Journal article
Integrated genome-wide DMA copy number and expression analysis identifies distinct mechanisms of primary chemoresistance in ovarian carcinomas
D Etemadmoghadam, A Defazio, R Beroukhim, C Mermel, J George, G Getz, R Tothiil, A Okamoto, MB Raeder, P Harnett, S Lade, LA Akslen, AV Tinker, B Locandro, K Aisop, YE Chiew, N Traficante, S Fereday, D Johnson, S Fox Show all
Clinical Cancer Research | Published : 2009
Abstract
Purpose; A significant number of women with serous ovarian cancer are intrinsically refractory to platinum-based treatment. We analyzed somatic DIM A copy number variation and gene expression data to identify key mechanisms associated with primary resistance in advanced- stage serous cancers. Experimental Design: Genome-wide copy number variation was measured in 118 ovarian tumors using high-resolution oligonucleotide microarrays. A well-defined subset of 85 advanced-stage serous tumors was then used to relate copy number variation to primary resistance to treatment. The discovery-based approach was complemented by quantitative-PCR copy number analysis of 12 candidate genes as independent va..
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Awarded by National Institute of General Medical Sciences
Funding Acknowledgements
U.S. Army Medical Research and Materiel Command under DAMD17-01-1-0729, The Cancer Council Victoria, Queensland Cancer Fund, The Cancer Council New South Wales, The Cancer Council South Australia, The Cancer Foundation of Western Australia, The Cancer Council Tasmania and the National Health and Medical Research Council of Australia (NHMRC), the U.S. Department of Defense grant PC040638 and the Dana-Farber/Harvard Cancer Center Prostate SPORE.