Molecular profiling and clinical outcome of high-grade serous ovarian cancer presenting with low- versus high-volume ascites.
Tomer FeigenbergBlaise ClarkeCarl VirtanenAnna PlotkinMichelle LetarteBarry RosenMarcus Q BernardiniAlexandra KollaraTheodore J BrownK Joan MurphyPublished in: BioMed research international (2014)
Epithelial ovarian cancer consists of multiple histotypes differing in etiology and clinical course. The most prevalent histotype is high-grade serous ovarian cancer (HGSOC), which often presents at an advanced stage frequently accompanied with high-volume ascites. While some studies suggest that ascites is associated with poor clinical outcome, most reports have not differentiated between histological subtypes or tumor grade. We compared genome-wide gene expression profiles from a discovery cohort of ten patients diagnosed with stages III-IV HGSOC with high-volume ascites and nine patients with low-volume ascites. An upregulation of immune response genes was detected in tumors from patients presenting with low-volume ascites relative to those with high-volume ascites. Immunohistochemical studies performed on tissue microarrays confirmed higher expression of proteins encoded by immune response genes and increased tumorinfiltrating cells in tumors associated with low-volume ascites. Comparison of 149 advanced-stage HGSOC cases with differential ascites volume at time of primary surgery indicated low-volume ascites correlated with better surgical outcome and longer overall survival. These findings suggest that advanced stage HGSOC presenting with low-volume ascites reflects a unique subgroup of HGSOC, which is associated with upregulation of immune related genes, more abundant tumor infiltrating cells and better clinical outcomes.
Keyphrases
- cell free
- high grade
- genome wide
- immune response
- poor prognosis
- induced apoptosis
- cell proliferation
- small molecule
- low grade
- dna methylation
- dendritic cells
- randomized controlled trial
- cell cycle arrest
- newly diagnosed
- minimally invasive
- toll like receptor
- gene expression
- cell death
- acute coronary syndrome
- genome wide identification
- case control
- binding protein