Epithelial-mesenchymal and mesenchymal-epithelial transitions in carcinoma progression
Like a set of bookends, cellular, molecular, and genetic changes of the beginnings of life mirror those of one of the most common cause of death—metastatic cancer. Epithelial to mesenchymal transition (EMT) is an important change in cell phenotype which allows the escape of epithelial cells from the...
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Published in | Journal of cellular physiology Vol. 213; no. 2; pp. 374 - 383 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Hoboken
Wiley Subscription Services, Inc., A Wiley Company
01.11.2007
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Subjects | |
Online Access | Get full text |
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Abstract | Like a set of bookends, cellular, molecular, and genetic changes of the beginnings of life mirror those of one of the most common cause of death—metastatic cancer. Epithelial to mesenchymal transition (EMT) is an important change in cell phenotype which allows the escape of epithelial cells from the structural constraints imposed by tissue architecture, and was first recognized by Elizabeth Hay in the early to mid 1980's to be a central process in early embryonic morphogenesis. Reversals of these changes, termed mesenchymal to epithelial transitions (METs), also occur and are important in tissue construction in normal development. Over the last decade, evidence has mounted for EMT as the means through which solid tissue epithelial cancers invade and metastasize. However, demonstrating this potentially rapid and transient process in vivo has proven difficult and data connecting the relevance of this process to tumor progression is still somewhat limited and controversial. Evidence for an important role of MET in the development of clinically overt metastases is starting to accumulate, and model systems have been developed. This review details recent advances in the knowledge of EMT as it occurs in breast development and carcinoma and prostate cancer progression, and highlights the role that MET plays in cancer metastasis. Finally, perspectives from a clinical and translational viewpoint are discussed. J. Cell. Physiol. 213: 374–383, 2007. © 2007 Wiley‐Liss, Inc. |
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AbstractList | Like a set of bookends, cellular, molecular, and genetic changes of the beginnings of life mirror those of one of the most common cause of death—metastatic cancer. Epithelial to mesenchymal transition (EMT) is an important change in cell phenotype which allows the escape of epithelial cells from the structural constraints imposed by tissue architecture, and was first recognized by Elizabeth Hay in the early to mid 1980's to be a central process in early embryonic morphogenesis. Reversals of these changes, termed mesenchymal to epithelial transitions (METs), also occur and are important in tissue construction in normal development. Over the last decade, evidence has mounted for EMT as the means through which solid tissue epithelial cancers invade and metastasize. However, demonstrating this potentially rapid and transient process in vivo has proven difficult and data connecting the relevance of this process to tumor progression is still somewhat limited and controversial. Evidence for an important role of MET in the development of clinically overt metastases is starting to accumulate, and model systems have been developed. This review details recent advances in the knowledge of EMT as it occurs in breast development and carcinoma and prostate cancer progression, and highlights the role that MET plays in cancer metastasis. Finally, perspectives from a clinical and translational viewpoint are discussed. J. Cell. Physiol. 213: 374–383, 2007. © 2007 Wiley‐Liss, Inc. Like a set of bookends, cellular, molecular, and genetic changes of the beginnings of life mirror those of one of the most common cause of death--metastatic cancer. Epithelial to mesenchymal transition (EMT) is an important change in cell phenotype which allows the escape of epithelial cells from the structural constraints imposed by tissue architecture, and was first recognized by Elizabeth Hay in the early to mid 1980's to be a central process in early embryonic morphogenesis. Reversals of these changes, termed mesenchymal to epithelial transitions (METs), also occur and are important in tissue construction in normal development. Over the last decade, evidence has mounted for EMT as the means through which solid tissue epithelial cancers invade and metastasize. However, demonstrating this potentially rapid and transient process in vivo has proven difficult and data connecting the relevance of this process to tumor progression is still somewhat limited and controversial. Evidence for an important role of MET in the development of clinically overt metastases is starting to accumulate, and model systems have been developed. This review details recent advances in the knowledge of EMT as it occurs in breast development and carcinoma and prostate cancer progression, and highlights the role that MET plays in cancer metastasis. Finally, perspectives from a clinical and translational viewpoint are discussed. |
Author | Lawrence, Mitchell G. Williams, Elizabeth D. Thompson, Erik W. Blick, Tony Clements, Judith A. Hugo, Honor Ackland, M. Leigh |
Author_xml | – sequence: 1 givenname: Honor surname: Hugo fullname: Hugo, Honor organization: Embryology Laboratory, Murdoch Children's Research Institute, The Royal Children's Hospital, Victoria, Australia – sequence: 2 givenname: M. Leigh surname: Ackland fullname: Ackland, M. Leigh organization: Centre for Cellular and Molecular Biology, Deakin University, Victoria, Australia – sequence: 3 givenname: Tony surname: Blick fullname: Blick, Tony organization: VBCRC Invasion and Metastasis Unit, St. Vincent's Institute, Victoria, Australia – sequence: 4 givenname: Mitchell G. surname: Lawrence fullname: Lawrence, Mitchell G. organization: School of Life Sciences and Institute of Health and Biomedical Innovation, Queensland University of Technology, Queensland, Australia – sequence: 5 givenname: Judith A. surname: Clements fullname: Clements, Judith A. organization: Centre for Cancer Research, Monash Institute of Medical Research, Monash University, Victoria, Australia – sequence: 6 givenname: Elizabeth D. surname: Williams fullname: Williams, Elizabeth D. email: elizabeth.williams@med.monash.edu.au organization: Centre for Cancer Research, Monash Institute of Medical Research, Monash University, Victoria, Australia – sequence: 7 givenname: Erik W. surname: Thompson fullname: Thompson, Erik W. organization: The University of Melbourne Department of Surgery, St. Vincent's Hospital, Victoria, Australia |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/17680632$$D View this record in MEDLINE/PubMed |
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SubjectTerms | Biomarkers - metabolism Breast Neoplasms Carcinoma - pathology Carcinoma - physiopathology Cell Line, Tumor Cell Transformation, Neoplastic Disease Progression Epithelial Cells - cytology Epithelial Cells - metabolism Epithelium - pathology Epithelium - physiology Female Humans Male Mesoderm - pathology Mesoderm - physiology Neoplasm Invasiveness Prostatic Neoplasms - pathology Prostatic Neoplasms - physiopathology |
Title | Epithelial-mesenchymal and mesenchymal-epithelial transitions in carcinoma progression |
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