Biomarkers for epithelial-mesenchymal transitions

被引:2048
作者
Zeisberg, Michael [3 ]
Neilson, Eric G. [1 ,2 ]
机构
[1] Vanderbilt Univ, Sch Med, Dept Med, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Sch Med, Dept Cell & Dev Biol, Nashville, TN 37232 USA
[3] Harvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Div Matrix Biol, Boston, MA USA
关键词
INTERMEDIATE-SIZED FILAMENTS; BREAST-CANCER; RENAL FIBROSIS; CELL INVASION; BETA-CATENIN; STEM-CELLS; INTERSTITIAL FIBROGENESIS; TRANSCRIPTION FACTORS; EXTRACELLULAR-MATRIX; CONFERS RESISTANCE;
D O I
10.1172/JCI36183
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Somatic cells that change from one mature phenotype to another exhibit the property of plasticity. It is increasingly clear that epithelial and endothelial cells enjoy some of this plasticity, which is easily demonstrated by studying the process of epithelial-mesenchymal transition (EMT). Published reports from the literature typically rely on ad hoc criteria for determining EMT events; consequently, there is some uncertainty as to whether the same process occurs under different experimental conditions. As we discuss in this Personal Perspective, we believe that context and various changes in plasticity biomarkers can help identify at least three types of EMT and that using a collection of criteria for EMT increases the likelihood that everyone is studying the same phenomenon - namely, the transition of epithelial and endothelial cells to a motile phenotype.
引用
收藏
页码:1429 / 1437
页数:9
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