E-viri
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Thu, Kelsie L; Papari-Zareei, Mahboubeh; Stastny, Victor; Song, Kai; Peyton, Michael; Martinez, Victor D; Zhang, Yu-An; Castro, Isabel B; Varella-Garcia, Marileila; Liang, Hanquan; Xing, Chao; Kittler, Ralf; Milchgrub, Sara; Castrillon, Diego H; Davidson, Heather L; Reynolds, C Patrick; Lam, Wan L; Lea, Jayanthi; Gazdar, Adi F
Oncotarget, 08/2017, Letnik: 8, Številka: 31Journal Article
Recent literature suggests that most widely used ovarian cancer (OVCA) cell models do not recapitulate the molecular features of clinical tumors. To address this limitation, we generated 18 cell lines and 3 corresponding patient-derived xenografts predominantly from high-grade serous carcinoma (HGSOC) peritoneal effusions. Comprehensive genomic characterization and comparison of each model to its parental tumor demonstrated a high degree of molecular similarity. Our characterization included whole exome-sequencing and copy number profiling for cell lines, xenografts, and matched non-malignant tissues, and DNA methylation, gene expression, and spectral karyotyping for a subset of specimens. Compared to the Cancer Genome Atlas (TCGA), our models more closely resembled HGSOC than any other tumor type, justifying their validity as OVCA models. Our meticulously characterized models provide a crucial resource for the OVCA research community that will advance translational findings and ultimately lead to clinical applications.
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JCR | SNIP | JCR | SNIP | JCR | SNIP | JCR | SNIP |
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Vir: Osebne bibliografije
in: SICRIS
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