Wen-Yu Chuang , Chao-Wei Lee , Wen-Lang Fan , Tsung-Ta Liu , Zih-Han Lin , Kuo-Chih Wang , Po-Jung Huang , Yuan-Ming Yeh , Tsung-Chieh Lin
{"title":"Wnt-5a-ROR2信号在肾细胞癌中引发转移性定植和血管生成,梅花素抑制了该轴的激活。","authors":"Wen-Yu Chuang , Chao-Wei Lee , Wen-Lang Fan , Tsung-Ta Liu , Zih-Han Lin , Kuo-Chih Wang , Po-Jung Huang , Yuan-Ming Yeh , Tsung-Chieh Lin","doi":"10.1016/j.ajpath.2024.07.003","DOIUrl":null,"url":null,"abstract":"<div><div>Wnt-5a is a protein encoded by the <em>WNT5A</em> gene and is a ligand for the receptor tyrosine kinase-like orphan receptor 2 (ROR2). However, its biological impact on clear cell renal cell carcinoma (ccRCC) remains unclear. In this study, the prognostic significance of concurrent <em>WNT5A</em> and <em>ROR2</em> expression levels was observed to predict unfavorable overall survival and disease-specific survival. High Wnt-5a expression was detected in a ccRCC cell line panel but not in HK-2 cells, a normal proximal tubular cell line. Inhibition of DNA methyltransferase by 5-azacytidine in 786-O and Caki-2 cells resulted in Wnt-5a up-regulation, indicating potential epigenetic modification. Furthermore, there was a repression of cell movement <em>in vitro</em> and metastatic colonization <em>in vivo</em> on <em>WNT5A</em> and <em>ROR2</em> knockdown. Suppressions of angiogenesis <em>in vivo</em> and tubular-like structure formation in endothelial cells <em>in vitro</em> were also observed after silencing <em>WNT5A</em> and <em>ROR2</em> expression. In addition, alteration in the downstream gene signature of the Wnt-5a–ROR2 signaling was similar to that in metastasis-associated gene 1–β-catenin axis. Moreover, prunetin treatment reversed the gene signature derived from Wnt-5a–ROR2 signaling activation and to abolish ccRCC cell migration and proliferation. Overall, this study demonstrates the clinical and functional significance of the Wnt-5a–ROR2 axis and identifies prunetin as a potential precision medicine for patients with ccRCC harboring aberrant Wnt-5a–ROR2 signaling pathways.</div></div>","PeriodicalId":7623,"journal":{"name":"American Journal of Pathology","volume":"194 10","pages":"Pages 1967-1985"},"PeriodicalIF":4.7000,"publicationDate":"2024-07-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Wnt-5a–Receptor Tyrosine Kinase-Like Orphan Receptor 2 Signaling Provokes Metastatic Colonization and Angiogenesis in Renal Cell Carcinoma, and Prunetin Supresses the Axis Activation\",\"authors\":\"Wen-Yu Chuang , Chao-Wei Lee , Wen-Lang Fan , Tsung-Ta Liu , Zih-Han Lin , Kuo-Chih Wang , Po-Jung Huang , Yuan-Ming Yeh , Tsung-Chieh Lin\",\"doi\":\"10.1016/j.ajpath.2024.07.003\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Wnt-5a is a protein encoded by the <em>WNT5A</em> gene and is a ligand for the receptor tyrosine kinase-like orphan receptor 2 (ROR2). However, its biological impact on clear cell renal cell carcinoma (ccRCC) remains unclear. In this study, the prognostic significance of concurrent <em>WNT5A</em> and <em>ROR2</em> expression levels was observed to predict unfavorable overall survival and disease-specific survival. High Wnt-5a expression was detected in a ccRCC cell line panel but not in HK-2 cells, a normal proximal tubular cell line. Inhibition of DNA methyltransferase by 5-azacytidine in 786-O and Caki-2 cells resulted in Wnt-5a up-regulation, indicating potential epigenetic modification. Furthermore, there was a repression of cell movement <em>in vitro</em> and metastatic colonization <em>in vivo</em> on <em>WNT5A</em> and <em>ROR2</em> knockdown. Suppressions of angiogenesis <em>in vivo</em> and tubular-like structure formation in endothelial cells <em>in vitro</em> were also observed after silencing <em>WNT5A</em> and <em>ROR2</em> expression. In addition, alteration in the downstream gene signature of the Wnt-5a–ROR2 signaling was similar to that in metastasis-associated gene 1–β-catenin axis. Moreover, prunetin treatment reversed the gene signature derived from Wnt-5a–ROR2 signaling activation and to abolish ccRCC cell migration and proliferation. Overall, this study demonstrates the clinical and functional significance of the Wnt-5a–ROR2 axis and identifies prunetin as a potential precision medicine for patients with ccRCC harboring aberrant Wnt-5a–ROR2 signaling pathways.</div></div>\",\"PeriodicalId\":7623,\"journal\":{\"name\":\"American Journal of Pathology\",\"volume\":\"194 10\",\"pages\":\"Pages 1967-1985\"},\"PeriodicalIF\":4.7000,\"publicationDate\":\"2024-07-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"American Journal of Pathology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0002944024002451\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PATHOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"American Journal of Pathology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0002944024002451","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PATHOLOGY","Score":null,"Total":0}
Wnt-5a–Receptor Tyrosine Kinase-Like Orphan Receptor 2 Signaling Provokes Metastatic Colonization and Angiogenesis in Renal Cell Carcinoma, and Prunetin Supresses the Axis Activation
Wnt-5a is a protein encoded by the WNT5A gene and is a ligand for the receptor tyrosine kinase-like orphan receptor 2 (ROR2). However, its biological impact on clear cell renal cell carcinoma (ccRCC) remains unclear. In this study, the prognostic significance of concurrent WNT5A and ROR2 expression levels was observed to predict unfavorable overall survival and disease-specific survival. High Wnt-5a expression was detected in a ccRCC cell line panel but not in HK-2 cells, a normal proximal tubular cell line. Inhibition of DNA methyltransferase by 5-azacytidine in 786-O and Caki-2 cells resulted in Wnt-5a up-regulation, indicating potential epigenetic modification. Furthermore, there was a repression of cell movement in vitro and metastatic colonization in vivo on WNT5A and ROR2 knockdown. Suppressions of angiogenesis in vivo and tubular-like structure formation in endothelial cells in vitro were also observed after silencing WNT5A and ROR2 expression. In addition, alteration in the downstream gene signature of the Wnt-5a–ROR2 signaling was similar to that in metastasis-associated gene 1–β-catenin axis. Moreover, prunetin treatment reversed the gene signature derived from Wnt-5a–ROR2 signaling activation and to abolish ccRCC cell migration and proliferation. Overall, this study demonstrates the clinical and functional significance of the Wnt-5a–ROR2 axis and identifies prunetin as a potential precision medicine for patients with ccRCC harboring aberrant Wnt-5a–ROR2 signaling pathways.
期刊介绍:
The American Journal of Pathology, official journal of the American Society for Investigative Pathology, published by Elsevier, Inc., seeks high-quality original research reports, reviews, and commentaries related to the molecular and cellular basis of disease. The editors will consider basic, translational, and clinical investigations that directly address mechanisms of pathogenesis or provide a foundation for future mechanistic inquiries. Examples of such foundational investigations include data mining, identification of biomarkers, molecular pathology, and discovery research. Foundational studies that incorporate deep learning and artificial intelligence are also welcome. High priority is given to studies of human disease and relevant experimental models using molecular, cellular, and organismal approaches.