The gene expression signatures of melanoma progression
Author(s) -
Christopher M. Haqq,
Mehdi Nosrati,
Daniel Sudilovsky,
Julia Crothers,
Daniel Khodabakhsh,
Brian Pulliam,
Scot Federman,
James R. Miller,
Robert E. Allen,
Mark I. Singer,
Stanley P. L. Leong,
BrittMarie Ljung,
Richard W. Sagebiel,
Mohammed KashaniSabet
Publication year - 2005
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.0501564102
Subject(s) - melanoma , gene expression , dna microarray , gene , biology , significance analysis of microarrays , pathology , gene expression profiling , primary tumor , cancer research , cancer , medicine , metastasis , genetics
Because of the paucity of available tissue, little information has previously been available regarding the gene expression profiles of primary melanomas. To understand the molecular basis of melanoma progression, we compared the gene expression profiles of a series of nevi, primary melanomas, and melanoma metastases. We found that metastatic melanomas exhibit two dichotomous patterns of gene expression, which unexpectedly reflect gene expression differences already apparent in comparing laser-capture microdissected radial and vertical phases of a large primary melanoma. Unsupervised hierarchical clustering accurately separated nevi and primary melanomas. Multiclass significance analysis of microarrays comparing normal skin, nevi, primary melanomas, and the two types of metastatic melanoma identified 2,602 transcripts that significantly correlated with sample class. These results suggest that melanoma pathogenesis can be understood as a series of distinct molecular events. The gene expression signatures identified here provide the basis for developing new diagnostics and targeting therapies for patients with malignant melanoma.
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