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将血清蛋白和 microRNA 作为早期宫颈癌检测的新型生物标志物。

Applying Serum Proteins and MicroRNA as Novel Biomarkers for Early-Stage Cervical Cancer Detection.

机构信息

Department of Obstetrics and Gynecology, Jinan People's Hospital Affiliated to Shandong First Medical University, No. 001 Xuehu Street at Northern Changshao Road, Laiwu District, Jinan, Shandong, 271199, China.

出版信息

Sci Rep. 2020 Jun 3;10(1):9033. doi: 10.1038/s41598-020-65850-z.

Abstract

Recently, we have been seeing emerging applications of non-invasive approaches using serum biomarkers including miRNA and proteins in detection of multiple cancers. Currently, majority of these methods only use solitary type of biomarkers, which often lead to non-satisfactory sensitivity and specificity in clinical applications. To this end, we established a unique biomarker panel in this study, which determined both squamous cell carcinoma antigen (SCC Ag) degree and miRNA-29a, miRNA-25, miRNA-486-5p levels in blood for detection of early-stage cervical cancer. We designed our study with two phases: a biomarker discovery phase, followed by an independent validation phase. In total of 140 early-stage cervical cancer patients (i.e., AJCC stage I and II) and 140 healthy controls recruited in the biomarker discovery phase, we achieved sensitivity of 88.6% and specificity of 92.9%. To further assess the predictive power of our panel, we used it to an independent patient cohort that consisted of 60 early-stage cervical cancer individuals as well as 60 healthy controls, and successfully achieved both high sensitivity (80.0%) and high specificity (96.7%). Our study indicated combining analyses of multiple serum biomarkers could improve the accuracy of non-invasive detection of early-stage cervical cancer, and potentially serve as a new liquid biopsy approach for detecting early-stage cervical cancer.

摘要

最近,我们已经看到了使用血清生物标志物(包括 miRNA 和蛋白质)进行多种癌症检测的无创方法的新兴应用。目前,这些方法大多数仅使用单一类型的生物标志物,这在临床应用中往往导致不理想的敏感性和特异性。为此,我们在这项研究中建立了一个独特的生物标志物组合,用于检测早期宫颈癌,该组合同时测定了血液中的鳞状细胞癌抗原(SCCAg)程度和 miRNA-29a、miRNA-25、miRNA-486-5p 水平。我们的研究设计分为两个阶段:生物标志物发现阶段和独立验证阶段。在生物标志物发现阶段,共招募了 140 名早期宫颈癌患者(即 AJCC Ⅰ期和Ⅱ期)和 140 名健康对照者,我们实现了 88.6%的敏感性和 92.9%的特异性。为了进一步评估我们的组合的预测能力,我们将其用于包含 60 名早期宫颈癌患者和 60 名健康对照者的独立患者队列中,成功实现了 80.0%的高敏感性和 96.7%的高特异性。我们的研究表明,结合分析多种血清生物标志物可以提高早期宫颈癌无创检测的准确性,并可能成为检测早期宫颈癌的新液体活检方法。

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