Abstract
With the proliferation of high-throughput technologies to profile the cancer genome, methods to distinguish causal from bystander genetic events are needed. Two recent reports by Zender et al. and Kim et al. in Cell use genetically defined mouse models to serve as biological filters to mine the human cancer genome. Integration of high-resolution copy number profiles of mouse tumor models and human tumors identified cIAP1 and Yap as oncogenes in human hepatocellular carcinoma, while NEDD9 was identified as a metastasis gene in human melanoma. Together, these reports demonstrate that a comparative oncogenomics approach can identify genes causally involved in oncogenesis and metastasis.
Publication types
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Comparative Study
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, Non-P.H.S.
MeSH terms
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Adaptor Proteins, Signal Transducing / genetics
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Animals
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Carcinoma, Hepatocellular / genetics
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Carcinoma, Hepatocellular / pathology
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Cell Cycle Proteins
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Disease Models, Animal
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Genomics / methods*
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Humans
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Inhibitor of Apoptosis Proteins / genetics
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Liver Neoplasms / genetics
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Liver Neoplasms / pathology
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Melanoma / genetics
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Melanoma / pathology
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Mice
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Neoplasm Metastasis
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Neoplasms / genetics*
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Neoplasms / pathology
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Nuclear Proteins / genetics
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Oncogene Proteins / genetics*
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Phosphoproteins / genetics
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Trans-Activators / genetics
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Transcription Factors
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YAP-Signaling Proteins
Substances
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Adaptor Proteins, Signal Transducing
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Cell Cycle Proteins
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Inhibitor of Apoptosis Proteins
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NEDD9 protein, human
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Nuclear Proteins
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Oncogene Proteins
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Phosphoproteins
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Trans-Activators
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Transcription Factors
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YAP-Signaling Proteins
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YY1AP1 protein, human
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Yap1 protein, mouse