E-GEOD-37394 - Global gene expression profiles in ovarian cancer linked to Lynch syndrome

Released on 14 October 2013, last updated on 2 June 2014
Homo sapiens
Samples (67)
Array (1)
Protocols (5)
Heredity is a major cause of ovarian cancer. Lynch syndrome is associated with 10-12% risk of ovarian cancer, diagnosis at young age and a predilection for endometrioid and clear cell tumors. Global gene expression profiling applied to 25 Lynch syndrome-associated and 42 sporadic ovarian cancers revealed 335 differentially expressed genes and involvement of the mTOR and the MAPK/ERK pathways. The clear cell tumors had distinct expression profiles with upregulation of HER2 and apoptosis signaling pathways. The distinct expression profiles provide clues relevant for hereditary tumorigenesis and may be relevant for therapeutic strategies and refined diagnostics in ovarian cancer linked to Lynch syndrome. Ovarian cancers linked to Lynch syndrome (n=25) were compared to a matched series of sporadic ovarian cancers (n=42), selected from a population-based consecutive series in which hereditary was excluded based on family history, normal MMR protein staining and lack of mutations in BRCA1 and BRCA2.
Experiment type
transcription profiling by array 
Katarina Bartuma <katarina.bartuma@med.lu.se>, Ana Carneiro, Anna Måsbäck, Göran Jönsson, Jenny-Maria Jönsson, Katja Harbst, Mats Jönsson, Mef Nilbert, Mev Cominguez-Valentin, Susanne Malander, Zohreh Ketabi
Investigation descriptionE-GEOD-37394.idf.txt
Sample and data relationshipE-GEOD-37394.sdrf.txt
Processed data (1)E-GEOD-37394.processed.1.zip
Additional data (1)E-GEOD-37394.additional.1.zip
Array designA-MEXP-1564.adf.txt