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肥胖介导的 YAP/IL33 信号轴的上调促进了乳腺癌的侵袭性,并诱导了免疫抑制性肿瘤微环境。

Obesity-mediated upregulation of the YAP/IL33 signaling axis promotes aggressiveness and induces an immunosuppressive tumor microenvironment in breast cancer.

机构信息

Graduate Institute of Medical Sciences, College of Medicine, Taipei Medical University, Taipei, Taiwan.

Department of Biochemistry and Molecular Cell Biology, Taipei Medical University, Taipei, Taiwan.

出版信息

J Cell Physiol. 2023 May;238(5):992-1005. doi: 10.1002/jcp.30985. Epub 2023 Feb 28.

DOI:10.1002/jcp.30985
PMID:36852589
Abstract

Obesity is a well-known risk factor for breast cancer formation and is associated with elevated mortality and a poor prognosis. An obesity-mediated inflammatory microenvironment is conducive to the malignant progression of tumors. However, the detailed molecular mechanism is still needed to be clarified. Herein, we identified that breast cancer cells from mice with diet-induced obesity exhibited increased growth, invasiveness, and stemness capacities. A transcriptome analysis revealed that expressions of interleukin 33 (IL33) signaling pathway-related genes were elevated in obesity-associated breast cancer cells. Importantly, IL33 expression was significantly associated with the yes-associated protein (YAP) signature, and IL33 was transcriptionally regulated by YAP. Suppression of IL33 reduced tumor migration and invasion, while the addition of IL33 activated nuclear factor (NF)-κB signaling and revived tumor mobility in YAP-silenced cells. Furthermore, suppression of YAP attenuated IL33 expression which was accompanied by relief of obesity-mediated immunosuppression. Clinical analyses showed that IL33 expression was markedly associated with macrophage and regulatory T cell infiltration. These findings reveal a crucial role of the YAP/IL33 axis in promoting aggressiveness and immunosuppression of obesity-associated breast cancer progression.

摘要

肥胖是乳腺癌形成的一个众所周知的危险因素,与死亡率升高和预后不良有关。肥胖介导的炎症微环境有利于肿瘤的恶性进展。然而,其详细的分子机制仍需要阐明。在此,我们发现饮食诱导肥胖的小鼠的乳腺癌细胞表现出生长、侵袭和干性能力的增加。转录组分析显示,白细胞介素 33(IL33)信号通路相关基因的表达在与肥胖相关的乳腺癌细胞中升高。重要的是,IL33 的表达与 yes 相关蛋白(YAP)特征显著相关,并且 IL33 受 YAP 转录调控。抑制 IL33 减少了肿瘤的迁移和侵袭,而在 YAP 沉默的细胞中添加 IL33 激活了核因子(NF)-κB 信号并恢复了肿瘤的迁移能力。此外,抑制 YAP 减弱了 IL33 的表达,伴随着肥胖介导的免疫抑制的缓解。临床分析表明,IL33 的表达与巨噬细胞和调节性 T 细胞浸润明显相关。这些发现揭示了 YAP/IL33 轴在促进肥胖相关乳腺癌进展的侵袭性和免疫抑制中的关键作用。

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引用本文的文献

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Exogenous IL-33 promotes tumor immunity via macroscopic regulation of ILC2s.外源性白介素 33 通过宏观调控 ILC2 促进肿瘤免疫。
Sci Rep. 2024 Oct 30;14(1):26140. doi: 10.1038/s41598-024-77751-6.
2
Decoding the IL-33/ST2 Axis: Its Impact on the Immune Landscape of Breast Cancer.解读白细胞介素-33/ST2轴:其对乳腺癌免疫格局的影响
Int J Mol Sci. 2023 Sep 13;24(18):14026. doi: 10.3390/ijms241814026.