIB3) positively correlates with elevated MYC expression in lymphoma specimens; TRIB3 deletion attenuates the initiation and progression of MYC-driven lymphoma by reducing MYC expression. Mechanistically, TRIB3 interacts with MYC to suppress E3 ubiquitin ligase UBE3B-mediated MYC ubiquitination and degradation, which enhances MYC transcriptional activity, causing high proliferation and self-renewal of lymphoma cells. Use of a peptide to disturb the TRIB3-MYC interaction together with doxorubicin reduces the tumor burden in MycEμ mice and patient-derived xenografts. The pathophysiological relevance of UBE3B, TRIB3 and MYC is further demonstrated in human lymphoma. Our study highlights a key mechanism for controlling MYC expression and a potential therapeutic option for treating lymphomas with high TRIB3-MYC expression.