Department of Gynecologic Cancer, Shaanxi Provincial Cancer Hospital, No. 309 Yanta West Road, Shaanxi, 710061, Xi'an, People's Republic of China.
Department of Obstetrics and Gynecology, Shaanxi Provincial Rehabilitation Hospital, Xi'an, Shaanxi, People's Republic of China.
J Ovarian Res. 2022 May 6;15(1):54. doi: 10.1186/s13048-022-00980-8.
Ovarian cancer (OVC) is a devastating disease worldwide; therefore the identification of prognostic biomarkers is urgently needed. We aimed to determine a robust microRNA signature-based risk score system that could predict the overall survival (OS) of patients with OVC.
We extracted the microRNA expression profiles and corresponding clinical data of 467 OVC patients from The Cancer Genome Atlas (TCGA) database and further divided this data into training, validation and complete cohorts. The key prognostic microRNAs for OVC were identified and evaluated by robust likelihood-based survival analysis (RLSA) and multivariable Cox regression. Time-dependent receiver operating characteristic (ROC) curves were then constructed to evaluate the prognostic performance of these microRNAs. A total of 172 ovarian cancer samples and 162 normal ovarian tissues were used to verify the credibility and accuracy of the selected markers of the TCGA cohort by quantitative real-time polymerase chain reaction (PCR).
We successfully established a risk score system based on a six-microRNA signature (hsa-miR-3074-5p, hsa-miR-758-3p, hsa-miR-877-5p, hsa-miR-760, hsa-miR-342-5p, and hsa-miR-6509-5p). This microRNA based system is able to characterize patients as either high or low risk. The OS of OVC patients, with either high or low risk, was significantly different when compared in the training cohort (p < 0.001), the validation cohort (p < 0.001) and the complete cohort (p < 0.001). Analysis of clinical samples further demonstrated that these microRNAs were aberrantly expressed in OVC tissues. The six-miRNA-based signature was correlated with the prognosis of OVC patients (p < 0.001).
The study established a novel risk score system that is predictive of patient prognosis and is a potentially useful guide for the personalized treatment of OVC patients.
卵巢癌(OVC)是一种全球性的毁灭性疾病;因此,迫切需要确定预后生物标志物。我们旨在确定一种基于稳健微 RNA 特征的风险评分系统,该系统可以预测 OVC 患者的总生存期(OS)。
我们从癌症基因组图谱(TCGA)数据库中提取了 467 名 OVC 患者的微 RNA 表达谱和相应的临床数据,并进一步将该数据分为训练、验证和完整队列。通过稳健似然生存分析(RLSA)和多变量 Cox 回归确定并评估关键的 OVC 预后微 RNA。然后构建时间依赖性接收者操作特征(ROC)曲线以评估这些微 RNA 的预后性能。使用定量实时聚合酶链反应(PCR)验证 TCGA 队列中选定标志物的可信度和准确性,共验证了 172 例卵巢癌样本和 162 例正常卵巢组织。
我们成功地建立了一个基于六个微 RNA 特征(hsa-miR-3074-5p、hsa-miR-758-3p、hsa-miR-877-5p、hsa-miR-760、hsa-miR-342-5p 和 hsa-miR-6509-5p)的风险评分系统。该微 RNA 系统能够将患者分为高风险或低风险。在训练队列(p<0.001)、验证队列(p<0.001)和完整队列(p<0.001)中,OVC 患者的 OS 存在显著差异。对临床样本的分析进一步表明,这些微 RNA 在 OVC 组织中异常表达。基于六个微 RNA 的特征与 OVC 患者的预后相关(p<0.001)。
本研究建立了一种新的风险评分系统,可预测患者的预后,是为 OVC 患者提供个性化治疗的潜在有用指南。