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Quantitative Analysis of Human Cancer Cell Extravasation Using Intravital Imaging

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The Tumor Microenvironment

Part of the book series: Methods in Molecular Biology ((MIMB,volume 1458))

Abstract

Metastasis, or the spread of cancer cells from a primary tumor to distant sites, is the leading cause of cancer-associated death. Metastasis is a complex multi-step process comprised of invasion, intravasation, survival in circulation, extravasation, and formation of metastatic colonies. Currently, in vitro assays are limited in their ability to investigate these intricate processes and do not faithfully reflect metastasis as it occurs in vivo. Traditional in vivo models of metastasis are limited by their ability to visualize the seemingly sporadic behavior of where and when cancer cells spread (Reymond et al., Nat Rev Cancer 13:858–870, 2013). The avian embryo model of metastasis is a powerful platform to study many of the critical steps in the metastatic cascade including the migration, extravasation, and invasion of human cancer cells in vivo (Sung et al., Nat Commun 6:7164, 2015; Leong et al., Cell Rep 8, 1558–1570, 2014; Kain et al., Dev Dyn 243:216–28, 2014; Leong et al., Nat Protoc 5:1406–17, 2010; Zijlstra et al., Cancer Cell 13:221–234, 2008; Palmer et al., J Vis Exp 51:2815, 2011). The chicken chorioallantoic membrane (CAM) is a readily accessible and well-vascularized tissue that surrounds the developing embryo. When the chicken embryo is grown in a shell-less, ex ovo environment, the nearly transparent CAM provides an ideal environment for high-resolution fluorescent microcopy approaches. In this model, the embryonic chicken vasculature and labeled cancer cells can be visualized simultaneously to investigate specific steps in the metastatic cascade including extravasation. When combined with the proper image analysis tools, the ex ovo chicken embryo model offers a cost-effective and high-throughput platform for the quantitative analysis of tumor cell metastasis in a physiologically relevant in vivo setting. Here we discuss detailed procedures to quantify cancer cell extravasation in the shell-less chicken embryo model with advanced fluorescence microscopy techniques.

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References

  1. Reymond N, d’Agua BB, Ridley AA (2013) Crossing the endothelial barrier during metastasis. Nat Rev Cancer 13:858–870

    Article  CAS  PubMed  Google Scholar 

  2. Sung BH, Ketova T, Hoshino D, Zijlstra A, Weaver AM (2015) Directional cell movement through tissues is controlled by exosome secretion. Nat Commun 6:7164

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  3. Leong HS, Robertson AE, Stoletov K, Leith SJ, Chin CA, Chien AE et al (2014) Invadopodia are required for cancer cell extravasation and are a therapeutic target for metastasis. Cell Rep 8:1558–1570

    Article  CAS  PubMed  Google Scholar 

  4. Kain KH, Miller JW, Jones-Paris CR, Thomason RT, Lewis JD, Bader DM et al (2014) The chick embryo as an expanding experimental model for cancer and cardiovascular research. Dev Dyn 243:216–228

    Article  PubMed  Google Scholar 

  5. Leong HS, Steinmetz NF, Ablack A, Destito G, Zijlstra A, Stuhlmann H et al (2010) Intravital imaging of embryonic and tumor neovasculature using viral nanoparticles. Nat Protoc 5:1406–1417

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  6. Zijlstra A, Lewis J, Degryse B, Stuhlmann H, Quigley JP (2008) The inhibition of tumor cell intravasation and subsequent metastasis via regulation of in vivo tumor cell motility by the tetraspanin CD151. Cancer Cell 13:221–234

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  7. Palmer TD, Lewis J, Zijlstra A (2011) Quantitative analysis of cancer metastasis using an avian embryo model. J Vis Exp 51:2815

    Google Scholar 

  8. Hanahan D, Weinberg RA (2000) The hallmarks of cancer. Cell 100:57–70

    Article  CAS  PubMed  Google Scholar 

  9. van’t Veer LJ, Dai H, van de Vijver MJ, He YD, Hart AA, Mao M et al (2002) Gene expression profiling predicts clinical outcome of breast cancer. Nature 415:530–536

