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PMID: 17243120 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Review

Mechanisms of metastasis: epithelial-to-mesenchymal transition and contribution of tumor microenvironment.

Journal of cellular biochemistry ·Vol. 101 ·No. 4 ·2007-07-01 ·Pages 816-29

Tse JC, Kalluri R

Abstract

Every year about 500,000 people in the United States die as a result of cancer. Among them, 90% exhibit systemic disease with metastasis. Considering this high rate of incidence and mortality, it is critical to understand the mechanisms behind metastasis and identify new targets for therapy. In recent years, two broad mechanisms for metastasis have received significant attention: epithelial-to-mesenchymal transition (EMT) and tumor microenvironment interactions. EMT is believed to be a major mechanism by which cancer cells become migratory and invasive. Various cancer cells--both in vivo and in vitro--demonstrate features of epithelial-to-mesenchymal-like transition. In addition, many steps of metastasis are influenced by host contributions from the tumor microenvironment, which help determine the course and severity of metastasis. Here we evaluate the diverse mechanisms of EMT and tumor microenvironment interactions in the progression of cancer, and construct a rational argument for targeting these pathways to control metastasis.

MeSH Terms
Animals Biomarkers, Tumor/analysis Cell Transformation, Neoplastic/metabolism,pathology Epithelial Cells/chemistry,pathology Humans Mesoderm/chemistry,pathology Models, Biological Neoplasm Metastasis
Chemicals
Biomarkers, Tumor
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Tse Joyce C
Division of Matrix Biology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215, USA.
Kalluri Raghu
Article Info
Journal
Journal of cellular biochemistry
Abbr.
J Cell Biochem
ISSN
0730-2312
Published
2007-07-01
Pages
816-29
Language
English
Region
United States
NLM ID
8205768
Subset
IM
Grants
NIAAA NIH HHS · AA13913 · United States
NIDDK NIH HHS · DK55001 · United States
NIDDK NIH HHS · DK61688 · United States
NIDDK NIH HHS · DK62987 · United States
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