The feedback loop between miR-222-3p and ZEB1 harnesses metastasis in renal cell carcinoma

被引:0
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作者
Fan Wang [1 ]
Liao Li [2 ]
Xiangfu Sun [3 ]
Xianfu Cai [4 ]
Jianjun Wang [5 ]
Huiwen Luo [6 ]
Yaodong Wang [7 ]
Dong Ni [8 ]
Decai Wang [7 ]
机构
[1] Hubei University of Medicine,Department of Thyroid and Breast Surgery, Xiangyang No. 1 People’s Hospital
[2] Hubei University of Medicine,Department of Child Healthcare, Xiangyang No. 1 People’s Hospital
[3] Hubei University of Medicine,Department of Cardiothoracic Surgery, Xiangyang No. 1 People’s Hospital
[4] the First Affiliated Hospital of Xi’an Jiaotong University,Department of Renal Transplantation
[5] University of Electronic Science and Technology of China,Department of Hepatobiliary Surgery, Mianyang Central Hospital, School of Medicine
[6] University of Electronic Science and Technology of China,NHC Key Laboratory of Nuclear Technology Medical Transformation, Mianyang Central Hospital, School of Medicine
[7] University of Electronic Science and Technology of China,Department of Urology, Mianyang Central Hospital, School of Medicine
[8] Huazhong University of Science and Technology,Department of Urology, Union Hospital, Tongji Medical College
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10.1038/s41420-025-02385-0
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摘要
Renal cell carcinoma (RCC) is an aggressive malignancy originating from the renal parenchyma, often leading to high mortality due to local invasion and distant metastasis. MicroRNAs (miRNAs) play essential roles in RCC progression. Through miRNA sequencing, we identified significant upregulation of miR-222-3p in metastatic RCC tissues. Exosomes from highly metastatic RCC cells were found to transfer miR-222-3p to low-metastatic cells, enhancing their migration and invasion. Mechanistically, miR-222-3p directly targets the 3′ untranslated region (3′UTR) of the tumor-suppressor TRPS1, reducing its expression. TRPS1 downregulation releases its inhibitory effect on ZEB1, a key regulator of epithelial-mesenchymal transition (EMT), thereby promoting EMT and metastatic traits. ZEB1 further transactivates miR-222-3p, establishing a positive feedback loop. Additionally, miR-222-3p promotes a pre-metastatic niche by inducing M2 macrophage polarization, facilitating distant metastasis. These findings highlight miR-222-3p as a critical driver of RCC metastasis and suggest its potential as a diagnostic marker and therapeutic target for RCC.
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