Imatinib targeting of KIT-mutant oncoprotein in melanoma
Source: NCBI BioProject (ID PRJNA101057)
Source: NCBI BioProject (ID PRJNA101057)
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Project name: Homo sapiens
Description: Metastatic melanoma is an aggressive treatment-refractory malignancy. Recently, c-Kit mutations were discovered in certain mucosal melanomas. A clinical trial was initiated with the c-Kit inhibitor imatinib mesylate. The first treated patient experienced dramatic clinical improvement within days, followed by major responses by PET/CT four weeks later at all sites of metastatic disease. Several established mucosal melanoma cell lines exhibited imatinib sensitivity in a fashion correlating with c-Kit mutational status. Although c-Kit mutations are uncommon in cutaneous melanoma, they may arise in geographically distinct subsets for whom use of c-Kit targeted kinase inhibition should be considered in a rational therapeutic approach.Keywords: Whole genome copy number analysisOverall design: Copy number analysis using high-density SNP arrays to investigate genetic gains and losses involved in the genesis of mucosal and cutaneous melanoma.GSE8164_raw_copy_number_calls.xls contains raw copy number calls generated by dChip (build 5/2007) for GIST, K008, K029, M34, MEL1, MEL40, M6, and 5 Affymetrix controls (copy number identity 2 i.e. normal), which are available on the HapMAP site.
Data type: Variation
Sample scope: Multiisolate
Relevance: Medical
Organization: Medical Oncology, Dana-Farber Cancer Institute
Literatures
- PMID: 19047099
Release date: 2008-12-24
Last updated: 2007-06-18