| Literature DB >> 25862976 |
Caroline Kreuzinger1, Magdalena Gamperl1, Andrea Wolf1, Georg Heinze2, Angelika Geroldinger2, Diether Lambrechts3, Bram Boeckx3, Dominiek Smeets3, Reinhard Horvat4, Stefanie Aust1, Gerhard Hamilton5, Robert Zeillinger6, Dan Cacsire Castillo-Tong7.
Abstract
Cancer cell lines are good in vitro models to study molecular mechanisms underlying chemoresistance and cancer recurrence. Recent works have demonstrated that most of the available ovarian cancer cell lines are most unlikely high grade serous (HGSOC), the major type of epithelial ovarian cancer. We aimed at establishing well characterized HGSOC cell lines, which can be used as optimal models for ovarian cancer research. We successfully established seven cell lines from HGSOC and provided the major genomic alterations and the transcriptomic landscapes of them. They exhibited different gene expression patterns in the key pathways involved in cancer resistance. Each cell line harbored a unique TP53 mutation as their corresponding tumors and expressed cytokeratins 8/18/19 and EpCAM. Two matched lines were established from the same patient, one at diagnosis and being sensitive to carboplatin and the other during chemotherapy and being resistant. Two cell lines presented respective BRCA1 and BRCA2 mutations. To conclude, we have established seven cell lines and well characterized them at genomic and transcriptomic levels. They are optimal models to investigate the molecular mechanisms underlying the progression, chemo resistance and recurrence of HGSOC.Entities:
Keywords: BRCA; Cell line; High grade serous ovarian cancer; Platinum; TP53
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Year: 2015 PMID: 25862976 DOI: 10.1016/j.canlet.2015.03.040
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679