{"title":"TWIST1 regulation of circRNA: a novel mechanism to promote epithelial-mesenchymal transition in hepatocellular carcinoma.","authors":"Zachary A Yochum, Timothy F Burns","doi":"10.21037/ncri.2018.12.01","DOIUrl":null,"url":null,"abstract":"The epithelial-mesenchymal transition (EMT) is a process in which epithelial cells reversibly transdifferentiate and adopt a mesenchymal morphology (1-3). EMT is driven by suppression of epithelial associated genes such as E-cadherin and upregulation of mesenchymal associated genes such as fibroblast-specific protein 1 and Vimentin (1-3). These genetic changes lead epithelial cells to become more spindle-like in appearance due to loss of epithelial cell apical-basal polarity, cell-cell interactions, and cell-extracellular matrix interactions (1).","PeriodicalId":74314,"journal":{"name":"Non-coding RNA investigation","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2018-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.21037/ncri.2018.12.01","citationCount":"3","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Non-coding RNA investigation","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21037/ncri.2018.12.01","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2018/12/19 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 3
Abstract
The epithelial-mesenchymal transition (EMT) is a process in which epithelial cells reversibly transdifferentiate and adopt a mesenchymal morphology (1-3). EMT is driven by suppression of epithelial associated genes such as E-cadherin and upregulation of mesenchymal associated genes such as fibroblast-specific protein 1 and Vimentin (1-3). These genetic changes lead epithelial cells to become more spindle-like in appearance due to loss of epithelial cell apical-basal polarity, cell-cell interactions, and cell-extracellular matrix interactions (1).