Comparative oncogenomics identifies NEDD9 as a melanoma metastasis gene.

TitleComparative oncogenomics identifies NEDD9 as a melanoma metastasis gene.
Publication TypeJournal Article
Year of Publication2006
AuthorsKim M, Gans JD, Nogueira C, Wang A, Paik J-H, Feng B, Brennan C, Hahn WC, Cordon-Cardo C, Wagner SN, Flotte TJ, Duncan LM, Granter SR, Chin L
JournalCell
Volume125
Issue7
Pagination1269-81
Date Published2006 Jun 30
ISSN0092-8674
KeywordsAdaptor Proteins, Signal Transducing, Animals, Base Sequence, DNA, Neoplasm, Female, Focal Adhesion Kinase 1, Gene Amplification, Gene Expression, Genomics, Humans, In Vitro Techniques, Melanocytes, Melanoma, Melanoma, Experimental, Mice, Mice, Knockout, Mice, SCID, Neoplasm Invasiveness, Oncogenes, Phosphoproteins, RNA Interference, Species Specificity
Abstract

Genomes of human cancer cells are characterized by numerous chromosomal aberrations of uncertain pathogenetic significance. Here, in an inducible mouse model of melanoma, we characterized metastatic variants with an acquired focal chromosomal amplification that corresponds to a much larger amplification in human metastatic melanomas. Further analyses identified Nedd9, an adaptor protein related to p130CAS, as the only gene within the minimal common region that exhibited amplification-associated overexpression. A series of functional, biochemical, and clinical studies established NEDD9 as a bona fide melanoma metastasis gene. NEDD9 enhanced invasion in vitro and metastasis in vivo of both normal and transformed melanocytes, functionally interacted with focal adhesion kinase and modulated focal contact formation, and exhibited frequent robust overexpression in human metastatic melanoma relative to primary melanoma. Thus, comparative oncogenomics has enabled the identification and facilitated the validation of a highly relevant cancer gene governing metastatic potential in human melanoma.

DOI10.1016/j.cell.2006.06.008
Alternate JournalCell
PubMed ID16814714
Grant ListP50 CA093683 / CA / NCI NIH HHS / United States
U01 CA105423 / CA / NCI NIH HHS / United States
U01 CA84313 / CA / NCI NIH HHS / United States
P50 CA93683 / CA / NCI NIH HHS / United States
P50 CA112962 / CA / NCI NIH HHS / United States
R01 CA93947 / CA / NCI NIH HHS / United States
Related Faculty: 
Ji-Hye Paik, Ph.D.

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