    Article  Google Scholar 

  10. Eccles SA, Welch DR (2007) Metastasis: recent discoveries and novel treatment strategies. Lancet 369:1742–1757

    Article  CAS  PubMed Central  Google Scholar 

  11. Weber GF (2008) Molecular mechanisms of metastasis. Cancer Lett 270:181–190

    Article  CAS  PubMed  Google Scholar 

  12. Fidler IJ (2001) Seed and soil revisited: contribution of the organ microenvironment to cancer metastasis. Surg Oncol Clin N Am 10:257–269

    CAS  PubMed  Google Scholar 

  13. Chambers AF, Groom AC, MacDonald IC (2002) Dissemination and growth of cancer cells in metastatic sites. Nat Rev Cancer 2:563–572

    Article  CAS  PubMed  Google Scholar 

  14. Pantel K, Brakenhoff RH (2004) Dissecting the metastatic cascade. Nat Rev Cancer 4:448–456

    Article  CAS  PubMed  Google Scholar 

  15. Friedl P, Wolf K (2003) Tumour-cell invasion and migration: diversity and escape mechanisms. Nat Rev Cancer 3:362–374

    Article  CAS  PubMed  Google Scholar 

  16. Stoletov K, Lewis JD (2015) Invadopodia: a new therapeutic target to block cancer metastasis. Expert Rev Anticancer Ther 15:733–735

    Article  CAS  PubMed  Google Scholar 

  17. Leong HS, Chambers AF, Lewis JD (2012) Assessing cancer cell migration and metastatic growth in vivo in the chick embryo using fluorescence intravital imaging. Methods Mol Biol 872:1–14

    Article  CAS  PubMed  Google Scholar 

  18. Leighton J (1964) Invasion and metastasis of heterologous tumors in the chick embryo. Prog Exp Tumor Res 4:98–125

    Article  CAS  PubMed  Google Scholar 

  19. Locker J, Goldblatt PJ, Leighton J (1969) Hematogenous metastasis of Yoshida ascites Hepatoma in the chick embryo liver: ultrastructural changes in tumor cells. Cancer Res 29:1245–1253

    CAS  PubMed  Google Scholar 

  20. McAllister RM, Peer M, Gilden RV, Landing BH (1974) Tumors formed by human rhabdomyosarcoma cells in chorioallantoic membrane of embryonated hens’ eggs. Int J Cancer 13:886–890

    Article  CAS  PubMed  Google Scholar 

  21. Chambers AF, Shafir R, Ling V (1982) A model system for studying metastasis using the embryonic chick. Cancer Res 42:4018–4025

    CAS  PubMed  Google Scholar 

  22. Chambers AF, Wilson S (1985) Cells transformed with a ts viral src mutant are temperature sensitive for in vivo growth. Mol Cell Biol 5:728–733

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  23. Gordon JR, Quigley JP (1986) Early spontaneous metastasis in the human epidermoid carcinoma HEp3/chick embryo model: contribution of incidental colonization. Int J Cancer 38:437–444

    Article  CAS  PubMed  Google Scholar 

  24. Chambers AF, Schmidt EE, MacDonald IC, Morris VL, Groom AC (1992) Early steps in hematogenous metastasis of B16F1 melanoma cells in chick embryos studied by high-resolution intravital videomicroscopy. J Natl Cancer Inst 84:797–803

    Article  CAS  PubMed  Google Scholar 

  25. Quigley JP, Armstrong PB (1998) Tumor cell intravasation elucidated: the chick embryo opens the window. Cell 94:281–284

    Article  CAS  PubMed  Google Scholar 

  26. MacDonald IC, Schmidt EE, Morris VL, Chambers AF, Groom AC (1992) Intravital videomicroscopy of the chorioallantoic microcirculation: a model system for studying metastasis. Microvasc Res 44:185–199

    Article  CAS  PubMed  Google Scholar 

  27. Aguirre-Ghiso JA, Ossowski L, Rosenbaum SK (2004) Green fluorescent protein tagging of extracellular signal-regulated kinase and p38 pathways reveals novel dynamics of pathway activation during primary and metastatic growth. Cancer Res 64:7336–7345

