Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/12679
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dc.contributor.authorJayachandran, Aparnaen
dc.contributor.authorMcKeown, Sonja Jen
dc.contributor.authorWoods, Briannyn Len
dc.contributor.authorPrithviraj, Prashanthen
dc.contributor.authorCebon, Jonathan Sen
dc.date.accessioned2015-05-16T02:24:26Z
dc.date.available2015-05-16T02:24:26Z
dc.date.issued2015-02-16en
dc.identifier.citationFrontiers in Oncology 2015; 5(): 36en
dc.identifier.govdoc25763357en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/12679en
dc.description.abstractEpithelial-to-mesenchymal transition is a hallmark event in the metastatic cascade conferring invasive ability to tumor cells. There are ongoing efforts to replicate the physiological events occurring during mobilization of tumor cells in model systems. However, few systems are able to capture these complex in vivo events. The embryonic chicken transplantation model has emerged as a useful system to assess melanoma cells including functions that are relevant to the metastatic process, namely invasion and plasticity. The chicken embryo represents an accessible and economical 3-dimensional in vivo model for investigating melanoma cell invasion as it exploits the ancestral relationship between melanoma and its precursor neural crest cells. We describe a methodology that enables the interrogation of melanoma cell motility within the developing avian embryo. This model involves the injection of melanoma cells into the neural tube of chicken embryos. Melanoma cells are labeled using fluorescent tracker dye, Vybrant DiO, then cultured as hanging drops for 24 h to aggregate the cells. Groups of approximately 700 cells are placed into the neural tube of chicken embryos prior to the onset of neural crest migration at the hindbrain level (embryonic day 1.5) or trunk level (embryonic day 2.5). Chick embryos are reincubated and analyzed after 48 h for the location of melanoma cells using fluorescent microscopy on whole mounts and cross-sections of the embryos. Using this system, we compared the in vivo invasive behavior of epithelial-like and mesenchymal-like melanoma cells. We report that the developing embryonic microenvironment confers motile abilities to both types of melanoma cells. Hence, the embryonic chicken transplantation model has the potential to become a valuable tool for in vivo melanoma invasion studies. Importantly, it may provide novel insights into and reveal previously unknown mediators of the metastatic steps of invasion and dissemination in melanoma.en
dc.language.isoenen
dc.subject.otherembryonic chicken transplantationen
dc.subject.otherepithelial-to-mesenchymal transitionen
dc.subject.otherinvasionen
dc.subject.othermelanomaen
dc.subject.otherneural crest cellsen
dc.titleEmbryonic Chicken Transplantation is a Promising Model for Studying the Invasive Behavior of Melanoma Cells.en
dc.typeJournal Articleen
dc.identifier.journaltitleFrontiers in oncologyen
dc.identifier.affiliationCancer Immunobiology Laboratory, Ludwig Institute for Cancer Research, Melbourne-Austin Branch , Heidelberg, VIC , Australia ; Department of Medicine, University of Melbourne , Melbourne, VIC , Australia ; School of Cancer Medicine, La Trobe University , Melbourne, VIC , Australiaen
dc.identifier.affiliationCancer Immunobiology Laboratory, Ludwig Institute for Cancer Research, Melbourne-Austin Branch , Heidelberg, VIC , Australia ; Department of Medicine, University of Melbourne , Melbourne, VIC , Australiaen
dc.identifier.affiliationDepartment of Anatomy and Neuroscience, University of Melbourne , Melbourne, VIC , Australiaen
dc.identifier.doi10.3389/fonc.2015.00036en
dc.description.pages36en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/25763357en
dc.type.austinJournal Articleen
local.name.researcherCebon, Jonathan S
item.fulltextNo Fulltext-
item.languageiso639-1en-
item.grantfulltextnone-
item.openairetypeJournal Article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.deptOlivia Newton-John Cancer Research Institute-
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