Epithelial-Mesenchymal Transition: General Principles and Pathological Relevance with Special Emphasis on the Role of Matrix Metalloproteinases

被引:216
作者
Nistico, Paola [2 ]
Bissell, Mina J. [3 ]
Radisky, Derek C. [1 ]
机构
[1] Mayo Clin, Ctr Canc, Jacksonville, FL 32224 USA
[2] Regina Elena Inst Canc Res, Immunol Lab, I-00144 Rome, Italy
[3] Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Berkeley, CA 94720 USA
关键词
CANCER STEM-CELLS; MAMMARY BRANCHING MORPHOGENESIS; SARCOMA VIRUS TUMORIGENESIS; BENIGN BREAST DISEASE; TGF-BETA; E-CADHERIN; SPLICE VARIANT; PULMONARY-FIBROSIS; BASEMENT-MEMBRANE; CARCINOMA CELLS;
D O I
10.1101/cshperspect.a011908
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Epithelial-mesenchymal transition (EMT) is a physiological process in which epithelial cells acquire the motile and invasive characteristics of mesenchymal cells. Although EMT in embryonic development is a coordinated, organized process involving interaction between many different cells and tissue types, aspects of the EMT program can be inappropriately activated in response to microenvironmental alterations and aberrant stimuli, and this can contribute to disease conditions including tissue fibrosis and cancer progression. Here we will outline how EMT functions in normal development, how it could be activated in pathologic conditions-especially by matrix metalloproteinases-and how it may be targeted for therapeutic benefit.
引用
收藏
页数:10
相关论文
共 113 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]
The ins and Outs of the Epithelial to Mesenchymal Transition in Health and Disease [J].
Angela Nieto, M. .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, VOL 27, 2011, 27 :347-376
[3]
TGFβ/TNFα-Mediated Epithelial-Mesenchymal Transition Generates Breast Cancer Stem Cells with a Claudin-Low Phenotype [J].
Asiedu, Michael K. ;
Ingle, James N. ;
Behrens, Marshall D. ;
Radisky, Derek C. ;
Knutson, Keith L. .
CANCER RESEARCH, 2011, 71 (13) :4707-4719
[4]
The Snail genes as inducers of cell movement and survival: implications in development and cancer [J].
Barrallo-Gimeno, A ;
Nieto, MA .
DEVELOPMENT, 2005, 132 (14) :3151-3161
[5]
BARTOW SA, 1990, CANCER-AM CANCER SOC, V66, P1721, DOI 10.1002/1097-0142(19901015)66:8<1721::AID-CNCR2820660812>3.0.CO
[6]
2-I
[7]
Putting tumours in context [J].
Bissell, MJ ;
Radisky, D .
NATURE REVIEWS CANCER, 2001, 1 (01) :46-54
[8]
Mammographic breast density as an intermediate phenotype for breast cancer [J].
Boyd, NF ;
Rommens, JM ;
Vogt, K ;
Lee, V ;
Hopper, JL ;
Yaffe, MJ ;
Paterson, AD .
LANCET ONCOLOGY, 2005, 6 (10) :798-808
[9]
Mammographic densities and the prevalence and incidence of histological types of benign breast disease [J].
Boyd, NF ;
Jensen, HM ;
Cooke, G ;
Han, HL ;
Lockwood, GA ;
Miller, AB .
EUROPEAN JOURNAL OF CANCER PREVENTION, 2000, 9 (01) :15-24
[10]
BRIGHT RA, 1988, CANCER-AM CANCER SOC, V61, P266, DOI 10.1002/1097-0142(19880115)61:2<266::AID-CNCR2820610212>3.0.CO