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MicroRNA expression profiles in non‑epithelial ovarian tumors.
Roger K Chang1, Xidan Li2, Ninni Mu1
1Department of Oncology-Pathology, Karolinska Institutet, Cancer Center Karolinska, Karolinska University Hospital, SE-171 76 Stockholm, Sweden.
International Journal of Oncology
|November 16, 2017
Summary
This study investigated microRNA (miRNA) expression in rare ovarian germ cell tumors (OGCTs) and sex cord stromal tumors (SCSTs). Specific miRNA profiles, like higher miR-373-3p in malignant OGCTs, may serve as ovarian cancer biomarkers.
Area of Science:
- Gynecologic Oncology
- Molecular Pathology
- Genomics
Background:
- Ovarian germ cell tumors (OGCTs) and sex cord stromal tumors (SCSTs) are rare gynecologic neoplasms.
- Their molecular pathogenesis remains poorly understood compared to epithelial ovarian cancers.
Purpose of the Study:
- To characterize microRNA (miRNA) expression profiles in OGCTs and SCSTs.
- To identify potential miRNA biomarkers for distinguishing tumor types and malignancy.
Main Methods:
- Small RNA sequencing was used to analyze miRNA expression in 9 OGCTs and 3 SCSTs.
- Quantitative reverse transcription PCR validated miRNA expression in an extended cohort (16 OGCTs, 7 SCSTs).
- Western blot analysis assessed Beclin 1 (BECN1) expression in relation to miRNA levels.
Main Results:
- Significant miRNA expression variations were observed across OGCTs and SCSTs.
- Malignant OGCTs showed higher expression of miR-373-3p, miR-372-3p, miR-302c-3p and lower expression of miR-199a-5p, miR-214-5p, miR-202-3p compared to benign OGCTs or SCSTs.
- SCSTs exhibited higher miR-202c-3p and miR-513c-5p than benign OGCTs. BECN1 expression was elevated in malignant OGCTs, inversely correlating with miR-199a-5p levels.
Conclusions:
- Specific miRNA signatures differentiate OGCTs and SCSTs, and correlate with malignancy in OGCTs.
- These miRNAs hold potential as diagnostic biomarkers for ovarian tumors.
- The findings offer insights into the molecular mechanisms underlying OGCT and SCST development.
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