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 inJournal of cellular physiology Vol. 213; no. 2; pp. 374 - 383
Main Authors Hugo, Honor, Ackland, M. Leigh, Blick, Tony, Lawrence, Mitchell G., Clements, Judith A., Williams, Elizabeth D., Thompson, Erik W.
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.11.2007
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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.
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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1978; 2
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Snippet 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...
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...
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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
URI https://api.istex.fr/ark:/67375/WNG-LJSVKFTT-Q/fulltext.pdf
https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fjcp.21223
https://www.ncbi.nlm.nih.gov/pubmed/17680632
https://search.proquest.com/docview/68228488
Volume 213
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