The basics of epithelial-mesenchymal transition

被引:8576
作者
Kalluri, Raghu [1 ,2 ,3 ]
Weinberg, Robert A. [4 ,5 ]
机构
[1] Harvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Div Matrix Biol, Boston, MA 02215 USA
[2] Harvard Univ, Sch Med, Dept Biol Chem & Mol Pharmacol, Boston, MA 02115 USA
[3] Harvard Mit Div Hlth Sci & Technol, Boston, MA USA
[4] MIT, Whitehead Inst Biomed Res, Ludwig Ctr Mol Oncol, Cambridge, MA USA
[5] MIT, Dept Biol, Cambridge, MA USA
关键词
GROWTH-FACTOR-BETA; RENAL INTERSTITIAL FIBROSIS; PRIMITIVE STREAK FORMATION; TGF-BETA; E-CADHERIN; NEURAL CREST; TUMOR-METASTASIS; SMAD PROTEINS; CHICK-EMBRYO; TRANSCRIPTION FACTOR;
D O I
10.1172/JCI39104
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
The origins of the mesenchymal cells participating in tissue repair and pathological processes, notably tissue fibrosis, tumor invasiveness, and metastasis, are poorly understood. However, emerging evidence suggests that epithelial-mesenchymal transitions (EMTs) represent one important source of these cells. As we discuss here, processes similar to the EMTs associated with embryo implantation, embryogenesis, and organ development are appropriated and subverted by chronically inflamed tissues and neoplasias. The identification of the signaling pathways that lead to activation of EMT programs during these disease processes is providing new insights into the plasticity of cellular phenotypes and possible therapeutic interventions.
引用
收藏
页码:1420 / 1428
页数:9
相关论文
共 129 条
[1]   Epithelial-mesenchymal transitions: the importance of changing cell state in development and disease [J].
Acloque, Herve ;
Adams, Meghan S. ;
Fishwick, Katherine ;
Bronner-Fraser, Marianne ;
Angela Nieto, M. .
JOURNAL OF CLINICAL INVESTIGATION, 2009, 119 (06) :1438-1449
[2]   Induction of EMT by twist proteins as a collateral effect of tumor-promoting inactivation of premature senescence [J].
Ansieau, Stephane ;
Bastid, Jeremy ;
Doreau, Agnes ;
Morel, Anne-Pierre ;
Bouchet, Benjamin P. ;
Thomas, Clemence ;
Fauvet, Frederique ;
Puisieux, Isabelle ;
Doglioni, Claudio ;
Piccinin, Sara ;
Maestro, Roberta ;
Voeltzel, Thibault ;
Selmi, Abdelkader ;
Valsesia-Wittmann, Sandrine ;
de Fromentel, Claude Caron ;
Puisieux, Alain .
CANCER CELL, 2008, 14 (01) :79-89
[3]  
Aplin John D., 1998, Hum Fertil (Camb), V1, P75, DOI 10.1080/1464727982000198161
[4]   Pivotal roles for eomesodermin during axis formation, epithelium-to-mesenchyme transition and endoderm specification in the mouse [J].
Arnold, Sebastian J. ;
Hofmann, Ulf K. ;
Bikoff, Elizabeth K. ;
Robertson, Elizabeth J. .
DEVELOPMENT, 2008, 135 (03) :501-511
[5]   EPITHELIAL MESENCHYMAL INTERACTIONS IN THE DEVELOPING KIDNEY LEAD TO EXPRESSION OF TENASCIN IN THE MESENCHYME [J].
AUFDERHEIDE, E ;
CHIQUETEHRISMANN, R ;
EKBLOM, P .
JOURNAL OF CELL BIOLOGY, 1987, 105 (01) :599-608
[6]   Evidence for a Role of Epithelial Mesenchymal Transition During Pathogenesis of Fistulae in Crohn's Disease [J].
Bataille, Frauke ;
Rohrmeier, Christian ;
Bates, Richard ;
Weber, Achim ;
Rieder, Florian ;
Brenmoehl, Julia ;
Strauch, Ulrike ;
Farkas, Stefan ;
Fuerst, Alois ;
Hofstaedter, Ferdinand ;
Schoelmerich, Juergen ;
Herfarth, Hans ;
Rogler, Gerhard .
INFLAMMATORY BOWEL DISEASES, 2008, 14 (11) :1514-1527
[7]   Integrin β1 signaling is necessary for transforming growth factor-β activation of p38MAPK and epithelial plasticity [J].
Bhowmick, NA ;
Zent, R ;
Ghiassi, M ;
McDonnell, M ;
Moses, HL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (50) :46707-46713
[8]   Transforming growth factor-β1 mediates epithelial to mesenchymal transdifferentiation through a RhoA-dependent mechanism [J].
Bhowmick, NA ;
Ghiassi, M ;
Bakin, A ;
Aakre, M ;
Lundquist, CA ;
Engel, ME ;
Arteaga, CL ;
Moses, HL .
MOLECULAR BIOLOGY OF THE CELL, 2001, 12 (01) :27-36
[9]   TGFβ:: the molecular Jekyll and Hyde of cancer [J].
Bierie, Brian ;
Moses, Harold L. .
NATURE REVIEWS CANCER, 2006, 6 (07) :506-520
[10]  
BIRCHMEIER W, 1994, BIOCHIM BIOPHYS ACTA, V1198, P1