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Applications of Genomics in Melanoma Oncogene Discovery
被引:25
|作者:
Berger, Michael F.
[2
]
Garraway, Levi A.
[1
,2
,3
]
机构:
[1] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[2] Broad Inst MIT & Harvard, Cambridge Ctr 7, Cambridge, MA 02142 USA
[3] Dana Farber Canc Inst, Ctr Canc Genome Discovery, Boston, MA 02115 USA
关键词:
Melanoma;
Oncogene;
DNA sequencing;
Microarrays;
Gene amplification;
Targeted therapy;
CUTANEOUS MALIGNANT-MELANOMA;
BLADDER-CARCINOMA ONCOGENE;
N-RAS MUTATIONS;
HUMAN CANCER;
IMATINIB MESYLATE;
METASTATIC MELANOMA;
TRANSFORMING GENES;
BRAF MUTATIONS;
LUNG-CANCER;
COPY NUMBER;
D O I:
10.1016/j.hoc.2009.03.005
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
The identification of recurrent alterations in the melanoma genome has provided key insights into the biology of melanoma genesis and progression. These discoveries have come about as a result of the systematic deployment and integration of diverse genomic technologies, including DNA sequencing, chromosomal copy number analysis, and gene expression profiling. Here, the discoveries of several key melanoma oncogenes affecting critical cell pathways are described and the role played by evolving genomics technologies in melanoma oncogene discovery is examined. These advances are being exploited to improve prognosis and treatment of melanoma patients through the development of genome-based diagnostic and targeted therapeutic avenues.
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页码:397 / +
页数:19
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