The B-RAF kinase is a downstream effector of the RAS family of proto-oncogenes and is constitutively activated in the majority of human melanomas. The common oncogenic B-RAF V600E mutant cooperates with additional genetic lesions to transform immortal murine and human cells. In primary cells, however, B-RAF V600E triggers a rapid cell cycle arrest that is phenotypically indistinguishable from cellular senescence. Here we describe the analyses of B-RAF-induced senescence in primary human melanocytes using recombinant lentiviruses. © Springer Science+Business Media New York 2013.
CITATION STYLE
Tran, S. L., & Rizos, H. (2013). Monitoring oncogenic B-RAF-induced senescence in melanocytes. Methods in Molecular Biology, 965, 313–326. https://doi.org/10.1007/978-1-62703-239-1_21
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