TY - CHAP
T1 - Establishment of two dimensional (2D) and three-dimensional (3D) melanoma primary cultures as a tool for in vitro drug resistance studies
AU - Cruz Rodríguez, Nataly
AU - Lineros, Johanna
AU - Rodríguez, Carol Stefany
AU - Martínez, Lina María
AU - Rodríguez, Josefa Antonia
N1 - Publisher Copyright:
© Springer Science+Business Media, LLC, part of Springer Nature 2019.
PY - 2019
Y1 - 2019
N2 - Characteristics of melanoma cells have been deciphered by studies carried out in two dimensional cell cultures growing as adherent monolayers on the bottom of plastic flasks. Melanoma cells can be cultured with a considerable degree of success, and, depending on the further use of the cells obtained in the culture, methodologies have to be adjusted to obtain reliable results. Although there are many melanoma continuous cell lines, in vitro 2D and 3D melanoma primary cell culture may be a more useful model to investigate interactions between cancer cells and immune system, as well as the effect of cytotoxic treatments and personalized medicine in environments more similar to the physiological conditions. Here, we described a protocol which employs many strategies to obtain primary 2D and 3D melanoma cultures as a model to study cell–cell and cell–microenvironment interactions that must be considered to properly design personalized cancer treatments, as well as for testing novel anticancer drugs and drug delivery vehicles.
AB - Characteristics of melanoma cells have been deciphered by studies carried out in two dimensional cell cultures growing as adherent monolayers on the bottom of plastic flasks. Melanoma cells can be cultured with a considerable degree of success, and, depending on the further use of the cells obtained in the culture, methodologies have to be adjusted to obtain reliable results. Although there are many melanoma continuous cell lines, in vitro 2D and 3D melanoma primary cell culture may be a more useful model to investigate interactions between cancer cells and immune system, as well as the effect of cytotoxic treatments and personalized medicine in environments more similar to the physiological conditions. Here, we described a protocol which employs many strategies to obtain primary 2D and 3D melanoma cultures as a model to study cell–cell and cell–microenvironment interactions that must be considered to properly design personalized cancer treatments, as well as for testing novel anticancer drugs and drug delivery vehicles.
KW - Cancer model
KW - Drug resistance
KW - Melanoma
KW - Primary cell culture
KW - Three-dimensional cell spheroids
KW - Two dimensional cell culture
UR - http://www.scopus.com/inward/record.url?scp=85060218884&partnerID=8YFLogxK
U2 - 10.1007/978-1-4939-8979-9_8
DO - 10.1007/978-1-4939-8979-9_8
M3 - Chapter
C2 - 30666602
AN - SCOPUS:85060218884
T3 - Methods in Molecular Biology
SP - 119
EP - 131
BT - Methods in Molecular Biology
PB - Humana Press Inc.
ER -