Suppr超能文献

E3泛素连接酶RNF128通过触发白细胞介素-6受体的降解来减轻结肠炎和结直肠癌的发生。

E3 ubiquitin ligase RNF128 attenuates colitis and colorectal tumorigenesis by triggering the degradation of IL-6 receptors.

作者信息

He Tian-Sheng, Cai Kuntai, Lai Weiling, Yu Jingge, Qing Furong, Shen Ao, Sui Lina, He Wenji, Wang Weihua, Xiao Qiuxiang, Lei Xiong, Guo Tianfu, Liu Zhiping

机构信息

Center for Immunology, Key Laboratory of Prevention and Treatment of Cardiovascular and Cerebrovascular Diseases, Ministry of Education, Gannan Medical University, Ganzhou, Jiangxi, China; School of Basic Medicine, Gannan Medical University, Ganzhou, Jiangxi, China.

Center for Immunology, Key Laboratory of Prevention and Treatment of Cardiovascular and Cerebrovascular Diseases, Ministry of Education, Gannan Medical University, Ganzhou, Jiangxi, China; Graduate School, Gannan Medical University, Ganzhou, Jiangxi, China.

出版信息

J Adv Res. 2025 Jun;72:107-120. doi: 10.1016/j.jare.2024.06.025. Epub 2024 Jul 2.

Abstract

INTRODUCTION

Intestinal immune dysregulation is strongly linked to the occurrence and formation of tumors. RING finger protein 128 (RNF128) has been identified to play distinct immunoregulatory functions in innate and adaptive systems. However, the physiological roles of RNF128 in intestinal inflammatory conditions such as colitis and colorectal cancer (CRC) remain controversial.

OBJECTIVES

To elucidate the function and mechanism of RNF128 in colitis and CRC.

METHODS

Animal models of dextran sodium sulfate (DSS)-induced colitis and azoxymethane (AOM)/DSS-induced CRC were established in WT and Rnf128-deficient mice and evaluated by histopathology. Co-immunoprecipitation and ubiquitination analyses were employed to investigate the role of RNF128 in IL-6-STAT3 signaling.

RESULTS

RNF128 was significantly downregulated in clinical CRC tissues compared with paired peritumoral tissues. Rnf128-deficient mice were hypersusceptible to both colitis induced by DSS and CRC induced by AOM/DSS or APC mutation. Loss of RNF128 promoted the proliferation of CRC cells and STAT3 activation during the early transformative stage of carcinogenesis in vivo and in vitro when stimulated by IL-6. Mechanistically, RNF128 interacted with the IL-6 receptor α subunit (IL-6Rα) and membrane glycoprotein gp130 and mediated their lysosomal degradation in ligase activity-dependent manner. Through a series of point mutations in the IL-6 receptor, we identified that RNF128 promoted K48-linked polyubiquitination of IL-6Rα at K398/K401 and gp130 at K718/K816/K866. Additionally, blocking STAT3 activation effectively eradicated the inflammatory damage of Rnf128-deficient mice during the transformative stage of carcinogenesis.

CONCLUSION

RNF128 attenuates colitis and colorectal tumorigenesis by inhibiting IL-6-STAT3 signaling, which sheds novel insights into the modulation of IL-6 receptors and the inflammation-to-cancer transition.

摘要

引言

肠道免疫失调与肿瘤的发生和形成密切相关。已证实环指蛋白128(RNF128)在先天性和适应性免疫系统中发挥独特的免疫调节功能。然而,RNF128在诸如结肠炎和结直肠癌(CRC)等肠道炎症性疾病中的生理作用仍存在争议。

目的

阐明RNF128在结肠炎和结直肠癌中的功能及机制。

方法

在野生型和Rnf128基因缺陷型小鼠中建立葡聚糖硫酸钠(DSS)诱导的结肠炎和氧化偶氮甲烷(AOM)/DSS诱导的结直肠癌动物模型,并通过组织病理学进行评估。采用免疫共沉淀和泛素化分析来研究RNF128在IL-6-STAT3信号通路中的作用。

结果

与配对的肿瘤旁组织相比,临床结直肠癌组织中RNF128显著下调。Rnf128基因缺陷型小鼠对DSS诱导的结肠炎以及AOM/DSS或APC突变诱导的结直肠癌均高度敏感。在体内和体外,当受到IL-6刺激时,RNF128的缺失在致癌作用的早期转化阶段促进了结直肠癌细胞的增殖和STAT3激活。机制上,RNF128与IL-6受体α亚基(IL-6Rα)和膜糖蛋白gp130相互作用,并以连接酶活性依赖的方式介导它们的溶酶体降解。通过对IL-6受体进行一系列点突变,我们发现RNF128促进了IL-6Rα在K398/K401位点以及gp130在K718/K816/K866位点的K48连接的多聚泛素化。此外,阻断STAT3激活有效地消除了Rnf128基因缺陷型小鼠在致癌转化阶段的炎症损伤。

结论

RNF128通过抑制IL-6-STAT3信号通路减轻结肠炎和结直肠癌的发生,这为IL-6受体的调节以及炎症向癌症的转变提供了新的见解。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验