Human ribonuclease 1 serves as a secretory ligand of ephrin A4 receptor and induces breast tumor initiation

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作者
Heng-Huan Lee
Ying-Nai Wang
Wen-Hao Yang
Weiya Xia
Yongkun Wei
Li-Chuan Chan
Yu-Han Wang
Zhou Jiang
Shouping Xu
Jun Yao
Yufan Qiu
Yi-Hsin Hsu
Wei-Lun Hwang
Meisi Yan
Jong-Ho Cha
Jennifer L. Hsu
Jia Shen
Yuanqing Ye
Xifeng Wu
Ming-Feng Hou
Lin-Ming Tseng
Shao-Chun Wang
Mei-Ren Pan
Chin-Hua Yang
Yuan-Liang Wang
Hirohito Yamaguchi
Da Pang
Gabriel N. Hortobagyi
Dihua Yu
Mien-Chie Hung
机构
[1] The University of Texas MD Anderson Cancer Center,Department of Molecular and Cellular Oncology
[2] China Medical University,Graduate Institute of Biomedical Sciences, Research Center for Cancer Biology, and Center for Molecular Medicine
[3] Harbin Medical University Cancer Hospital,Department of Breast Surgery
[4] Tianjin Medical University Cancer Institute and Hospital,Deptartment III of Breast Surgery
[5] National Yang Ming Chiao Tung University,Department of Biotechnology and Laboratory Science in Medicine
[6] National Yang-Ming University,Department of Biotechnology and Laboratory Science in Medicine
[7] Harbin Medical University,Department of Pathology
[8] College of Medicine,Department of Biomedical Sciences
[9] Inha University,Department of Epidemiology
[10] The University of Texas MD Anderson Cancer Center,Division of Breast Surgery, Department of Surgery
[11] Kaohsiung Medical University Hospital,Graduate Institute of Clinical Medicine
[12] Kaohsiung Medical University,Comprehensive Breast Health Center and Division of General Surgery, Department of Surgery
[13] Taipei Veterans General Hospital,Institute of Clinical Medicine and Faculty of Medicine, School of Medicine
[14] National Yang-Ming University,Department of Breast Medical Oncology
[15] The University of Texas MD Anderson Cancer Center,Department of Biotechnology
[16] Asia University,undefined
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摘要
Human ribonuclease 1 (hRNase 1) is critical to extracellular RNA clearance and innate immunity to achieve homeostasis and host defense; however, whether it plays a role in cancer remains elusive. Here, we demonstrate that hRNase 1, independently of its ribonucleolytic activity, enriches the stem-like cell population and enhances the tumor-initiating ability of breast cancer cells. Specifically, secretory hRNase 1 binds to and activates the tyrosine kinase receptor ephrin A4 (EphA4) signaling to promote breast tumor initiation in an autocrine/paracrine manner, which is distinct from the classical EphA4-ephrin juxtacrine signaling through contact-dependent cell-cell communication. In addition, analysis of human breast tumor tissue microarrays reveals a positive correlation between hRNase 1, EphA4 activation, and stem cell marker CD133. Notably, high hRNase 1 level in plasma samples is positively associated with EphA4 activation in tumor tissues from breast cancer patients, highlighting the pathological relevance of the hRNase 1-EphA4 axis in breast cancer. The discovery of hRNase 1 as a secretory ligand of EphA4 that enhances breast cancer stemness suggests a potential treatment strategy by inactivating the hRNase 1-EphA4 axis.
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