研究动态
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NUAK1 激活 STAT5/GLI1/SOX2 信号传导以增强癌细胞增殖并驱动胃癌的化疗耐药性。

NUAK1 activates STAT5/GLI1/SOX2 signaling to enhance cancer cell expansion and drives chemoresistance in gastric cancer.

发表日期:2024 Jul 10
作者: Longlong Cao, Guangtan Lin, Denghui Fan, Kai Weng, Yujing Chen, Jiabin Wang, Ping Li, Chaohui Zheng, Changming Huang, Jianwei Xie
来源: Cell Reports

摘要:

编码 NUAK 家族激酶 1 (NUAK1) 的基因经常被扩增,其表达上调,激活各种癌症中的致癌信号传导。然而,人们对其在胃癌(GC)中的作用知之甚少。我们研究了 NUAK1、Hedgehog 信号传导和 GC 肿瘤发生之间的机制联系。 NUAK1 过表达在本地和公共 GC 队列中得到验证。患者来源的异种移植和转基因小鼠模型表明,NUAK1 缺失或抑制可显着改善胃肿瘤的发生。 NUAK1 通过激活 STAT5 介导的转录并稳定 GLI1 蛋白来上调 GLI1 表达。 NUAK1 消耗或抑制会损害体外和体内模型中的癌细胞扩张、肿瘤形成和化疗耐药性。临床病理学分析证实,NUAK1 表达上调与人类 GC 的不良预后和化疗耐药相关。我们的研究结果表明,信号轴 NUAK1/STAT5/GLI1 促进癌细胞增殖和肿瘤发生,并表明 NUAK1 是 GC 中有吸引力的治疗靶点和预后因素。版权所有 © 2024。由 Elsevier Inc. 出版。
The gene encoding the NUAK family kinase 1 (NUAK1) is frequently amplified and its expression is upregulated, activating oncogenic signaling in various cancers. However, little is known about its role in gastric cancer (GC). We investigate the mechanistic links among NUAK1, Hedgehog signaling, and tumorigenesis in GC. NUAK1 overexpression is validated in local and public GC cohorts. Patient-derived xenograft and transgenic mouse models demonstrate that NUAK1 depletion or inhibition dramatically ameliorates gastric tumorigenesis. NUAK1 upregulates GLI1 expression by activating STAT5-mediated transcription and stabilizing GLI1 protein. NUAK1 depletion or inhibition impairs cancer cell expansion, tumor formation, and chemotherapy resistance in in vitro and in vivo models. Clinicopathological analysis confirms that upregulated NUAK1 expression correlates with poor prognosis and chemotherapy resistance in human GC. Our findings demonstrate that the signaling axis NUAK1/STAT5/GLI1 promotes cancer cell expansion and tumorigenesis and indicate that NUAK1 is an attractive therapeutic target and prognostic factor in GC.Copyright © 2024. Published by Elsevier Inc.