UBR5 通过 Lys 11 泛素依赖性稳定 Smad3-SLC7A11 信号,减弱铁凋亡,从而介导结直肠癌的化疗耐药性

IF 10.7 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Redox Biology Pub Date : 2024-09-10 DOI:10.1016/j.redox.2024.103349
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引用次数: 0

摘要

化疗耐药性仍然是结直肠癌(CRC)治疗失败的罪魁祸首,尤其是对复发或转移性疾病患者而言。破译化疗耐药性的分子基础可能会为这种致命疾病带来新的治疗策略。在本文中,人类 CRC 中经常过度表达的 E3 泛素连接酶 UBR5 被证明主要通过抑制铁变态反应来介导化疗抗性。矛盾的是,UBR5 通过与 Lys 11 链接的多泛素化保护奥沙利铂激活的 Smad3 免于蛋白酶体依赖性降解。Smad3 的这种新型化学修饰有助于抑制 ATF3 的转录、诱导 SLC7A11 和抑制铁变态反应,从而导致化疗耐药性。因此,靶向 UBR5 与铁突变诱导剂联合使用可协同增效,使 CRC 对奥沙利铂诱导的细胞死亡敏感并控制肿瘤生长。这项研究首次揭示了 UBR5 在维持 TGFβ-Smad3 信号传导和调节铁突变过程中介导的 CRC 临床相关的主要化疗耐药机制,揭示了其作为化疗增敏的可行治疗靶点的潜力。
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UBR5 mediates colorectal cancer chemoresistance by attenuating ferroptosis via Lys 11 ubiquitin-dependent stabilization of Smad3-SLC7A11 signaling

Chemoresistance remains a principal culprit for the treatment failure in colorectal cancer (CRC), especially for patients with recurrent or metastatic disease. Deciphering the molecular basis of chemoresistance may lead to novel therapeutic strategies for this fatal disease. Here, UBR5, an E3 ubiquitin ligase frequently overexpressed in human CRC, is demonstrated to mediate chemoresistance principally by inhibiting ferroptosis. Paradoxically, UBR5 shields oxaliplatin-activated Smad3 from proteasome-dependent degradation via Lys 11-linked polyubiquitination. This novel chemical modification of Smad3 facilitates the transcriptional repression of ATF3, induction of SLC7A11 and inhibition of ferroptosis, contributing to chemoresistance. Consequently, targeting UBR5 in combination with a ferroptosis inducer synergistically sensitizes CRC to oxaliplatin-induced cell death and control of tumor growth. This study reveals, for the first time, a major clinically relevant chemoresistance mechanism in CRC mediated by UBR5 in sustaining TGFβ-Smad3 signaling and tuning ferroptosis, unveiling its potential as a viable therapeutic target for chemosensitization.

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来源期刊
Redox Biology
Redox Biology BIOCHEMISTRY & MOLECULAR BIOLOGY-
CiteScore
19.90
自引率
3.50%
发文量
318
审稿时长
25 days
期刊介绍: Redox Biology is the official journal of the Society for Redox Biology and Medicine and the Society for Free Radical Research-Europe. It is also affiliated with the International Society for Free Radical Research (SFRRI). This journal serves as a platform for publishing pioneering research, innovative methods, and comprehensive review articles in the field of redox biology, encompassing both health and disease. Redox Biology welcomes various forms of contributions, including research articles (short or full communications), methods, mini-reviews, and commentaries. Through its diverse range of published content, Redox Biology aims to foster advancements and insights in the understanding of redox biology and its implications.
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