Activation of ERβ hijacks the splicing machinery to trigger R- loop formation in triple- negative breast cancer

• 成果类型: Article
• 署名作者: Wang, Dongfang; Tang, Muya; Zhang, Peidong; Yang, Kailin; Huang, Liang; Wu, Mengrui; Shen, Qiuhong; Yue, Jing; Wang, Wei; Gong, Yanqiu; Warner, Margaret; Dai, Lunzhi; He, Haihuai; Yang, Zhengnan; Gustafsson, Jan-Ake; Zhou, Shengtao
• 署名单位: Sichuan University; Sichuan University; Cleveland Clinic Foundation; Sichuan University; Sichuan University; University of Houston System; University of Houston; Sichuan University; Karolinska Institutet
• 刊物名称: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
• ISSN/ISSBN: 0027-14212
• DOI: 10.1073/pnas.2306814121
• 发表日期: 2024-03-26
• 关键词: transcriptional pause sites; dna-damage; rna; glutamate; RECOGNITION; mutations; mechanism; reveals; PATHWAY; GROWTH

摘要

Triple- negative breast cancer (TNBC) is a subtype of breast cancer with aggressive behavior and poor prognosis. Current therapeutic options available for TNBC patients are primarily chemotherapy. With our evolving understanding of this disease, novel targeted therapies, including poly ADP- ribose polymerase (PARP) inhibitors, antibody-drug conjugates, and immune- checkpoint inhibitors, have been developed for clinical use. Previous reports have demonstrated the essential role of estrogen receptor beta (ER beta) in TNBC, but the detailed molecular mechanisms downstream ER beta activation in TNBC are still far from elucidated. In this study, we demonstrated that a specific ER beta agonist, LY500307, potently induces R-loop formation and DNA damage in TNBC cells. Subsequent interactome experiments indicated that the residues 151 to 165 of U2 small nuclear RNA auxiliary factor 1 (U2AF1) and the Trp439 and Lys443 of ER beta were critical for the binding between U2AF1 and ER beta. Combined RNA sequencing and ribosome sequencing analysis demonstrated that U2AF1- regulated downstream RNA splicing of 5- oxoprolinase (OBLAH) could affect its enzymatic activity and is essential for ER beta- induced R-loop formation and DNA damage. In clinical samples including 115 patients from The Cancer Genome Atlas (TCGA) and 32 patients from an in-house cohort, we found a close correlation in the expression ofESR2 and U2AF1 in TNBC patients. Collectively, our study has unraveled the molecular mechanisms that explain the therapeutic effects of ER beta activation in TNBC, which provides rationale for ER beta activation-based single or combined therapy for patients with TNBC.