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Published in: Cancer and Metastasis Reviews 1-2/2012

01-06-2012 | NON-THEMATIC REVIEW

Cooperate concept of metastasis: site-specific requirement of activated differentiation and dynamic deterioration

Authors: C. Wilmanns, S. Steinhauer, J. Großmann, A. Schmitt-Gräff, G. Ruf

Published in: Cancer and Metastasis Reviews | Issue 1-2/2012

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Abstract

Cancer metastasis results from positive and negative cellular events such as constitutive activation of oncogenes (cOA) or genetic losses (GL) being modulated by downstream signals of epithelial–mesenchymal or mesenchymal–epithelial transition, thus constituting master programs of metastatic phenotype and site specificity. To address the complex nature of these programs, we introduced clinical and phenotypic markers like tumor size, grade, cellular shape, or expression of E-cadherin in 27 colon cancer (CC) patients (cOA and GL), and 41 patients with gastrointestinal stromal tumors (GIST, cOA) to produce scores of cOA and GL. Scores of cOA were highest in case of hepatic and lower in case of an isolated peritoneal spread (GIST), or (CC) of both, cOA and GL, highest in case of a combined hepatic and peritoneal spread and lower in case of an isolated peritoneal spread; but in case of an isolated hepatic spread, scores of cOA were high and low of GL. This indicates a differential contribution of cellular dissociation and recognition in site-specific metastasis, of cOA predominantly in production of hepatic and in the case of GL of serosal spread.
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Metadata
Title
Cooperate concept of metastasis: site-specific requirement of activated differentiation and dynamic deterioration
Authors
C. Wilmanns
S. Steinhauer
J. Großmann
A. Schmitt-Gräff
G. Ruf
Publication date
01-06-2012
Publisher
Springer US
Published in
Cancer and Metastasis Reviews / Issue 1-2/2012
Print ISSN: 0167-7659
Electronic ISSN: 1573-7233
DOI
https://doi.org/10.1007/s10555-012-9350-3

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