Literature DB >> 11477573

Quantitative cell dispersion analysis: new test to measure tumor cell aggressiveness.

B Nawrocki Raby1, M Polette, C Gilles, C Clavel, K Strumane, M Matos, J M Zahm, F Van Roy, N Bonnet, P Birembaut.   

Abstract

Tumor progression requires the dispersion of epithelial cells from neoplastic clusters and cell invasion of adjacent stromal connective tissue. Aiming at demonstrating the precise relationships between cell dispersion and cell invasion, related respectively to expression of E-cadherin/catenin complex and matrix metalloproteinases (MMPs), we developed an original in vitro model of cell dispersion analysis. Our study reports the validation of this model that allowed us to analyze and quantify the cell cohesion level by means of time-lapse videomicroscopy and computer analysis based on the observation of spatial and temporal cell distribution. Our model was able to distinguish 2 groups among different human bronchial and mammary epithelial cells previously characterized for the expression of E-cadherin/catenin complex and MMPs and their invasive capacity in the Boyden chamber assay. The first group (16HBE14o(-), MCF-7, T47D) that expressed membranous E-cadherin and beta-catenin, and was negative for MMP-2 expression and non-invasive, displayed a highly cohesive pattern corresponding to a cluster spatial distribution. The second group (Beas2B, BZR, BZR-T33, MDA-MB-231, MDA-MB-435, BT549 and HS578T) that was invasive and showed lack of expression of E-cadherin and a cytoplasmic redistribution of beta-catenin, displayed a dispersed pattern corresponding to a random spatial distribution. Downregulation of E-cadherin by a blocking antibody induced a more random distribution. Conversely, expression of E-cadherin by cDNA transfection induced a cluster distribution. Moreover, tumor cell lines that co-expressed MT1-MMP and MMP-2 (Beas2B, BZR, BZR-T33, MDA-MB-435, BT549 and HS578T) showed a more dispersed pattern than tumor cell lines that did not express MMP-2 (MDA-MB-231). In conclusion, we demonstrated that the spatial group behavior of cell lines, i.e., their cohesion/dispersion ability, reflects their invasive properties. Thus, this model of cell dispersion analysis may represent a new test to measure tumor cell aggressiveness. Copyright 2001 Wiley-Liss, Inc.

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Year:  2001        PMID: 11477573     DOI: 10.1002/ijc.1380

Source DB:  PubMed          Journal:  Int J Cancer        ISSN: 0020-7136            Impact factor:   7.396


  12 in total

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Journal:  Int J Cancer       Date:  2006-01-01       Impact factor: 7.396

2.  Morphologic and molecular events at the invading edge of colorectal carcinomas.

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3.  The biological relevance of laminin 5gamma2 expression at the invading edge of colonic carcinomas.

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4.  E-Cadherin mediates MMP down-regulation in highly invasive bronchial tumor cells.

Authors:  Béatrice Nawrocki-Raby; Christine Gilles; Myriam Polette; Corinne Martinella-Catusse; Noël Bonnet; Edith Puchelle; Jean-Michel Foidart; Frans Van Roy; Philippe Birembaut
Journal:  Am J Pathol       Date:  2003-08       Impact factor: 4.307

5.  Phenotypic reversion or death of cancer cells by altering signaling pathways in three-dimensional contexts.

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6.  Loss of the Metastasis Suppressor NME1, But Not of Its Highly Related Isoform NME2, Induces a Hybrid Epithelial-Mesenchymal State in Cancer Cells.

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7.  c-Abl and Arg are activated in human primary melanomas, promote melanoma cell invasion via distinct pathways, and drive metastatic progression.

Authors:  S S Ganguly; L S Fiore; J T Sims; J W Friend; D Srinivasan; M A Thacker; M L Cibull; C Wang; M Novak; D M Kaetzel; R Plattner
Journal:  Oncogene       Date:  2011-09-05       Impact factor: 9.867

8.  Epigallocatechin-3-gallate (EGCG) inhibits the migratory behavior of tumor bronchial epithelial cells.

Authors:  Salma Hazgui; Arnaud Bonnomet; Béatrice Nawrocki-Raby; Magali Milliot; Christine Terryn; Jérôme Cutrona; Myriam Polette; Philippe Birembaut; Jean-Marie Zahm
Journal:  Respir Res       Date:  2008-04-21

9.  Quantification of topological features in cell meshes to explore E-cadherin dysfunction.

Authors:  Tânia Mestre; Joana Figueiredo; Ana Sofia Ribeiro; Joana Paredes; Raquel Seruca; João Miguel Sanches
Journal:  Sci Rep       Date:  2016-05-06       Impact factor: 4.379

10.  The Role of Desmoplasia and Stromal Fibroblasts on Anti-cancer Drug Resistance in a Microengineered Tumor Model.

Authors:  Harpinder Saini; Kiarash Rahmani Eliato; Casey Silva; Mayar Allam; Ghassan Mouneimne; Robert Ros; Mehdi Nikkhah
Journal:  Cell Mol Bioeng       Date:  2018-07-31       Impact factor: 2.321

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