Culturing Uveal Melanoma Cells

Abstract

A major challenge in cancer research is the use of appropriate models with which to study a specific biological question. Cell lines have long been used to study cellular processes and the effects of individual molecules because they are easy to use, grow rapidly, produce reproducible results and have a strong track record in research. In uveal melanoma in particular, the absence of animal models that faithfully replicate the behavior of the human disease has propagated the generation and use of numerous cell lines by individual research groups. This in itself, however, can be viewed as a problem due to the lack of standardization when characterizing these entities to determine how closely they reflect the genetic and phenotypic characteristics of this disease. The alternative is to use in vitro primary cultures of cells obtained directly from uveal melanoma patient samples, but this too has its difficulties. Primary cell cultures are difficult to use, hard to obtain and can show considerable heterogeneity. In this article, we review the following: (1) the uveal melanoma cell lines that are currently available, discussing the importance of establishing a bank of those that represent the molecular heterogeneity of uveal melanoma; (2) the methods used to isolate and perform short-term cultures of primary uveal melanoma cells, and (3) the establishment of 3D tissue culture models that bridge the gap between 2D in vitro systems and in vivo models with which to dissect cancer biology and perform therapeutic screens.

Keywords: Culture models; Primary cell cultures; Uveal melanoma.

Fig. 1

Growth rate of isolated primary uveal melanoma cells from a monosomy 3 patient in different media. The cells were grown in either RPMI + 10% FCS, DMEM + 10% FCS, or 1:1 αMEM: Quantum 3-21 + 10% FCS. The cells grew more efficiently in the latter medium and demonstrated the formation of small clumps of cells that could be detached into the medium.