Abstract
Objective: To determine the utility of serum miRNAs as biomarkers for epithelial ovarian cancer. Methods: Twenty-eight patients with histologically confirmed epithelial ovarian cancer were identified from a tissue and serum bank. Serum was collected prior to definitive therapy. Fifteen unmatched, healthy controls were used for comparison. Serum was obtained from all patients. RNA was extracted using a derivation of the single step Trizol method. The RNA from 9 cancer specimens was compared to 4 normal specimens with real-time PCR using the TaqMan Array Human MicroRNA panel. Twenty-one miRNAs were differentially expressed between normal and patient serum. Real-time PCR for the 21 individual miRNAs was performed on the remaining 19 cancer specimens and 11 normal specimens. Results: Eight miRNAs of the original twenty-one were identified that were significantly differentially expressed between cancer and normal specimens using the comparative Ct method. MiRNAs-21, 92, 93, 126 and 29a were significantly over-expressed in the serum from cancer patients compared to controls (p < .01). MiRNAs-155, 127 and 99b were significantly under-expressed (p < .01). Additionally, miRs-21, 92 and 93 were over-expressed in 3 patients with normal pre-operative CA-125. Conclusion: We demonstrate that the extraction of RNA and subsequent identification of miRNAs from the serum of individuals diagnosed with ovarian cancer is feasible. Real-time PCR-based microarray is a novel and practical means to performing high-throughput investigation of serum RNA samples. miRNAs-21, 92 and 93 are known oncogenes with therapeutic and biomarker potential.
Original language | English (US) |
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Pages (from-to) | 55-59 |
Number of pages | 5 |
Journal | Gynecologic oncology |
Volume | 112 |
Issue number | 1 |
DOIs | |
State | Published - Jan 2009 |
Keywords
- Biomarkers
- MicroRNA
- Ovarian cancer
ASJC Scopus subject areas
- Oncology
- Obstetrics and Gynecology