Figure 1.

Flow chart of our study design. miRNA profiling was performed using TaqMan PCR in a homogenous set of 3 primary advanced and 3 recurrent serous papillary ovarian adenocarcinomas from different patients. Selected miRNA targets (n = 2) were examined in two independent sets of primary and recurrent fresh frozen (n = 18) and FFPE serous papillary adenocarcinomas (n = 22). We also attempted to determine whether components of the miRNA processing machinery (Dicer and Drosha) are responsible for miRNA dysregulation in recurrent ovarian cancer.

Laios et al. Molecular Cancer 2008 7:35   doi:10.1186/1476-4598-7-35
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