miR-3653-3p Expression in PBMCs: Unveiling the Diagnostic Potential for Ovarian Cancer

Ovarian cancer is typically diagnosed at an advanced stage, recurs early and often, and currently lacks effective treatment. Therefore, overall survival and progression-free survival are relatively short for this disease. Sensitive and specific biomarkers for early diagnosis and follow-up for effect...

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Veröffentlicht in:Biochemical genetics 2024-05
Hauptverfasser: Delek, Fatma Seher Pektopal, Tunçer, Şeref Buğra, Ödemiş, Demet Akdeniz, Erciyas, Seda Kılıç, Erdoğan, Özge Şükrüoğlu, Saip, Pınar, Yazıcı, Hülya
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Sprache:eng
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Zusammenfassung:Ovarian cancer is typically diagnosed at an advanced stage, recurs early and often, and currently lacks effective treatment. Therefore, overall survival and progression-free survival are relatively short for this disease. Sensitive and specific biomarkers for early diagnosis and follow-up for effective treatment of the disease are currently lacking. MicroRNA (miRNA/miR) expression studies are widely used in cancer research. Disruption or malfunction of miRNAs, a class of noncoding small RNAs, has been implicated in cancer progression in several publications. Of note, the expression of a series of miRNAs is known to differ in ovarian cancer. In cancer research, it is crucial to analyze expression patterns in both cancer patients and healthy individuals to identify cancer-specific biological markers and to understand their role in cancer. In the present study, the expression levels of miR-3653-3p in the peripheral blood mononuclear cells (PBMCs) of 150 patients with high-risk ovarian cancer were determined, including those with a family history of cancer or an early-age diagnosis of ovarian cancer, as well as 100 healthy individuals. The results were then compared between the two groups. The expression level of miR-3653-3p in the PBMCs of patients with ovarian cancer was determined to be 9.49-fold higher than that in the healthy control group, and this result was statistically significant (P 
ISSN:0006-2928
1573-4927
DOI:10.1007/s10528-024-10819-0