Scientific Publications

Integrative genomic analyses identify MITF as a lineage survival oncogene amplified in malignant melanoma

Publication TypeJournal Article
AuthorsGarraway, Levi A., Widlund Hans R., Rubin Mark A., Getz Gad, Berger Aaron J., Ramaswamy Sridhar, Beroukhim Rameen, Milner Danny A., Granter Scott R., Du Jinyan, Lee Charles, Wagner Stephan N., Li Cheng, Golub Todd R., Rimm David L., Meyerson Matthew L., and Fisher David
AbstractSystematic analyses of cancer genomes promise to unveil patterns of genetic alterations linked to the genesis and spread of human cancers. High-density single-nucleotide polymorphism (SNP) arrays enable detailed and genome-wide identification of both loss-of-heterozygosity events and copy-number alterations in cancer. Here, by integrating SNP array-based genetic maps with gene expression signatures derived from NCI60 cell lines, we identified the melanocyte master regulator MITF (microphthalmia-associated transcription factor) as the target of a novel melanoma amplification. We found that MITF amplification was more prevalent in metastatic disease and correlated with decreased overall patient survival. BRAF mutation and p16 inactivation accompanied MITF amplification in melanoma cell lines. Ectopic MITF expression in conjunction with the BRAF(V600E) mutant transformed primary human melanocytes, and thus MITF can function as a melanoma oncogene. Reduction of MITF activity sensitizes melanoma cells to chemotherapeutic agents. Targeting MITF in combination with BRAF or cyclin-dependent kinase inhibitors may offer a rational therapeutic avenue into melanoma, a highly chemotherapy-resistant neoplasm. Together, these data suggest that MITF represents a distinct class of 'lineage survival' or 'lineage addiction' oncogenes required for both tissue-specific cancer development and tumour progression.
Year of Publication2005
JournalNature
Volume436
Issue7047
Pages117 - 22
Date Published (YYYY/MM/DD)2005/07/07/
ISBN Number1476-4687
KeywordsCancer, Cell Line, Cell Lineage, Cell Survival, Chromosomes, Disease Progression, DNA-Binding Proteins, Fluorescence, Gene Amplification, Gene Dosage, Gene Expression Regulation, Genomics, Human, Humans, In Situ Hybridization, Melanoma, Neoplastic, Pair 3, Tumor