| Literature DB >> 26282170 |
Silja Heilmann1, Kajan Ratnakumar2, Erin Langdon2, Emily Kansler2, Isabella Kim2, Nathaniel R Campbell3, Elizabeth Perry2, Amy McMahon4,5, Charles Kaufman6,7,8,5, Ellen van Rooijen6,7,5, William Lee1, Christine Iacobuzio-Donahue9, Richard Hynes4,5, Leonard Zon6,7,8,5, Joao Xavier1, Richard White2,10.
Abstract
Metastasis is the defining feature of advanced malignancy, yet remains challenging to study in laboratory environments. Here, we describe a high-throughput zebrafish system for comprehensive, in vivo assessment of metastatic biology. First, we generated several stable cell lines from melanomas of transgenic mitfa-BRAF(V600E);p53(-/-) fish. We then transplanted the melanoma cells into the transparent casper strain to enable highly quantitative measurement of the metastatic process at single-cell resolution. Using computational image analysis of the resulting metastases, we generated a metastasis score, μ, that can be applied to quantitative comparison of metastatic capacity between experimental conditions. Furthermore, image analysis also provided estimates of the frequency of metastasis-initiating cells (∼1/120,000 cells). Finally, we determined that the degree of pigmentation is a key feature defining cells with metastatic capability. The small size and rapid generation of progeny combined with superior imaging tools make zebrafish ideal for unbiased high-throughput investigations of cell-intrinsic or microenvironmental modifiers of metastasis. The approaches described here are readily applicable to other tumor types and thus serve to complement studies also employing murine and human cell culture systems. ©2015 American Association for Cancer Research.Entities:
Mesh:
Year: 2015 PMID: 26282170 PMCID: PMC4609292 DOI: 10.1158/0008-5472.CAN-14-3319
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701