    Article  CAS  PubMed  Google Scholar 

  28. Wilson SM, Chambers AF (2004) Experimental metastasis assays in the chick embryo. Curr Protoc Cell Biol Chapter 19:Unit 19 6

    Google Scholar 

  29. Pink DB, Schulte W, Parseghian MH, Zijlstra A, Lewis JD (2012) Real-time visualization and quantitation of vascular permeability in vivo: implications for drug delivery. PLoS One 7:e33760

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  30. Cho CF, Ablack A, Leong HS, Zijlstra A, Lewis JD (2011) Evaluation of nanoparticle uptake in tumors in real time using intravital imaging. J Vis Exp 52:2808

    PubMed  Google Scholar 

  31. Deryugina EI, Quigley JP (2008) Chick embryo chorioallantoic membrane model systems to study and visualize human tumor cell metastasis. Histochem Cell Biol 130:1119–1130

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  32. Chishima T, Miyagi Y, Wang X, Yamaoka H, Shimada H, Moossa AR, Hoffman RM (1997) Cancer invasion and micrometastasis visualized in live tissue by green fluorescent protein expression. Cancer Res 57:2042–2047

    CAS  PubMed  Google Scholar 

  33. Naumov GN, Wilson SM, MacDonald IC, Schmidt EE, Morris VL, Groom AC et al (1999) Cellular expression of green fluorescent protein, coupled with high-resolution in vivo videomicroscopy, to monitor steps in tumor metastasis. J Cell Sci 112:1835–1842

    CAS  PubMed  Google Scholar 

  34. Lewis JD, Destito G, Zijlstra A, Gonzalez MJ, Quigley JP, Manchester M et al (2006) Viral nanoparticles as tools for intravital vascular imaging. Nat Med 12:354–360

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  35. Sahai E (2007) Illuminating the metastatic process. Nat Rev Cancer 7:737–749

    Article  CAS  PubMed  Google Scholar 

  36. Hoffman RM (2009) Imaging cancer dynamics in vivo at the tumor and cellular level with fluorescent proteins. Clin Exp Metastasis 26:345–355

    Article  CAS  PubMed  Google Scholar 

  37. Hoffman RM (2005) The multiple uses of fluorescent proteins to visualize cancer in vivo. Nat Rev Cancer 5:796–806

    Article  CAS  PubMed  Google Scholar 

  38. Jilani SM, Murphy TJ, Thai SNM, Eichmann A, Alva JA, Irula-Arispe ML (2003) Selective binding of lectins to embryonic chicken vasculature. J Histochem Cytochem 51:597–604

    Article  CAS  PubMed  Google Scholar 

  39. Welch DR (1997) Technical considerations for studying cancer metastasis in vivo. Clin Exp Metastasis 15:272–306

    Article  CAS  PubMed  Google Scholar 

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Acknowledgments

This work was supported by Canadian Cancer Society Research Institute Grant #702849 to J.D.L. and K.S. L.W. and D.B. hold US Department of Defense Prostate Cancer Research Program Postdoctoral Training Awards. D.B. also holds an Alberta Innovates Health Solutions PDF Award. Dr. Lewis holds the Frank and Carla Sojonky Chair in Prostate Cancer Research supported by the Alberta Cancer Foundation. All experiments were performed in accordance with the regulations and guidelines of the Institutional Animal Care and Use Committee at the University of Alberta. We thank Desmond Pink for his photography.

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Correspondence to John D. Lewis Ph.D. .

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Willetts, L., Bond, D., Stoletov, K., Lewis, J.D. (2016). Quantitative Analysis of Human Cancer Cell Extravasation Using Intravital Imaging. In: Ursini-Siegel, J., Beauchemin, N. (eds) The Tumor Microenvironment. Methods in Molecular Biology, vol 1458. Humana Press, New York, NY. https://doi.org/10.1007/978-1-4939-3801-8_3

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  • DOI: https://doi.org/10.1007/978-1-4939-3801-8_3

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