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This process is characterized by decreased epithelial phenotypes\/markers and increased mesenchymal phenotypes\/markers. Tubular epithelial cells (TECs) are commonly susceptible to EMT by various stimuli, for example, transforming growth factor\u2010\u03b2 (TGF\u2010\u03b2), cellular communication network factor 2, angiotensin\u2010II, fibroblast growth factor\u20102, oncostatin M, matrix metalloproteinase\u20102, tissue plasminogen activator (t\u2010PA), plasmin, interleukin\u20101\u03b2, and reactive oxygen species. Similarly, glomerular podocytes can undergo EMT via these stimuli and by high glucose condition in diabetic kidney disease. EMT of TECs and podocytes leads to tubulointerstitial fibrosis and glomerulosclerosis, respectively. Signaling pathways involved in EMT\u2010mediated kidney fibrosis are diverse and complex. TGF\u2010\u03b21\/Smad and Wnt\/\u03b2\u2010catenin pathways are the major venues triggering EMT in TECs and podocytes. These two pathways thus serve as the major therapeutic targets against EMT\u2010mediated kidney fibrosis. To date, a number of EMT inhibitors have been identified and characterized. As expected, the majority of these EMT inhibitors affect TGF\u2010\u03b21\/Smad and Wnt\/\u03b2\u2010catenin pathways. In addition to kidney fibrosis, these EMT\u2010targeted antifibrotic inhibitors are expected to be effective for treatment against fibrosis in other organs\/tissues.<\/jats:p>","DOI":"10.1002\/dvg.23529","type":"journal-article","created":{"date-parts":[[2023,6,24]],"date-time":"2023-06-24T14:52:15Z","timestamp":1687618335000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":67,"title":["Epithelial\u2013mesenchymal plasticity in kidney fibrosis"],"prefix":"10.1002","volume":"62","author":[{"given":"Sudarat","family":"Hadpech","sequence":"first","affiliation":[{"name":"Medical Proteomics Unit, Research Department, Faculty of Medicine Siriraj Hospital Mahidol University  Bangkok Thailand"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-7865-0765","authenticated-orcid":false,"given":"Visith","family":"Thongboonkerd","sequence":"additional","affiliation":[{"name":"Medical Proteomics 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