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

Author:

Dai Jia‐Zih12,Yang Ching‐Chieh34,Shueng Pei‐Wei56,Wang Yen‐Ju12,Huang Chen‐Shiuan2,Chao Yi‐Chun12,Chen Cheng‐Hsun2,Lin Cheng‐Wei1278ORCID

Affiliation:

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

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

3. Department of Radiation Oncology Chi Mei Medical Center Tainan Taiwan

4. Department of Pharmacy Chia‐Nan University of Pharmacy and Science Tainan Taiwan

5. Division of Radiation Oncology, Department of Radiology Far Eastern Memorial Hospital New Taipei City Taiwan

6. School of Medicine, College of Medicine National Yang Ming Chiao Tung University Taipei Taiwan

7. Cell Physiology and Molecular Image Research Center, Wan Fang Hospital Taipei Medical University Taipei Taiwan

8. Drug Development and Value Creation Research Center Kaohsiung Medical University Kaohsiung Taiwan

Abstract

AbstractObesity 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.

Funder

Ministry of Science and Technology, Taiwan

Chi Mei Medical Center

Publisher

Wiley

Subject

Cell Biology,Clinical Biochemistry,Physiology

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