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TRIB3 通过稳定 TAZ 赋予食管鳞癌细胞放射抵抗性。

TRIB3 confers radiotherapy resistance in esophageal squamous cell carcinoma by stabilizing TAZ.

机构信息

Department of Radiation Oncology, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangzhou, 510060, China.

Department of Experimental Research, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangzhou, 510060, China.

出版信息

Oncogene. 2020 Apr;39(18):3710-3725. doi: 10.1038/s41388-020-1245-0. Epub 2020 Mar 10.

Abstract

Radioresistance becomes the major obstacle to reduce tumor recurrence and improve prognosis in the treatment of esophageal squamous cell carcinoma (ESCC). Thus new strategies for radioresistant ESCC are urgently needed. Herein, we reported that tribbles pseudokinase 3 (TRIB3) serves as a key regulator of radioresistance in ESCC. TRIB3 is overexpressed in ESCC tissues and cell lines. High expression of TRIB3 significantly correlates with poor radiotherapy response and prognosis in ESCC patients. Upregulation of TRIB3 in ESCC cells conferred radioresistance in vitro and in vivo by interacting with TAZ thus impeding β-TrCP-mediated TAZ ubiquitination and degradation. Conversely, silencing TRIB3 sensitized ESCC cells to ionizing radiation. More importantly, TRIB3 was significantly correlated with TAZ activation in ESCC biopsies, and patients with high expression of both TRIB3 and TAZ suffered the worst radiotherapy response and survival. Our study uncovers the critical mechanism of ESCC resistance to radiotherapy, and provides a new pharmacological opportunity for developing a mechanism-based strategy to eliminate radioresistant ESCC in clinical practice.

摘要

放射抵抗成为降低食管癌(ESCC)肿瘤复发和改善预后的主要障碍。因此,迫切需要针对放射抵抗 ESCC 的新策略。在此,我们报道了 tribbles 假激酶 3(TRIB3)是 ESCC 放射抵抗的关键调节因子。TRIB3 在 ESCC 组织和细胞系中过表达。TRIB3 的高表达与 ESCC 患者放疗反应不良和预后不良显著相关。TRIB3 在 ESCC 细胞中的上调通过与 TAZ 相互作用赋予了体外和体内的放射抵抗作用,从而阻碍了 β-TrCP 介导的 TAZ 泛素化和降解。相反,沉默 TRIB3 可使 ESCC 细胞对电离辐射敏感。更重要的是,TRIB3 与 ESCC 活检中的 TAZ 激活显著相关,并且同时表达 TRIB3 和 TAZ 的患者放疗反应和生存最差。我们的研究揭示了 ESCC 对放疗抵抗的关键机制,并为开发基于机制的策略在临床实践中消除放射抵抗 ESCC 提供了新的药理学机会。

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