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c-Myc-activated USP2-AS1 suppresses senescence and promotes tumor progression via stabilization of E2F1 mRNA

Bingyan Li, Guang Zhang, Zhongyu Wang, Yang Yang, Chenfeng Wang, Debao Fang, Kaiyue Liu, Fang Wang, Yide Mei

2021Cell Death and Disease28 citationsDOIOpen Access PDF

Abstract

The c-Myc oncoprotein plays a prominent role in cancer initiation, progression, and maintenance. Long noncoding RNAs (lncRNAs) are recently emerging as critical regulators of the c-Myc signaling pathway. Here, we report the lncRNA USP2-AS1 as a direct transcriptional target of c-Myc. Functionally, USP2-AS1 inhibits cellular senescence and acts as an oncogenic molecule by inducing E2F1 expression. Mechanistically, USP2-AS1 associates with the RNA-binding protein G3BP1 and facilitates the interaction of G3BP1 to E2F1 3'-untranslated region, thereby leading to the stabilization of E2F1 messenger RNA. Furthermore, USP2-AS1 is shown as a mediator of the oncogenic function of c-Myc via the regulation of E2F1. Together, these findings suggest that USP2-AS1 is a negative regulator of cellular senescence and also implicates USP2-AS1 as an important player in mediating c-Myc function.

Topics & Concepts

SenescenceCancer researchChemistryMessenger RNACell biologyBiologyBiochemistryGeneRNA modifications and cancerCancer-related molecular mechanisms researchRNA Research and Splicing