» Articles » PMID: 26131648

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

Overview
Journal J Vis Exp
Date 2015 Jul 2
PMID 26131648
Citations 2
Authors
Affiliations
Soon will be listed here.
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.

Citing Articles

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

Dou X, Tong P, Huang H, Zellmer L, He Y, Jia Q J Cancer. 2020; 11(10):2887-2920.

PMID: 32226506 PMC: 7086263. DOI: 10.7150/jca.41324.


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

Mus L, Denecker G, Speleman F, Roman B PLoS One. 2018; 13(2):e0192548.

PMID: 29470507 PMC: 5823406. DOI: 10.1371/journal.pone.0192548.

References
1.
Parmar V, Bracke M, Philippe J, Wengel J, Jain S, Olsen C . Anti-invasive activity of alkaloids and polyphenolics in vitro. Bioorg Med Chem. 1997; 5(8):1609-19. DOI: 10.1016/s0968-0896(97)00091-6. View

2.
Mareel M, KINT J, Meyvisch C . Methods of study of the invasion of malignant C3H-mouse fibroblasts into embryonic chick heart in vitro. Virchows Arch B Cell Pathol Incl Mol Pathol. 1979; 30(1):95-111. DOI: 10.1007/BF02889094. View

3.
Schleich A, Frick M, Mayer A . Patterns of invasive growth in vitro. Human decidua graviditatis confronted with established human cell lines and primary human explants. J Natl Cancer Inst. 1976; 56(2):221-37. DOI: 10.1093/jnci/56.2.221. View

4.
Sys G, Lapeire L, Stevens N, Favoreel H, Forsyth R, Bracke M . The in ovo CAM-assay as a xenograft model for sarcoma. J Vis Exp. 2013; (77):e50522. PMC: 3845689. DOI: 10.3791/50522. View

5.
Bjerkvig R, Laerum O, Mella O . Glioma cell interactions with fetal rat brain aggregates in vitro and with brain tissue in vivo. Cancer Res. 1986; 46(8):4071-9. View