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枫脂酸通过靶向 TNF 受体相关因子 2 抑制 Wnt/β-catenin 信号通路和结肠癌。

Liquidambaric acid inhibits Wnt/β-catenin signaling and colon cancer via targeting TNF receptor-associated factor 2.

机构信息

Center for Chemical Biology, Institute of Interdisciplinary Integrative Medicine Research, Shanghai University of Traditional Chinese Medicine, No.1200 Cailun Road, Shanghai 201203, P.R. China; Shanghai Frontiers Science Center of TCM Chemical Biology, Institute of Interdisciplinary Integrative Medicine Research, Shanghai University of Traditional Chinese Medicine, No.1200 Cailun Road, Shanghai 201203, China.

School of Life Science and Technology, ShanghaiTech University, 393 Middle Huaxia Road, Shanghai 201210, P.R. China.

出版信息

Cell Rep. 2022 Feb 1;38(5):110319. doi: 10.1016/j.celrep.2022.110319.

Abstract

Wnt/β-catenin signaling is a well-established driver of colon cancer; however, a targeted therapeutic agent has not reached clinics yet. In the present study, we report that the natural compound liquidambaric acid (LDA) inhibits oncogenic Wnt/β-catenin signaling in vitro and in vivo through its direct target tumor necrosis factor receptor-associated factor 2 (TRAF2). Mechanistically, TRAF2 positively regulates Wnt signaling by interacting with the N-terminal of β-catenin via its TRAF-C domain; this interaction is disrupted in presence of LDA. Particularly, a TRAF2/β-catenin/TCF4/TNIK complex is present in colon cancer cells, where TRAF2 is indispensable for the complex formation, and TRAF2/β-catenin and β-catenin/TCF4 interactions are disrupted upon LDA treatment. Our findings not only highlight that TRAF2 is an oncogenic regulator of Wnt/β-catenin signaling and colon cancer but also provide a lead compound targeting TRAF2 for cancer therapy.

摘要

Wnt/β-catenin 信号通路是结直肠癌的一个既定驱动因素;然而,一种靶向治疗药物尚未进入临床应用。在本研究中,我们报告称,天然化合物液体阿拉伯酸(LDA)通过其直接靶标肿瘤坏死因子受体相关因子 2(TRAF2)在体外和体内抑制致癌的 Wnt/β-catenin 信号通路。从机制上讲,TRAF2 通过其 TRAF-C 结构域与 β-catenin 的 N 端相互作用,正向调节 Wnt 信号;这种相互作用在 LDA 的存在下被破坏。特别是,在结肠癌细胞中存在 TRAF2/β-catenin/TCF4/TNIK 复合物,其中 TRAF2 对于复合物的形成是必不可少的,并且 TRAF2/β-catenin 和 β-catenin/TCF4 相互作用在 LDA 处理后被破坏。我们的研究结果不仅强调了 TRAF2 是 Wnt/β-catenin 信号通路和结直肠癌的致癌调节剂,而且还提供了一种针对 TRAF2 的先导化合物,用于癌症治疗。

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