Literature DB >> 26131648

Chick Heart Invasion Assay for Testing the Invasiveness of Cancer Cells and the Activity of Potentially Anti-invasive Compounds.

Marc E Bracke1, Bart I Roman2, Christian V Stevens2, Liselot M Mus3, Virinder S Parmar4, Olivier De Wever3, Marc M Mareel3.   

Abstract

The goal of the chick heart assay is to offer a relevant organ culture method to study tumor invasion in three dimensions. The assay can distinguish between invasive and non-invasive cells, and enables study of the effects of test compounds on tumor invasion. Cancer cells - either as aggregates or single cells - are confronted with fragments of embryonic chick heart. After organ culture in suspension for a few days or weeks the confronting cultures are fixed and embedded in paraffin for histological analysis. The three-dimensional interaction between the cancer cells and the normal tissue is then reconstructed from serial sections stained with hematoxylin-eosin or after immunohistochemical staining for epitopes in the heart tissue or the confronting cancer cells. The assay is consistent with the recent concept that cancer invasion is the result of molecular interactions between the cancer cells and their neighbouring stromal host elements (myofibroblasts, endothelial cells, extracellular matrix components, etc.). Here, this stromal environment is offered to the cancer cells as a living tissue fragment. Supporting aspects to the relevance of the assay are multiple. Invasion in the assay is in accordance with the criteria of cancer invasion: progressive occupation and replacement in time and space of the host tissue, and invasiveness and non-invasiveness in vivo of the confronting cells generally correlates with the outcome of the assay. Furthermore, the invasion pattern of cells in vivo, as defined by pathologists, is reflected in the histological images in the assay. Quantitative structure-activity relation (QSAR) analysis of the results obtained with numerous potentially anti-invasive organic congener compounds allowed the study of structure-activity relations for flavonoids and chalcones, and known anti-metastatic drugs used in the clinic (e.g., microtubule inhibitors) inhibit invasion in the assay as well. However, the assay does not take into account immunological contributions to cancer invasion.

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Year:  2015        PMID: 26131648      PMCID: PMC4544965          DOI: 10.3791/52792

Source DB:  PubMed          Journal:  J Vis Exp        ISSN: 1940-087X            Impact factor:   1.355


  25 in total

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Journal:  Curr Opin Cell Biol       Date:  2010-09-06       Impact factor: 8.382

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Authors:  V S Parmar; R Jain; S K Sharma; A Vardhan; A Jha; P Taneja; S Singh; B M Vyncke; M E Bracke; M M Mareel
Journal:  J Pharm Sci       Date:  1994-09       Impact factor: 3.534

7.  Effect of temperature on invasion of MO4 mouse fibrosarcoma cells in organ culture.

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10.  The in ovo CAM-assay as a xenograft model for sarcoma.

Authors:  Gwen M L Sys; Lore Lapeire; Nikita Stevens; Herman Favoreel; Ramses Forsyth; Marc Bracke; Olivier De Wever
Journal:  J Vis Exp       Date:  2013-07-17       Impact factor: 1.355

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  2 in total

Review 1.  Evidence for immortality and autonomy in animal cancer models is often not provided, which causes confusion on key issues of cancer biology.

Authors:  Xixi Dou; Pingzhen Tong; Hai Huang; Lucas Zellmer; Yan He; Qingwen Jia; Daizhou Zhang; Jiang Peng; Chenguang Wang; Ningzhi Xu; Dezhong Joshua Liao
Journal:  J Cancer       Date:  2020-03-04       Impact factor: 4.207

2.  Vehicle development, pharmacokinetics and toxicity of the anti-invasive agent 4-fluoro-3',4',5'-trimethoxychalcone in rodents.

Authors:  Liselot M Mus; Geertrui Denecker; Frank Speleman; Bart I Roman
Journal:  PLoS One       Date:  2018-02-22       Impact factor: 3.240

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