Delek Fatma Seher Pektopal, Tunçer Şeref Buğra, Ödemiş Demet Akdeniz, Erciyas Seda Kılıç, Erdoğan Özge Şükrüoğlu, Saip Pınar, Yazıcı Hülya
Division of Cancer Genetics, Department of Basic Oncology, Oncology Institute, Istanbul University, Çapa-Fatih, 34093, Istanbul, Türkiye.
Division of Cancer Genetics, Department of Basic Oncology, Institute of Health Sciences, Istanbul University, Vezneciler-Fatih, 32416, Istanbul, Türkiye.
Biochem Genet. 2024 May 5. doi: 10.1007/s10528-024-10819-0.
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 < 0.001). In addition, receiver-operating characteristic curve analysis of PBMC showed statistical significance of miR-3653-3p in discriminating ovarian cancer patients from healthy subjects (P < 0.001). These results suggest that miR-3653-3p detected in peripheral blood may be used as a non-invasive biomarker for ovarian cancer.
卵巢癌通常在晚期被诊断出来,早期经常复发,目前缺乏有效的治疗方法。因此,这种疾病的总生存期和无进展生存期相对较短。目前缺乏用于该疾病早期诊断和有效治疗随访的敏感且特异的生物标志物。微小RNA(miRNA/miR)表达研究广泛应用于癌症研究。一类非编码小RNA即miRNA的破坏或功能失调在一些出版物中被认为与癌症进展有关。值得注意的是,已知一系列miRNA的表达在卵巢癌中存在差异。在癌症研究中,分析癌症患者和健康个体的表达模式对于识别癌症特异性生物标志物并了解其在癌症中的作用至关重要。在本研究中,测定了150例高危卵巢癌患者外周血单个核细胞(PBMC)中miR-3653-3p的表达水平,这些患者包括有癌症家族史或早期诊断为卵巢癌的患者,以及100名健康个体。然后比较两组的结果。卵巢癌患者PBMC中miR-3653-3p的表达水平被确定比健康对照组高9.49倍,且该结果具有统计学意义(P < 0.001)。此外,PBMC的受试者工作特征曲线分析表明,miR-3653-3p在区分卵巢癌患者和健康受试者方面具有统计学意义(P < 0.001)。这些结果表明,在外周血中检测到的miR-3653-3p可能用作卵巢癌的非侵入性生物标志物。