Reassessing epithelial to mesenchymal transition as a prerequisite for carcinoma invasion and metastasis

被引:854
作者
Christiansen, Jason J.
Rajasekaran, Ayyappan K.
机构
[1] Univ Calif Los Angeles, Dept Pathol & Lab Med, David Geffen Sch Med, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Inst Mol Biol, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Jonsson Comprehens Canc Ctr, Los Angeles, CA 90024 USA
关键词
D O I
10.1158/0008-5472.CAN-06-0410
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
For most carcinomas, progression toward malignancy is accompanied by loss of epithelial differentiation and a shift towards a mesenchymal phenotype. This process, referred to as epithelial to mesenchymal transition (EMT), exacerbates motility and invasiveness of many cell types and is often considered a prerequisite for tumor infiltration and metastasis. However, there are numerous examples of advanced carcinomas that adopt some mesenchymal features, yet retain characteristics of well-differentiated epithelial cells. We provide a review of these reports and describe mechanisms to explain the morphologic and molecular heterogeneity and plasticity of malignant carcinoma cells, including incomplete EMT, reversion to an epithelial phenotype, and collective migration. We suggest that these mechanisms can manifest in a series of independent and reversible steps and that EMT represents just one mechanism in the global metastatic carcinoma development process.
引用
收藏
页码:8319 / 8326
页数:8
相关论文
共 94 条
[1]  
AHNEN DJ, 1982, CANCER, V49, P2077, DOI 10.1002/1097-0142(19820515)49:10<2077::AID-CNCR2820491020>3.0.CO
[2]  
2-X
[3]   Intravascular origin of metastasis from the proliferation of endothelium-attached tumor cells: a new model for metastasis [J].
Al-Mehdi, AB ;
Tozawa, K ;
Fisher, AB ;
Shientag, L ;
Lee, A ;
Muschel, RJ .
NATURE MEDICINE, 2000, 6 (01) :100-102
[4]   TIGHT JUNCTIONS AND THE MOLECULAR-BASIS FOR REGULATION OF PARACELLULAR PERMEABILITY [J].
ANDERSON, JM ;
VANITALLIE, CM .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1995, 269 (04) :G467-G475
[5]   The role of Rho GTPases in the regulation of the rearrangement of actin cytoskeleton and cell movement [J].
Begum, R ;
Nur-E-Kamal, MSA ;
Zaman, MA .
EXPERIMENTAL AND MOLECULAR MEDICINE, 2004, 36 (04) :358-366
[6]   DISSECTING TUMOR-CELL INVASION - EPITHELIAL-CELLS ACQUIRE INVASIVE PROPERTIES AFTER THE LOSS OF UVOMORULIN-MEDIATED CELL CELL-ADHESION [J].
BEHRENS, J ;
MAREEL, MM ;
VANROY, FM ;
BIRCHMEIER, W .
JOURNAL OF CELL BIOLOGY, 1989, 108 (06) :2435-2447
[7]   LOSS OF EPITHELIAL DIFFERENTIATION AND GAIN OF INVASIVENESS CORRELATES WITH TYROSINE PHOSPHORYLATION OF THE E-CADHERIN BETA-CATENIN COMPLEX IN CELLS TRANSFORMED WITH A TEMPERATURE-SENSITIVE V-SRC GENE [J].
BEHRENS, J ;
VAKAET, L ;
FRIIS, R ;
WINTERHAGER, E ;
VANROY, F ;
MAREEL, MM ;
BIRCHMEIER, W .
JOURNAL OF CELL BIOLOGY, 1993, 120 (03) :757-766
[8]   Src and Ras are involved in separate pathways in epithelial cell scattering [J].
Boyer, B ;
Roche, S ;
Denoyelle, M ;
Thiery, JP .
EMBO JOURNAL, 1997, 16 (19) :5904-5913
[9]   Induction by transforming growth factor-β1 of epithelial to mesenchymal transition is a rare event in vitro [J].
Brown, KA ;
Aakre, ME ;
Gorska, AE ;
Price, JO ;
Eltom, SE ;
Pietenpol, JA ;
Moses, HL .
BREAST CANCER RESEARCH, 2004, 6 (03) :R215-R231
[10]   RhoA, Rac1, and Cdc42 exert distinct effects on epithelial barrier via selective structural and biochemical modulation of junctional proteins and F-actin [J].
Bruewer, M ;
Hopkins, AM ;
Hobert, ME ;
Nusrat, A ;
Madara, JL .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2004, 287 (02) :C327-C335