MicroRNA 21在子宫内膜癌和良性病变中的诊断价值及其与临床病理参数的差异表达。

Amal Bouziyane, Maryame Lamsisi, Hicham Benaguida, Mustapha Benhessou, Mohamed El Kerroumi, Moulay Mustapha Ennaji
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引用次数: 3

摘要

背景:子宫内膜癌是全球女性最常见的恶性肿瘤之一。虽然这种癌症通常在早期阶段被诊断出来,但对诊断的生物标志物的需求仍然是克服传统侵入性诊断程序的必要条件。目的:探讨microRNA-21在子宫内膜癌中的诊断价值及其与临床病理特征的关系。方法:采用RT-qPCR检测71例肿瘤组织、53例癌旁组织和54例良性病变组织中microRNA-21的表达。结果:我们的研究结果表明,miR-21是子宫内膜癌的潜在生物标志物,其受体工作特征曲线下面积为0.925 (95% CI = 0.863 ~ 0.964)。结论:我们的研究结果支持miR-21作为子宫内膜癌诊断的生物标志物的重要作用。进一步研究微创/无创样本如血清、血液和尿液是必要的,以提供更好的替代现有的诊断方法。
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Diagnostic Value of MicroRNA 21 in Endometrial Cancer and Benign Lesions and its Differential Expression with Clinicopathological Parameters.

Background: Endometrial cancer is one of the most common malignancies among women worldwide. Although this cancer is often diagnosed at early stages, the need for biomarkers of diagnosis remains a necessity to overcome conventional invasive procedures of diagnosis.

Objective: In our study, we aim to investigate the diagnostic value of microRNA-21 in endometrial cancer and its relation to clinicopathological features.

Methods: We used RT-qPCR to measure the expression of microRNA-21 in 71 tumor tissues, 53 adjacent tissues, and 54 benign lesions.

Results: Our results show that microRNA-21 is a potential biomarker for endometrial cancer with an area under the receiver operating characteristic curve of 0.925 (95% CI = 0.863 - 0.964, P<0.0001). The sensitivity was 84.51% (95% CI = 74.0 - 92.0) and specificity was 86.79% (95% CI = 74.7 - 94.5). For discrimination between benign lesions and controls the AUC was 0,881 with a sensitivity of 100% (95% CI = 93.4 - 100.0) and specificity of 66.04% (95% CI = 51.7 - 78.5), and for discriminating benign lesions from tumors the AUC was 0,750 with a sensitivity of 54.93% (95% CI = 42.7 - 66.8) and specificity of 90.74% (95% CI = 79.7 - 96.9). We also found that tumors with elevated microRNA-21 expression are of advanced FIGO stage, high histological grades, and have cervical invasion, myometrial invasion and distant metastasis.

Conclusion: Our findings support the important role of miR-21 as a biomarker to diagnose endometrial cancer. Further studies on minimally invasive/noninvasive samples such as serum, blood, and urine are necessary to provide a better alternative to current diagnosis methods.

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